[go: up one dir, main page]

US20190248852A1 - MIC-1 Compounds and Use Thereof - Google Patents

MIC-1 Compounds and Use Thereof Download PDF

Info

Publication number
US20190248852A1
US20190248852A1 US16/303,516 US201716303516A US2019248852A1 US 20190248852 A1 US20190248852 A1 US 20190248852A1 US 201716303516 A US201716303516 A US 201716303516A US 2019248852 A1 US2019248852 A1 US 2019248852A1
Authority
US
United States
Prior art keywords
seq
mic
amino acid
compound according
compound
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US16/303,516
Other languages
English (en)
Inventor
Xujia Zhang
Xiang Gao
Hongtao Guan
Henning Thoegersen
Kristian Sass-Oerum
Lars Fogh Iversen
Per Noergaard
Sebastian Beck Joergensen
Kristian Tage Hansen
Yi Wang
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Novo Nordisk AS
Original Assignee
Novo Nordisk AS
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Novo Nordisk AS filed Critical Novo Nordisk AS
Assigned to NOVO NORDISK A/S reassignment NOVO NORDISK A/S ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: ZHANG, XUJIA, GAO, XIANG, THOEGERSEN, HENNING, WANG, YI, HANSEN, KRISTIAN TAGE, IVERSEN, LARS FOGH, JOERGENSEN, SEBASTIAN BECK, NOERGAARD, PER, GUAN, Hongtao, SASS-OERUM, KRISTIAN
Publication of US20190248852A1 publication Critical patent/US20190248852A1/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/475—Growth factors; Growth regulators
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/475—Growth factors; Growth regulators
    • C07K14/495—Transforming growth factor [TGF]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • A61K38/18—Growth factors; Growth regulators
    • A61K38/1841—Transforming growth factor [TGF]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • A61K38/19—Cytokines; Lymphokines; Interferons
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • A61K38/22—Hormones
    • A61K38/27—Growth hormone [GH], i.e. somatotropin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/62—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being a protein, peptide or polyamino acid
    • A61K47/64—Drug-peptide, drug-protein or drug-polyamino acid conjugates, i.e. the modifying agent being a peptide, protein or polyamino acid which is covalently bonded or complexed to a therapeutically active agent
    • A61K47/642—Drug-peptide, drug-protein or drug-polyamino acid conjugates, i.e. the modifying agent being a peptide, protein or polyamino acid which is covalently bonded or complexed to a therapeutically active agent the peptide or protein in the drug conjugate being a cytokine, e.g. IL2, chemokine, growth factors or interferons being the inactive part of the conjugate
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/04—Anorexiants; Antiobesity agents
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/10—Tetrapeptides
    • C07K5/1002—Tetrapeptides with the first amino acid being neutral
    • C07K5/1005—Tetrapeptides with the first amino acid being neutral and aliphatic
    • C07K5/1008—Tetrapeptides with the first amino acid being neutral and aliphatic the side chain containing 0 or 1 carbon atoms, i.e. Gly, Ala
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/10—Tetrapeptides
    • C07K5/1002—Tetrapeptides with the first amino acid being neutral
    • C07K5/1005—Tetrapeptides with the first amino acid being neutral and aliphatic
    • C07K5/1013—Tetrapeptides with the first amino acid being neutral and aliphatic the side chain containing O or S as heteroatoms, e.g. Cys, Ser
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
    • C07K7/04—Linear peptides containing only normal peptide links
    • C07K7/06—Linear peptides containing only normal peptide links having 5 to 11 amino acids
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
    • C07K7/04—Linear peptides containing only normal peptide links
    • C07K7/08—Linear peptides containing only normal peptide links having 12 to 20 amino acids
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2319/00—Fusion polypeptide
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2319/00—Fusion polypeptide
    • C07K2319/31—Fusion polypeptide fusions, other than Fc, for prolonged plasma life, e.g. albumin

Definitions

  • the present invention relates to MIC-1 compounds and their pharmaceutical use.
  • MIC-1 Macrophage Inhibitory Cytokine-1 (MIC-1) was first described in 1997 (Bootcov et al, Proc. Natl. Acad. Sci. October 1997) based on experiments showing increased expression in activated macrophages. MIC-1 has subsequently been identified by others and given several additional names such as placental transforming growth factor beta (PTGF- ⁇ ), placental bone morphogenetic protein, growth differentiation factor-15 (GDF15), prostate derived factor (PDF), non-steroidal anti-inflammatory drug-activated gene (NAG-1) and PL74.
  • PTGF- ⁇ placental transforming growth factor beta
  • GDF15 growth differentiation factor-15
  • PDF prostate derived factor
  • NAG-1 non-steroidal anti-inflammatory drug-activated gene
  • MIC-1 is a distant member of the TGF-beta super family, a family of peptide hormones involved in cell growth and differentiation. MIC-1 circulates as a cysteine-rich homodimer with a molecular mass of 24.5 kDa. MIC-1 was initially reported to be up-regulated in macrophages by stimuli including IL-1b, TNF-alpha, IL-2, and TGF-b. It was also shown that MIC-1 could reduce lipopolysaccharide-induced TNF-alpha production and it was based on these data proposed that MIC-1 was an anti-inflammatory cytokine.
  • transgenic mice overexpressing MIC-1 are gaining less weight and body fat both on a normal low fat diet and on a high fat diet (Macia et al, PLoS One, April 2012). Also, transgenic mice overexpressing MIC-1 fed both on a low and high fat diet, respectively, had improved glucose tolerance compared with wild type animals on a comparable diet.
  • Obesity is most commonly caused by excessive calorie intake alone or in conjunction with decreased energy expenditure and/or lack of physical exercise. Obesity is a well-established risk factor for metabolic diseases like diabetes, cardiovascular diseases, sleep apnea and cancer.
  • MIC-1 compounds comprising MIC-1 polypeptides with N-terminal amino acid extensions.
  • the MIC-1 compounds of the invention have good biophysical properties. These properties include but are not limited to solubility and stability. In one aspect, the MIC-1 compounds of the invention have improved solubility. In one aspect, the MIC-1 compounds of the invention have improved chemical stability.
  • the compounds of the invention have improved biophysical stability as shown by reduced crystal forming tendency.
  • the MIC-1 compounds of the invention have retained MIC-1 receptor potency and in vivo efficacy on lowering food intake and body weight. These MIC-1 compounds can therefore be used for treatment of metabolic disorders such as obesity, diabetes, cardiovascular diseases like dyslipidaemia and arteriosclerosis and other disorders such as steatohepatitis and diabetic nephropathy.
  • the MIC-1 compounds of the invention comprises a MIC-1 polypeptide and an N-terminal amino acid extension, wherein said extension consists of 3 to 36 amino acid residues and where the compound has a calculated pI lower than 6.5.
  • the MIC-1 compound has a calculated pI that is lower than 6.1.
  • the MIC-1 compound has a calculated pI that is higher than 4.7.
  • the MIC-1 compound has a calculated pI that is higher than 4.7 and lower than 6.1.
  • the MIC-1 compound has a calculated pI is in the range of 5.8-5.2.
  • the MIC-1 compounds of the invention as homodimers, have between 218-296, 224-296 or 230-296 amino acid residues.
  • the MIC-1 compounds of the invention comprise an N-terminal extension that is in the range of 3-35, 3-30, 3-25, 3-24, 4-36, 4-35, 4-30, 4-25, 4-24, 5-36, 5-35, 5-30, 5-25, 5-24, 6-36, 6-35, 6-30, 6-25, 6-24, 7-36, 7-35, 7-30, 7-25, 7-24, 8-36, 8-35, 8-30, 8-25, 8-24, 8-12, 30-36, 32-36, 30-34, or 30-32 amino acid residues in length.
  • the MIC-1 compounds of the invention comprise an N-terminal extension that is in the range of 30-32 amino acid residues in length.
  • the MIC-1 compounds of the invention comprise an N-terminal extension that has surplus of acidic amino acid residues (Aspartic acid and Glutamic acid) of at least 3, 4, 5 or 6 compared to the number of basic amino acid residues (Lysine, Arginine and Histidine).
  • the MIC-1 compounds comprise N-terminal extensions composed of amino acid residues selected among the group consisting of A, E, G, P, S, T, Q, and D wherein said extension comprises at least three E and/or D amino acid residues.
  • the MIC-1 compounds of the invention comprise an MIC-1 polypeptide that display at least 85%, 90%, 95% or 98% sequence identity to MIC-1 of SEQ ID NO:1.
  • the MIC-1 compounds of the invention comprise an MIC-1 polypeptide that comprises one or more of the following substitutions N3E, P11E, H18E, R21E, A30E, A47E, R53E, A54E, M57E, M57L, R67E, L68E, K69E, A75E, A81E, P85E, M86L, L105E, and K107E compared to MIC-1 of SEQ ID NO:1 and/or a deletion of the first three residues (MIC-1- ⁇ 1-3) or a deletion of N3 (des-N3) compared to MIC-1 of SEQ ID NO:1.
  • the MIC-1 compound comprises a MIC-1 polypeptide and an N-terminal amino acid extension with an amino acid sequence according to SEQ ID NO: 87, 90, 92, 93, 94, 97, 98, 99, 100, 101, 102, 108, 109, or 164.
  • the invention provides MIC-1 compounds having a solubility of about 0.5, 1.0, 5.0, 10, 30 or 50 mg/ml at pH 8.0 in a tris(hydroxymethyl)aminomethane (Tris) buffer system.
  • Tris tris(hydroxymethyl)aminomethane
  • the invention provides a polynucleotide molecule encoding a MIC-1 compound of the invention.
  • the invention provides a pharmaceutical composition
  • a pharmaceutical composition comprising the MIC-1 compound of the invention or a pharmaceutically acceptable salt, amide or ester thereof, and one or more pharmaceutically acceptable excipients.
  • the invention provides a MIC-1 compound of the invention for use as a medicament.
  • the invention provides a MIC-1 compound of the invention for use in the prevention and/or treatment of a metabolic disorder, wherein the metabolic disorder is obesity, type 2 diabetes, dyslipidemia, or diabetic nephropathy.
  • the invention provides a MIC-1 compound of the invention for use in the prevention and/or treatment of eating disorders, such as obesity, e.g. by decreasing food intake, reducing body weight, suppressing appetite and inducing satiety.
  • eating disorders such as obesity, e.g. by decreasing food intake, reducing body weight, suppressing appetite and inducing satiety.
  • the invention provides a MIC-1 compound of the invention for use in the prevention and/or treatment of obesity.
  • the compounds of the invention are MIC-1 receptor agonists. In one aspect, the compounds of the invention inhibit food intake. In one aspect, the compounds of the invention reduce body weight.
  • the invention provides a MIC-1 compound of the invention for use in the prevention and/or treatment of a cardiovascular disease.
  • the invention provides a MIC-1 compound of the invention for use in the prevention and/or treatment of dyslipidaemia, arteriosclerosis, steatohepatitis, or diabetic nephropathy.
  • FIG. 1 The expression of MIC-1 compounds with single 12-mer building blocks. All cells were grown in TB at 37° C. and proteins were induced to express by adding 0.5 mM IPTG after OD600 reached 1.0. Cells were harvested after overnight and the expression level was checked by loading the total lysate on SDS-PAGE. wtMIC-1 was loaded as the positive control.
  • FIG. 2 The expression of MIC-1 compounds with double 12-mer building blocks. All cells were grown in TB at 37° C. and proteins were induced to express by adding 0.5 mM IPTG after OD600 reached 1.0. Cells were harvested after overnight and the expression level was checked by loading the total lysate on SDS-PAGE. wtMIC-1 was loaded as the positive control.
  • FIG. 3 a) comparison of expression levels among MIC-1 compounds initiating with 12mer-(4+2+_), -(4+4+_) and -(4+3+_). It should be noticed that the group bearing 12mer-(4+3_) and the construct indicated by the dot contain M57L in the backbone of MIC-1. b) the effects of the extended 12mers on the expression level. In addition, the lowest data point in the group of 3.6 is the MIC-1 compound containing M57L. In this figure, “1.6 latter” represents TSTEEG, “2.6” represents TSESAT, “3.6” represents TSTEPS and “4.6” represents SEPATS.
  • FIG. 4 SDS-PAGE of representatives bearing 12mer-(4+2+_), 12mer-(4+3+_)+M57L, 12mer-(three repeats) and 12mer-(four repeats).
  • T total protein
  • S soluble fraction
  • P cell pellet (inclusion body).
  • FIG. 5 Solubility of MIC-1 compounds with in-sequence mutations.
  • the backbone is MIC-1 del(1-3).
  • the invention relates to a MIC-1 compound comprising a MIC-1 polypeptide.
  • the invention relates to a MIC-1 compound comprising a MIC-1 polypeptide and an N-terminal amino acid extension, wherein said extension consists of 3 to 200 amino acid residues and where the compound has a calculated pI lower than 6.5.
  • MIC-1 Macrophage Inhibitory Cytokine-1 (MIC-1), also known as Growth Differentiation Factor 15 (GDF-15), placental bone morphogenetic protein (PLAB) and nonsteroidal anti-inflammatory drug-activated gene (NAG-1).
  • GDF-15 Growth Differentiation Factor 15
  • PLAB placental bone morphogenetic protein
  • NAG-1 nonsteroidal anti-inflammatory drug-activated gene
  • MIC-1 is synthesized as a 62 kDa intracellular homodimer precursor protein which subsequently is cleaved by a furin-like protease into a 24.5 kDa homodimer.
  • the sequence of the full length wild type human MIC-1 is available from the UNIPROT database with accession no. Q99988.
  • the 308 amino acid precursor sequence includes a signal peptide (amino acids 1-29), a propeptide (amino acids 30-196) and a MIC-1 monomer sequence (amino acids 197-308).
  • the 112 amino acid MIC-1 monomer sequence is included herein as SEQ ID NO:1.
  • MIC-1 monomer contains nine cysteine residues which give rise to the formation of 4 intrachain disulphide bonds and one interchain disulphide bond to create a covalently linked 24.5 kDa homodimer.
  • a naturally occurring mutation corresponding to H6D in the MIC-1 monomer sequence (SEQ ID NO:1) has been described.
  • MIC-1 compound refers to a compound comprising a MIC-1 polypeptide and an N-terminal amino acid extension.
  • the MIC-1 compound is typically in the form of a homodimer.
  • MIC-1 polypeptide refers to the human MIC-1 monomer sequence of SEQ ID NO:1 or an analogue thereof. Numerical references to particular MIC-1 residues, if not stated otherwise, refer to the 112 amino acid monomer sequence (i.e., residue 1 is Alanine (A1), and residue 112 is Isoleucine (I112).
  • MIC-1 analogue refers to a MIC-1 polypeptide, which is an amino acid variant of the monomer MIC-1 sequence of SEQ ID NO:1.
  • a MIC-1 analogue is a MIC-1 polypeptide in which a number of amino acid residues have been changed when compared to human MIC-1 (SEQ ID NO: 1). These changes may represent, independently, one or more amino acid substitutions, additions, and/or deletions.
  • MIC-1 analogues may be described by reference to the amino acid residue which is changed, the number of the amino acid residue (i.e. the corresponding position in the MIC-1 monomer sequence (SEQ ID NO:1)), and the change (e.g. the amino acid residue change to).
  • the MIC-1 analogue is a functional variant of the MIC-1 of SEQ ID NO:1.
  • the MIC-1 analogues display at least 85%, 90% or 95% sequence identity to MIC-1 of SEQ ID NO:1.
  • the two peptides H6D MIC-1 and MIC-1 of SEQ ID NO:1 are aligned.
  • the sequence identity of the H6D MIC-1 analogue relative to MIC-1 of SEQ ID NO:1 is given by the number of aligned identical residues minus the number of different residues divided by the total number of residues in MIC-1 of SEQ ID NO:1. Accordingly, in said example the sequence identity in percentage is (112-1)/112 ⁇ 100.
  • the N-terminal amino acid extension is not included.
  • the MIC-1 analogues comprise less than for example less than 15, 10 or 5, amino acid modifications (substitutions, deletions, additions (including insertions) and any combination thereof) relative to human MIC-1 of SEQ ID NO:1.
  • amino acid modification used throughout this application is used in the meaning of a modification to an amino acid as compared to monomer MIC-1 (SEQ ID NO:1). This modification can be the result of a deletion of an amino acid, addition of an amino acid, substitution of one amino acid with another or a substituent covalently attached to an amino acid of the peptide.
  • amino acids may be substituted by conservative substitution.
  • conservative substitution denotes that one or more amino acids are replaced by another, biologically similar residue. Examples include substitution of amino acid residues with similar characteristics, e.g. small amino acids, acidic amino acids, polar amino acids, basic amino acids, hydrophobic amino acids and aromatic amino acids.
  • amino acids may be substituted by non-conservative substitution.
  • non-conservative substitution denotes that one or more amino acids are replaced by another amino acid having different characteristics. Examples include substitution of a basic amino acid residue with an acidic amino acid residue, substitution of a polar amino acid residue with an aromatic amino acid residue, etc.
  • the non-conservative substitution is substitution of a coded amino acid to another coded amino acid having different characteristics.
  • the MIC-1 analogues may comprise substitutions of one or more unnatural and/or non-amino acids, e.g., amino acid mimetics, into the sequence of MIC-1.
  • the asparagine residue in position 3 (N3) of human MIC-1 monomer sequence (SEQ ID NO:1) is chemically labile.
  • the asparagine in the position corresponding to position 3 of monomer MIC-1 sequence (SEQ ID NO:1) may be substituted to Serine (N3S), Glutamic acid (N3E), Alanine (N3A), or Glutamine (N3Q).
  • the asparagine in the position corresponding to position 3 of human MIC-1 monomer sequence (SEQ ID NO:1) has been substituted to Glutamic acid (N3E).
  • the arginine in the position corresponding to position 2 of human MIC-1 monomer sequence has been substituted to alanine (R2A), and the asparagine in the position corresponding to position 3 of human MIC-1 monomer sequence (SEQ ID NO:1) has been substituted to Glutamic acid (N3E).
  • the MIC-1 analogues of the invention may have one or more amino acid residues deleted from the amino acid sequence of MIC-1 (SEQ ID NO:1), alone or in combination with one or more insertions or substitutions.
  • MIC-1 analogues with amino acid deletions may be described by “des”, reference to the amino acid residue which is deleted, and followed by the number of the deleted amino acid (i.e. the corresponding position in the monomer MIC-1 (SEQ ID NO:1)).
  • the asparagine in the position corresponding to position 3 of human monomer MIC-1 is deleted (MIC-1 des-N3, SEQ ID NO:2).
  • MIC-1 analogues with a truncation of one or more amino acid residues at the N or C terminal may be described by “MIC-1- ⁇ ” and reference to the number(s) of the deleted amino acid residues (i.e. the corresponding position in the monomer MIC-1 (SEQ ID NO:1)).
  • the first three residues (A1, R2, N3) at the N terminal are deleted (MIC-1- ⁇ 1-3, SEQ ID NO:3).
  • the MIC-1 analogues of the invention may have one or more amino acid residues inserted into the amino acid sequence of human MIC-1, alone or in combination with one or more deletions and/or substitutions.
  • the MIC-1 analogues of the invention may include insertions of one or more unnatural amino acids and/or non-amino acids into the sequence of MIC-1.
  • protein or “polypeptide”, as e.g. used herein, refers to a compound which comprises a series of amino acids interconnected by amide (or peptide) bonds.
  • Amino acids are molecules containing an amine group and a carboxylic acid group, and, optionally, one or more additional groups, often referred to as a side chain.
  • amino acid includes coded (or proteinogenic or natural) amino acids (amongst those the 20 standard amino acids), as well as non-coded (or non-proteinogenic or non-natural) amino acids. Coded amino acids are those which are naturally incorporated into proteins. The standard amino acids are those encoded by the genetic code. Non-coded amino acids are either not found in proteins, or not produced by standard cellular machinery (e.g., they may have been subject to post-translational modification). In what follows, all amino acids of the MIC-1 proteins for which the optical isomer is not stated is to be understood to mean the L-isomer (unless otherwise specified).
  • amino acid residues may be identified by their full name, their one-letter code, and/or their three-letter code. These three ways are fully equivalent.
  • amino acid codes are provided below:
  • Glycine G and Gly; Proline: P and Pro; Alanine: A and Ala; Valine: V and Val; Leucine: L and Leu; Isoleucine: I and Ile; Methionine: M and Met; Cysteine: C and Cys; Phenylalanine: F and Phe; Tyrosine: Y and Tyr; Tryptophan: W and Trp; Histidine: H and His; Lysine: K and Lys; Arginine: R and Arg; Glutamine: Q and Gin; Asparagine: N and Asn; Glutamic Acid: E and Glu; Aspartic Acid: D and Asp; Serine: S and Ser; and Threonine: T and Thr.
  • the MIC-1 compound comprises an N-terminal amino acid extension.
  • N-terminal amino acid extension means that the N-terminal of the MIC-1 polypeptide is attached to the C-terminal of the N-terminal amino acid extension via an amide bond, preferably a peptide bond.
  • the terms “N-terminal amino acid extension”, “N-terminal extension”, and “N-extension” herein means the same thing and are used interchangeably.
  • the compound of the invention comprises human MIC-1 monomer sequence (SEQ ID NO:1) with an amino acid extension attached at the N-terminal, i.e. the Alanine at positon 1 (A1) via a peptide bond.
  • the N-terminal amino acid extension is up to 200 amino acid residues long. In a particular embodiment of the invention the N-terminal amino acid extension has from 3 to 36 amino acid residues.
  • the N-terminal amino acid extension has a surplus of acidic amino acid residues (Aspartic acid and Glutamic acid) of at least 3, 4, 5 or 6 compared to the number of basic amino acid residues (Lysine, Arginine and Histidine).
  • a “surplus” of acidic amino acid residues means that the number of acidic residues exceeds the number of basic residues.
  • a defined value of the surplus of acidic amino acid residues is calculated as the number of acidic residues minus the number of basic residues.
  • Methionine is the initial amino acid for protein expression in prokaryotic cells (e.g. bacteria, for instance, E.coli ).
  • the initial Methionine is removed from the protein during the protein expression. Therefore, the initial Methionine is not included in the sequence of the N-extension of MIC-1 compound.
  • the start codon, coding the initial Methionine is required for the protein translation initiation and should be incorporated right in front of the nucleotide sequence for protein expression without exception.
  • the calculated pI of a MIC-1 compound is defined as the pH at which the net calculated charge of the compound is zero.
  • the calculated charge of the MIC-1 compound as a function of pH is obtained using the pKa values of the amino acid residues described in Table 1 and the method described by B. Skoog and A. Wichman (Trends in Analytical Chemistry, 1986, vol. 5, pp. 82-83).
  • the side chain pKa of cysteine (Cys) is only included in the charge calculation for cysteines with a free sulfhydryl group.
  • the calculated pI value of human wtMIC-1 is 8.8 as the homodimer.
  • pKa of amino acid residues used for calculating pI are those described in “Correlation of Electrophoretic Mobilities from Capillary Electrophoresis with Physicochemical Properties of Proteins and Peptides by Rickard E C, Strohl M M, Nielsen R G. Analytical Biochemistry 1991, vol 197, pp 197-207”.
  • the MIC-1 compounds of the invention have good biophysical properties. These properties include but are not limited to solubility and/or stability.
  • the human wild type MIC-1 is a hydrophobic protein, with a calculated pI 8.8 based on the homodimer. Consequently, wild type MIC-1 can only be solubilized to around 0.5 mg/ml in neutral pH aqueous buffer systems. The low solubility of MIC-1 significantly hampers its formulation properties and therapeutic use, so developing a solubility-engineered MIC-1 compound is important for MIC-1 molecular engineering.
  • the compounds of the invention have improved solubility (i.e. are more soluble) relative to human MIC-1 of SEQ ID NO:1.
  • solubility is measured as described in Example 4.
  • the MIC-1 compounds of the invention have a solubility of at least 1 mg/ml in Tris buffer at pH 8.0. In other embodiments, the compounds of the invention have a solubility of at least 5 mg/ml, at least 10 mg/ml, at least 30 mg/ml, or at least 40 mg/ml in Tris buffer at pH 8.0.
  • solubility is measured on MIC-1 compounds as homodimers.
  • the human wild type MIC-1 sequence is a chemically instable and several residues of the amino acid sequence could be modified during storage, including deamidation on Asparagine at position 3 (N3) and oxidation of methionines M43, M57 and M86. Chemical instability of certain residues could impact pharmaceutical properties so developing chemical stable MIC-1 compounds would be another important part of making a MIC-1 therapeutic compound.
  • the compounds of the invention have improved chemical stability relative to human MIC-1 of SEQ ID NO:1.
  • chemical stability refers to chemical changes in the polypeptide structure leading to formation of chemical degradation products potentially having a reduced biological activity, decreased solubility, and/or increased immunogenic effect as compared to the intact polypeptide.
  • the chemical stability can be evaluated by measuring the amount of chemical degradation products at various time-points after exposure to different environmental conditions, e.g. by SEC-HPLC, and/or RP-HPLC.
  • certain residues of the MIC-1 monomer sequence is modified, e.g. by substitution to increase the chemical stability of the MIC-1 compounds.
  • N3 could be deleted or substituted with other amino acids, e.g. E or Q.
  • Methionine could be substituted with other amino acids, e.g. E or L.
  • the compounds of the invention have low immunogenicity risk.
  • the compounds of the invention have retained MIC-1 receptor potency relative to human MIC-1 (SEQ ID NO:1).
  • Receptor potency and efficacy can be measured in mammalian cells transfected with human MIC-1 receptor (hGFRAL, GDNF family receptor alpha like) and its signalling co-receptor hRET51 (proto-oncogene tyrosine-protein kinase receptor Ret isoform 51).
  • MIC-1 compounds activation of the receptor complex is measured by phosphorylation of extracellular signal-regulated kinases (ERKs) as described in Example 6.
  • ERKs extracellular signal-regulated kinases
  • receptor potency and efficacy is measured on MIC-1 compounds as homodimers.
  • the compounds of the invention are potent in vivo, which may be determined as is known in the art in any suitable animal model.
  • the non-obese Sprague Dawley rat is one example of a suitable animal model, and the changes in food intake may be determined in such rats in vivo, e.g. as described in Example 7.
  • the compounds of the invention inhibits in vivo food intake in non-obese Sprague Dawley rats.
  • Diet-Induced Obese (DIO) Sprague Dawley rats is another example of a suitable animal model, and the changes in food intake may be determined in such rats in vivo,
  • the compounds of the invention inhibits in vivo food intake and lowers body weight in DIO Sprague Dawley rats.
  • MIC-1 compounds of the present invention may be produced by means of recombinant protein technology known to persons skilled in the art.
  • nucleic acid sequences encoding the proteins of interest or functional variants thereof are modified to encode the desired MIC-1 compound. This modified sequence is then inserted into an expression vector, which is in turn transformed or transfected into the expression host cells.
  • the nucleic acid construct encoding the MIC-1 compound may suitably be of genomic, cDNA or synthetic origin. Amino acid sequence alterations are accomplished by modification of the genetic code by well-known techniques.
  • the DNA sequence encoding the MIC-1 compound is usually inserted into a recombinant vector which may be any vector, which may conveniently be subjected to recombinant DNA procedures, and the choice of vector will often depend on the host cell into which it is to be introduced.
  • the vector may be an autonomously replicating vector, i.e. a vector, which exists as an extrachromosomal entity, the replication of which is independent of chromosomal replication, e.g. a plasmid.
  • the vector may be one which, when introduced into a host cell, is integrated into the host cell genome and replicated together with the chromosome(s) into which it has been integrated.
  • the vector is preferably an expression vector in which the DNA sequence encoding the MIC-1 compound is operably linked to additional segments required for transcription of the DNA.
  • operably linked indicates that the segments are arranged so that they function in concert for their intended purposes, e.g. transcription initiates in a promoter and proceeds through the DNA sequence coding for the polypeptide until it terminates within a terminator.
  • expression vectors for use in expressing the MIC-1 compound will comprise a promoter capable of initiating and directing the transcription of a cloned gene or cDNA.
  • the promoter may be any DNA sequence, which shows transcriptional activity in the host cell of choice and may be derived from genes encoding proteins either homologous or heterologous to the host cell.
  • expression vectors for expression of the MIC-1 compound will also comprise a terminator sequence, a sequence recognized by a host cell to terminate transcription.
  • the terminator sequence is operably linked to the 3′ terminus of the nucleic acid sequence encoding the polypeptide. Any terminator which is functional in the host cell of choice may be used in the present invention.
  • Expression of the MIC-1 compound can be aimed for either intracellular expression in the cytosol of the host cell or be directed into the secretory pathway for extracellular expression into the growth medium.
  • Intracellular expression is the default pathway and requires an expression vector with a DNA sequence comprising a promoter followed by the DNA sequence encoding the MIC-1 compound followed by a terminator.
  • a secretory signal sequence (also known as signal peptide or a pre sequence) is needed as an extension of the MIC-1 sequence.
  • a DNA sequence encoding the signal peptide is joined to the 5′ end of the DNA sequence encoding the MIC-1 compound in the correct reading frame.
  • the signal peptide may be that normally associated with the protein or may be from a gene encoding another secreted protein.
  • the host cell into which the DNA sequence encoding the MIC-1 compound is introduced may be any cell that is capable of expressing the MIC-1 compound either intracellularly or extracellularly.
  • the MIC-1 compound may be produced by culturing a host cell containing a DNA sequence encoding the MIC-1 compound and capable of expressing the MIC-1 compound in a suitable nutrient medium under conditions permitting the expression of the MIC-1 compound.
  • host cells suitable for expression of MIC-1 compounds are: Escherichia coli, Saccharomyces cerevisiae, as well as human embryonic kidney (HEK), Baby Hamster Kidney (BHK) or Chinese hamster ovary (CHO) cell lines. If posttranslational modifications are needed, suitable host cells include yeast, fungi, insects and higher eukaryotic cells such as mammalian cells.
  • MIC-1 compound Once the MIC-1 compound has been expressed in a host organism it may be recovered and purified to the required quality by conventional techniques.
  • Non-limiting examples of such conventional recovery and purification techniques are centrifugation, solubilization, filtration, precipitation, ion-exchange chromatography, immobilized metal affinity chromatography (IMAC), Reversed phase—High Performance Liquid Chromatography (RP-HPLC), gel-filtration and freeze drying.
  • MIC-1 proteins examples include Chich et al, Anal. Biochem, 1995, 224, pp 245-249 and Xin et al., Protein Expr. Purif. 2002, 24, pp530-538.
  • MIC-1 compounds can be expressed in bacteria such as E. coli.
  • large scale protein production of said MIC-1 polypeptides with an N-extension could take of using Inclusion Bodies (IB) as this represent an advantageous approach to controlling process recovery, protein purity, protease degradation and general protein stability. This becomes particular important for large scale protein production.
  • IB Inclusion Bodies
  • the balance of MIC-1 polypeptides with an N-extension solubility partly controlled by the calculated pI and IB formation.
  • treatment is meant to include both the prevention and minimization of the referenced disease, disorder, or condition (i.e., “treatment” refers to both prophylactic and therapeutic administration of a compound of the invention or composition comprising a compound of the invention unless otherwise indicated or clearly contradicted by context.
  • the route of administration may be any route which effectively transports a compound of this invention to the desired or appropriate place in the body, such as parenterally, for example, subcutaneously, intramuscularly or intraveneously.
  • a compound of this invention can be administered orally, pulmonary, rectally, transdermally, buccally, sublingually, or nasally.
  • the amount of a compound of this invention to be administered is decided in consultation with a practitioner who is familiar with the treatment of obesity and related disorders.
  • compositions comprising a compound of the invention or a pharmaceutically acceptable salt, amide, or ester thereof, and a pharmaceutically acceptable excipient may be prepared as is known in the art.
  • excipient broadly refers to any component other than the active therapeutic ingredient(s).
  • the excipient may be an inert substance, an inactive substance, and/or a not medicinally active substance.
  • the excipient may serve various purposes, e.g. as a carrier, vehicle, diluent, tablet aid, and/or to improve administration, and/or absorption of the active substance.
  • the treatment with a compound according to the present invention may also be combined with one or more pharmacologically active substances, e.g., selected from antiobesity agents, appetite regulating agents, and agents for the treatment and/or prevention of complications and disorders resulting from or associated with obesity.
  • one or more pharmacologically active substances e.g., selected from antiobesity agents, appetite regulating agents, and agents for the treatment and/or prevention of complications and disorders resulting from or associated with obesity.
  • the present invention relates to a compound of the invention, for use as a medicament.
  • the compound of the invention may be used for the following medical treatments:
  • the invention relates to a method for weight management. In some embodiments the invention relates to a method for reduction of appetite. In some embodiments the invention relates to a method for reduction of food intake.
  • the invention relates to a method for treatment or prevention of obesity. In some embodiments the invention relates to use of the MIC-1 compounds of the invention for treatment or prevention of obesity.
  • the subject suffering from obesity is human, such as an adult human or a paediatric human (including infants, children, and adolescents).
  • a human subject suffering from obesity may have a BMI of ⁇ 30; this subject may also be referred to as obese.
  • the human subject suffering from obesity may have a BMI of ⁇ 35 or a BMI in the range of ⁇ 30 to ⁇ 40.
  • the obesity is severe obesity or morbid obesity, wherein the human subject may have a BMI of ⁇ 40.
  • the invention relates to a method for treatment or prevention of overweight, optionally in the presence of at least one weight-related comorbidity. In some embodiments the invention relates to use of the MIC-1 compounds of the invention for treatment or prevention of overweight, optionally in the presence of at least one weight-related comorbidity.
  • the subject suffering from overweight is human, such as an adult human or a paediatric human (including infants, children, and adolescents).
  • a human subject suffering from overweight may have a BMI of such as a BMI of
  • a human subject suffering from overweight has a BMI in the range of 25 to ⁇ 30 or in the range of 27 to ⁇ 30.
  • the weight-related comorbidity is selected from the group consisting of hypertension, diabetes (such as type 2 diabetes), dyslipidaemia, high cholesterol, and obstructive sleep apnoea.
  • the invention relates to a method for reduction of body weight. In some embodiments the invention relates to use of the MIC-1 compounds of the invention for reduction of body weight.
  • a human to be subjected to reduction of body weight according to the present invention may have a BMI of ⁇ 25, such as a BMI of ⁇ 27 or a BMI of ⁇ 30. In some embodiments the human to be subjected to reduction of body weight according to the present invention may have a BMI of ⁇ 35 or a BMI of ⁇ 40.
  • the term “reduction of body weight” may include treatment or prevention of obesity and/or overweight.
  • the invention relates to a method for treatment or prevention of cardiovascular diseases like arteriosclerosis and other disorders such as steatohepatitis, and diabetic nephropathy.
  • a MIC-1 polypeptide means one MIC-1 polypeptide or more than one MIC-1 polypeptide.
  • Main peak refers to the peak in a purification chromatogram which has the highest UV intensity in milliabsorbance units and which contains the fusion protein.
  • HPLC High performance liquid chromatography
  • SDS-PAGE is Sodium dodecyl sulfate Polyacrylamide gel electrophoresis.
  • IMAC is immobilized metal affinity chromatography.
  • SEC is size exclusion chromatography
  • MS is mass spectrometry.
  • MIC-1 compounds were designed to have increased solubility. In an aspect of the invention, this was achieved by adding an N-terminal “acidic” extension to the MIC-1 polypeptide. In an aspect of the invention, solubility were enhanced and stability improved by modification of the amino acid sequence of the MIC-1 polypeptide. For example extensions were added to the N terminal of a MIC-1 polypeptide, and/or modification was done within the amino acid sequence of the MIC-1 polypeptide (in-sequence mutation).
  • N-terminal amino acid_extension F, I, L, M, V, W and Y were excluded, since they could contribute to protein aggregation. H, K, and R were also excluded, since they could cause undesired binding on cell membrane.
  • A, E, G, P, S, T, D, N, and Q are preferred for the N-extension sequence. E and D are particularly preferred since they increase the solubility by decreasing pI value of the compound.
  • one or two additional Alanine(s) were added at the very N-terminal to increase the initial Methionine removing efficiency when MIC-1 compounds were expressed in E.coli.
  • N-terminal amino acid_extensions were designed based on the above principles. Some N-extensions comprise sequences originating from human proteins (humanized sequences); some comprise artificially designed sequence(s) (e.g. GS, SG, AEE, AES, GEPQ (SEQ ID NO:123), GEPS (SEQ ID NO:118)); some comprise several repeats of the humanized sequences or artificial sequences; some comprise a combination of the above. Several 6-residue sequences (6-mers) were designed. N-extensions could comprise one or more of a 6-mers, part of a 6-mers (e.g., 1-5 residues of a 6-mers), or a combination of the above. The amino acid residues of the artificial sequences (including 6-mers) and the humanized sequences could be arranged in any order.
  • 6-mer-1 SPAGSP (SEQ ID NO: 4)
  • 6-mer-2 TSESAT (SEQ ID NO: 5)
  • 6-mer-3 TSTEPE (SEQ ID NO: 6)
  • 6-mer-4 SEPATS (SEQ ID NO: 7)
  • 6-mer-5 TSTEEG (SEQ ID NO: 8)
  • 6-mer-6 PESGPG (SEQ ID NO: 9)
  • 6-mer-7 SGSAPG (SEQ ID NO: 10)
  • GSETPG SEQ ID NO: 11)
  • N-extensions Residue SEQ ID NO number Sequence of N-extension SEQ ID NO: 54 6 AEEAES SEQ ID NO: 55 3 AES SEQ ID NO: 56 9 (AEE) 2 AES SEQ ID NO: 57 20 (GEPS) 5 SEQ ID NO: 58 24 SPAGSPTSTEEGTSESATPESGPG SEQ ID NO: 59 21 (AEE) 6 AES SEQ ID NO: 60 18 (AEE) 5 AES SEQ ID NO: 61 12 (AEE) 3 AES SEQ ID NO: 62 26 AASPAGSPTSTEEGTSESATPESGPG SEQ ID NO: 63 24 TSESATPESGPGTSESATPESGPG SEQ ID NO: 64 26 AASPAGSPTSTEEGTSESATPESGPG SEQ ID NO: 65 22 AAPEDEETPEQEGSGSGSGSGSGS SEQ ID NO: 66 12 AAPEDEETPEQE SEQ ID NO: 67 22 AAPDEGTEEETEGSGSGSGSGSGS SEQ ID NO:
  • Certain internal residues of MIC-1 were modified, e.g. by substitution.
  • a hydrophobic residue of MIC-1 could be substituted with a hydrophilic residue, preferably by with an acidic residue; a positive charged residue could be substituted with an acidic residue, etc.
  • methionine could be substituted with other amino acids, e.g. E, F or L.
  • In-sequence mutations for increasing solubility include but are not limited to: P11E, H18E, R21E, A30E, A47E, R53E, A54E, M57E, R67E, L68E, K69E, A75E, A81E, P85E, L105E and K107E.
  • In-sequence mutations for decreasing oxidation include but are not limited to: M43L, M57E, M57L, M86F and M86L.
  • In-sequence mutations for increasing chemical stability include but are not limited to R2S, R2A, N3S N3E, N3A, N3T, N3P, N3G, N3V, N3H, N3Y and N3Q.
  • the calculated pI of a MIC-1 compound is defined as the pH at which the net calculated charge of the compound is zero.
  • the calculated charge of the MIC-1 compound as a function of pH is obtained using the pKa values of the amino acid residues described in Table 1 and the method described by B. Skoog and A. Wichman (Trends in Analytical Chemistry, 1986, vol. 5, pp. 82-83).
  • the side chain pKa of cysteine (Cys) is only included in the charge calculation for cysteines with a free sulfhydryl group.
  • the calculated pI value of human wtMIC-1 is 8.8 as the homodimer.
  • Example-1 Expression and Fermentation of the MIC-1 Compounds
  • the cDNA of MIC-1 compound was sub-cloned into a pET11b derived vector.
  • Overexpression of MIC-1 compounds as inclusion bodies was induced in E. coli by 0.5 mM isopropyl ⁇ -d-thiogalactoside (IPTG) when the cell density reached an OD600 of 1.0.
  • IPTG isopropyl ⁇ -d-thiogalactoside
  • Fermentation was carried out on fed-batch process in chemical defined medium as supplement. Fermentation yield largely depended on different compounds, which varied from 1 g/L to 8 g/L from compound to compound.
  • Example-2 Purification and Refolding:
  • the MIC-1 compounds were further purified as follows:
  • the resulting solution was filtered by 0.4 ⁇ m filter and loaded onto Hydrophobic Interaction column or anion exchange chromatography (50 mM Tris pH 8.0, 0-500 mM NaCl) using Q Sepharose Fast Flow resin (GE Healthcare), as generally described in Protein Purification. Principles and Practice Series: Springer Advanced Texts in Chemistry Scopes, Robert K. 3rd ed., 1994 (Chapter 6 and Chapter 8).
  • further purification was done by size exclusion chromatography using a HiLoad 26/60 Superdex pg 75 column (GE Healthcare) operated with 50 mM Tris pH 8.0 and 200 mM NaCl.
  • the MIC-1 compounds was transferred to DPBS, and stored frozen.
  • SEQ ID NO: 82 MIC-1(R2A, N3E, M57E) 6.4 1.7 SEQ ID NO: 83 MIC-1(R2A, N3E, P85E) 6.4 N.D.
  • SEQ ID NO: 84 MIC-1(R2A, N3E, P11E) 6.4 1.6 SEQ ID NO: 85 MIC-1(R2A, N3E, R21E) 6.1 1.8
  • SEQ ID NO: 90 AES-MIC-1- ⁇ 1-3 6.8 0.9 SEQ ID NO: 91 (AEE) 2 AES-MIC-1- ⁇ 1-3 5.5 N.D.
  • SEQ ID NO: 92 GEPS 5 -MIC-1(SEQ ID NO: 1) 5.8 35.1
  • SEQ ID NO: 93 SPAGSPTSTEEGTSESATPESGPG- 6.1 44.5
  • MIC-1(SEQ ID NO: 1) SEQ ID NO: 94 (AEE) 6 AES-MIC-1(SEQ ID NO: 1) 4.5 39.0 SEQ ID NO: 95 (AEE) 5 AES-MIC-1- ⁇ 1-3 4.6 35.0 SEQ ID NO: 96 (AEE) 3 AES-MIC-1- ⁇ 1-3 5.0 36.0
  • PG-MIC-1(SEQ ID NO: 1) SEQ ID NO: 98 TSESATPESGPGTSESATPESGPG- 5.5 N.D.
  • MIC-1(R2A, N3E) SEQ ID NO: 99 AASPAGSPTSTEEGTSESATPESG 5.8 N.D.
  • PG-MIC-1- ⁇ 1-3 SEQ ID NO: 100 AAPEDEETPEQEGSGSGSGS- 5.2 35.7 MIC-1- ⁇ 1-3 SEQ ID NO: 101 AAPEDEETPEQE-MIC-1- ⁇ 1-3 5.2 N.D.
  • SEQ ID NO: 102 AAPDEGTEEETEGSGSGSGSGS- 5.2 N.D.
  • SEQ ID NO: 116 GEPS 6 -MIC-1- ⁇ -3 5.2 N.D.
  • SEQ ID NO: 117 SEPATSGSETPG 2 -MIC-1-des- 6.1 N.D. N3 *N.D.: Not determined
  • Example-3 pH-Dependent Solubility of MIC-1 Compounds of the Invention
  • MIC-1 compounds were dissolved in a mixture of water and ethanol (60% water and 40% ethanol) with a concentration range between 3 mg/ml to 10 mg/ml. The solvent was evaporated with SpeedVac (Concentrator Plus, Eppendorf) for 6 hours to obtain pellet of said MIC-1 compound.
  • Buffers were added into each well of the 96-well plate together with MIC-1 compounds.
  • the amount used may not be exactly the same but all targeting a theoretical concentration within 12-18 mg/ml.
  • the concentration of MIC-1 compounds in the supernatant was determined by UPLC (Table 6). Based on the results, solubility of the MIC-1 compounds of the invention was significantly improved between pH 6-9 compared with wtMIC-1.
  • the optimal pH window of the MIC-1 compounds falls into the pH range that is preferred for formulation, e.g. pH 6.5-8.5.
  • the MIC-1 compounds were dissolved in a mixture of water and ethanol (60% water and 40% ethanol) with a concentration range between 3 mg/ml to 10 mg/ml. Then the solution (150 ⁇ L each well) was aliquot into a 96-well plate (Corning). The solvent was evaporated with SpeedVac (Concentrator Plus, Eppendorf) for 6 hours to obtain pellet of the MIC-1 compound. Tris buffer (pH 8.0, without excipients) was added into each well of the 96-well plate. The amount of buffer added to the well was less than the amount needed for solving the whole pellet in the well, so that maximal concentration was achieved.
  • the plate was shaken on a plate shaker at 800 rpm (MixMate, Eppendorf) for 2 hours. The pellet was spun down at 3600 g for 5 min. The supernatants were transferred to a 96-deep-well plate and diluted 20 times with 40% ethanol. Then all of the samples were subject to UPLC (Acquity, Waters), plate reader (Infinite M200 pro, Tecan) and UV spectrometer (NanoDrop 8000, Thermo Scientific) to determine the concentration (Table 7)
  • solubility of the MIC-1 compounds of the invention was significantly improved at pH 8.0.
  • the MIC-1 compounds with N-extensions achieved solubility of more than 30 mg/ml at pH 8.0.
  • the purpose of this example was to establish a cell based in vitro assay for testing MIC-1 activity.
  • Mammalian cells were transfected and stably expressed full length MIC-1 receptor (hGFRAL) and its full signaling co-receptor hRET51.
  • Plasmids expressing full length hGFRAL and full length hRET51 were constructed by inserting synthesized DNA nucleotides encoding full length hGFRAL and full length hRET51 into mammalian expression vector pEL.
  • IRES internal ribosome entry site
  • pEL vector backbone was provided by Taihegene CRO company.
  • Example 6 MIC-1 Cell-Based in Vitro Activity Assay
  • Results from screening MIC-1 compounds using BHK21-hGFRAL-IRES-hRET is shown in Table 8.
  • HSA Human Serum Albumin
  • HSA-MIC-1 conjugates pERK Calcu- EC50 lated HSA-MIC-1 fusion protein (nM) pI HSA-GGSSSGS(SEQ ID NO: 152)-MIC-1 3.6 6.2 (SEQ ID NO: 1) HSA-PTPTPTPTPTPTPTPTPTPTPTPTPTPTPTPTPTPTPTPTPTPTPTPTPTPTPTPTPTPTPTPTPTPTPTPTPTPTPTPTPTPTPTPTPTPTP 4.5 6.2 (SEQ ID NO: 153)-MIC-1(SEQ ID NO: 1)
  • mice were acclimatized for at least 7 days prior to the experiment. Collected data are expressed as daily food intake (24 hour food intake) measured from the onset of each daily 12 hour dark phase to the next day dark phase. Daily changes in food intake in response to administrated compound were calculated by subtracting the average daily food intake of the vehicle group from the average daily food intake of the treatment group. Changes were considered significant if p ⁇ 0.1 using a two-tailed student's t-test ( ). Results are expressed as the “maximum reduction” in food intake compared with vehicle (percentage) recorded during the study period. Data are also expressed as the “accumulated reduction” in food intake which as the sum of significant (p ⁇ 0.1) daily reductions in food intake (percentage) during the study period.
  • N-Formyl-Methionine is recognized by the immune system as foreign material, or as an alarm signal released by damaged cells, and stimulates the body to fight against potential infection (Pathologic Basis of Veterinary Disease5: Pathologic Basis of Veterinary Disease, By James F. Zachary, M. Donald McGavin).
  • Methionine is an instable residue that could be easily oxidized. Therefore, the N-Met cleavage efficiency is very important to MIC-1 expression.
  • the cDNA of MIC-1 compound was sub-cloned into a pET11b derived vector.
  • Overexpression of MIC-1 compounds as inclusion bodies or soluble protein was induced in E. coli by 0.5mM isopropyl ⁇ -d-thiogalactoside (IPTG) when the cell density reached an OD600 of 1.0.
  • IPTG isopropyl ⁇ -d-thiogalactoside
  • Fermentation was carried out on fed-batch process in chemical defined medium as supplement. Fermentation yield largely depended on different compounds, which varied from 1 g/L to 8 g/L from compound to compound.
  • N-extensions starting with the 12mer-1 block could not be expressed in E. coli.
  • protein expression was achieved but only 12mer-4 as the initial sequence resulted in complete methionine cleavage.
  • the N-met cleavage efficiency of 12mer-2 series is better than that of 12mer-3 series.
  • Example 9 Expression Level and Inclusion Body Ratio of MIC-1 Peptide Compound with 2* or 2.5*12mer N-Extension
  • Example 8 for protein production method. The results are shown in Table 13, FIG. 3 and FIG. 4 .
  • inclusion body is usually considered as a good choice mainly due to its better up-scaling properties, which mainly include: high expression level, simple recovery step and high purity, protease-resistant and good process stability.
  • MIC-1 compounds could be expressed either inclusion body or soluble form, which is mainly dependent on compounds' pI and extension length. The results are shown in Table 14 and FIG. 4 .
  • MIC-1 compounds initiating with 12mer-(4+2+_), -(4+4+_) and -(4+3+_) were investigated with their ability to express inclusion body. It was shown that the inclusion body ratio is >90% when pI>5.1.
  • MIC-1 compounds with in-sequence mutations M57E/H66E mainly expressed soluble fractions.

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Organic Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Molecular Biology (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Biochemistry (AREA)
  • Biophysics (AREA)
  • Genetics & Genomics (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Zoology (AREA)
  • Epidemiology (AREA)
  • Immunology (AREA)
  • Toxicology (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Endocrinology (AREA)
  • Child & Adolescent Psychology (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Peptides Or Proteins (AREA)
US16/303,516 2016-05-24 2017-05-24 MIC-1 Compounds and Use Thereof Abandoned US20190248852A1 (en)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
CN2016083104 2016-05-24
CNPCT/CN2016/083104 2016-05-24
CN2016103574 2016-10-27
CNPCT/CN2016/103574 2016-10-27
PCT/EP2017/062583 WO2017202936A1 (en) 2016-05-24 2017-05-24 Mic-1 compounds and use thereof

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2017/062583 A-371-Of-International WO2017202936A1 (en) 2016-05-24 2017-05-24 Mic-1 compounds and use thereof

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US17/194,908 Continuation US20210198331A1 (en) 2016-05-24 2021-03-08 Mic-1 compounds and use thereof

Publications (1)

Publication Number Publication Date
US20190248852A1 true US20190248852A1 (en) 2019-08-15

Family

ID=59009675

Family Applications (3)

Application Number Title Priority Date Filing Date
US16/303,516 Abandoned US20190248852A1 (en) 2016-05-24 2017-05-24 MIC-1 Compounds and Use Thereof
US17/194,908 Abandoned US20210198331A1 (en) 2016-05-24 2021-03-08 Mic-1 compounds and use thereof
US18/083,811 Active US12006344B2 (en) 2016-05-24 2022-12-19 MIC-1 compounds and use thereof

Family Applications After (2)

Application Number Title Priority Date Filing Date
US17/194,908 Abandoned US20210198331A1 (en) 2016-05-24 2021-03-08 Mic-1 compounds and use thereof
US18/083,811 Active US12006344B2 (en) 2016-05-24 2022-12-19 MIC-1 compounds and use thereof

Country Status (18)

Country Link
US (3) US20190248852A1 (es)
EP (1) EP3463412A1 (es)
JP (1) JP7013390B2 (es)
KR (1) KR102433503B1 (es)
CN (1) CN109414471A (es)
AU (1) AU2017269496B2 (es)
BR (1) BR112018072034A2 (es)
CA (1) CA3025251A1 (es)
CL (1) CL2018003319A1 (es)
CO (1) CO2018012258A2 (es)
IL (1) IL262926A (es)
MA (1) MA45113A (es)
MX (1) MX2018014023A (es)
PE (1) PE20190117A1 (es)
PH (1) PH12018502465A1 (es)
SA (1) SA518400460B1 (es)
TW (1) TW201741333A (es)
WO (1) WO2017202936A1 (es)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10752664B2 (en) 2011-04-08 2020-08-25 Amgen Inc. Method of treating or ameliorating metabolic disorders using growth differentiation factor 15 (GDF-15)
US10894814B2 (en) 2013-07-31 2021-01-19 Amgen Inc. Growth differentiation factor 15 (GDF-15) constructs
US11161889B2 (en) 2018-04-09 2021-11-02 Amgen Inc. Growth differentiation factor 15 fusion proteins
US12006344B2 (en) 2016-05-24 2024-06-11 Novo Nordisk A/S MIC-1 compounds and use thereof
US12544427B2 (en) 2020-10-02 2026-02-10 Amgen Inc. Use of GDF15 for treating cardiometabolic syndrome and other conditions

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI759301B (zh) 2016-05-24 2022-04-01 美商安美基公司 聚乙二醇化卡非佐米化合物
JP7134960B2 (ja) 2016-12-06 2022-09-12 セントビンセンツ ホスピタル シドニー リミテッド 肥満及び摂食障害の治療
TWI710377B (zh) * 2017-05-23 2020-11-21 丹麥商諾佛 儂迪克股份有限公司 Ｍｉｃ－１化合物及其用途
WO2020031149A2 (en) 2018-08-10 2020-02-13 Novartis Ag Gfral extracellular domains and methods of use
JP7539902B2 (ja) 2018-10-22 2024-08-26 ヤンセン・サイエンシズ・アイルランド・アンリミテッド・カンパニー グルカゴン様ペプチド１（ｇｌｐ１）－増殖分化因子１５（ｇｄｆ１５）融合タンパク質及びその使用
WO2021067655A1 (en) 2019-10-04 2021-04-08 Amgen Inc. Use of gdf15 for treating cardiometabolic syndrome and other conditions
WO2021136223A1 (en) 2019-12-31 2021-07-08 Beijing Ql Biopharmaceutical Co., Ltd. Fusion proteins of glp-1 and gdf15 and conjugates thereof
WO2022089435A1 (en) * 2020-10-27 2022-05-05 Beijing Ql Biopharmaceutical Co., Ltd. Fusion proteins of gdf15 and use thereof

Family Cites Families (38)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ZA954983B (en) * 1994-06-17 1996-02-14 Novo Nordisk As N-terminally extended proteins expressed in yeast
AU3247699A (en) 1998-02-17 1999-09-06 Novo Nordisk A/S Lipase variant
WO2001077137A1 (en) 2000-04-12 2001-10-18 Human Genome Sciences, Inc. Albumin fusion proteins
CN1152942C (zh) 2000-05-30 2004-06-09 华东理工大学 含载流子传输功能团的分子扭曲型电致发光材料及其应用
CA2390820A1 (en) * 2002-06-17 2003-12-17 St. Vincent's Hospital Sydney Limited Methods of diagnosis, prognosis and treatment of cardiovascular disease
CN1241946C (zh) 2002-07-01 2006-02-15 美国福源集团 对多种细胞具刺激增生作用的人血清白蛋白重组融合蛋白
DK2441466T3 (da) 2004-04-13 2014-10-27 St Vincents Hosp Sydney MIC-1-inhiberende middel
DK1751184T3 (da) 2004-05-13 2009-11-23 Lilly Co Eli FGF-21 fusionsproteiner
EP1771467A2 (en) 2004-07-26 2007-04-11 Asterion Limited Linkers
ES2531372T3 (es) 2006-10-13 2015-03-13 Novo Nordisk Healthcare Ag Enzimas de procesamiento fusionadas a marcadores de proteínas básicas
CN103298935A (zh) 2007-08-15 2013-09-11 阿穆尼克斯公司 用于改善生物活性多肽性能的组合物和方法
RU2525393C2 (ru) 2009-01-23 2014-08-10 Ново Нордиск А/С Производные fgf21 со связующим альбумина а-в-с-d-e- и их применение
US8680050B2 (en) * 2009-02-03 2014-03-25 Amunix Operating Inc. Growth hormone polypeptides fused to extended recombinant polypeptides and methods of making and using same
EA020843B1 (ru) 2009-02-03 2015-02-27 Амуникс Оперейтинг Инк. Удлиненные рекомбинантные полипептиды и содержащие их композиции
ES2705249T3 (es) 2009-06-08 2019-03-22 Amunix Operating Inc Polipéptidos reguladores de glucosa y métodos para su producción y uso
ES2993140T3 (en) 2010-04-02 2024-12-23 Amunix Pharmaceuticals Inc Binding fusion proteins, binding fusion protein-drug conjugates, xten-drug conjugates and methods of making and using same
US10752664B2 (en) 2011-04-08 2020-08-25 Amgen Inc. Method of treating or ameliorating metabolic disorders using growth differentiation factor 15 (GDF-15)
BR112014018575A2 (pt) 2012-01-26 2017-07-04 Amgen Inc polipetídeos de fator de diferenciação de crescimento 15 (gdf-15)
US9550819B2 (en) * 2012-03-27 2017-01-24 Ngm Biopharmaceuticals, Inc. Compositions and methods of use for treating metabolic disorders
CA2899170C (en) 2013-01-30 2022-08-02 Ngm Biopharmaceuticals, Inc. Compositions and methods of use in treating metabolic disorders
US9161966B2 (en) 2013-01-30 2015-10-20 Ngm Biopharmaceuticals, Inc. GDF15 mutein polypeptides
MX369152B (es) 2013-07-31 2019-10-30 Amgen Inc Construcciones del factor de diferenciación de crecimiento 15 (gdf-15).
EP3036262A4 (en) 2013-08-22 2017-03-01 Acceleron Pharma Inc. Tgf-beta receptor type ii variants and uses thereof
US10588980B2 (en) 2014-06-23 2020-03-17 Novartis Ag Fatty acids and their use in conjugation to biomolecules
RU2017101436A (ru) * 2014-06-24 2018-07-24 Ново Нордиск А/С Mic-1 слитные белки и их применение
SG11201700378PA (en) 2014-07-30 2017-02-27 Ngm Biopharmaceuticals Inc Compositions and methods of use for treating metabolic disorders
AU2015339134B2 (en) * 2014-10-30 2021-06-17 Acceleron Pharma Inc. Methods and compositions using GDF15 polypeptides for increasing red blood cells
DK3212226T3 (da) 2014-10-31 2020-06-15 Ngm Biopharmaceuticals Inc Sammensætninger og anvendelsesfremgangsmåder til behandling af metaboliske lidelser
DK3236991T3 (da) 2014-12-23 2019-08-26 Novo Nordisk As Fgf21-derivater og anvendelser deraf
MA41794A (fr) 2015-03-18 2018-01-23 The California Institute For Biomedical Res Agents thérapeutiques modifiés et compositions associées
US20170008928A1 (en) 2015-07-06 2017-01-12 Novo Nordisk A/S Novel peptides and peptide derivatives and uses thereof
EA201890850A1 (ru) 2015-10-02 2018-09-28 Юлиус-Максимилианс-Универзитет Вюрцбург Комбинированное лечение с использованием ингибиторов человеческого фактора роста и дифференцировки 15 (gdf-15) и блокаторов контрольных точек иммунного ответа
ES2968226T3 (es) 2015-10-02 2024-05-08 Univ Wuerzburg J Maximilians GDF-15 como marcador de diagnóstico para predecir la evolución clínica de un tratamiento con bloqueadores de puntos de control inmunitario
GB201517528D0 (en) 2015-10-02 2015-11-18 Julius Maximillians Universitãt Würzburg GDF-15 as a diagnosis marker for melanoma
WO2017109706A1 (en) 2015-12-22 2017-06-29 Novartis Ag Methods of treating or ameliorating metabolic disorders using growth differentiation factor 15 (gdf-15)
US10336812B2 (en) 2016-05-10 2019-07-02 Janssen Biotech, Inc. GDF15 fusion proteins and uses thereof
TW201741333A (zh) 2016-05-24 2017-12-01 諾佛 儂迪克股份有限公司 Ｍｉｃ－１化合物及其用途
TWI710377B (zh) 2017-05-23 2020-11-21 丹麥商諾佛 儂迪克股份有限公司 Ｍｉｃ－１化合物及其用途

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10752664B2 (en) 2011-04-08 2020-08-25 Amgen Inc. Method of treating or ameliorating metabolic disorders using growth differentiation factor 15 (GDF-15)
US10894814B2 (en) 2013-07-31 2021-01-19 Amgen Inc. Growth differentiation factor 15 (GDF-15) constructs
US12006344B2 (en) 2016-05-24 2024-06-11 Novo Nordisk A/S MIC-1 compounds and use thereof
US11161889B2 (en) 2018-04-09 2021-11-02 Amgen Inc. Growth differentiation factor 15 fusion proteins
US12054527B2 (en) 2018-04-09 2024-08-06 Amgen Inc. Growth differentiation factor 15 fusion proteins
US12544427B2 (en) 2020-10-02 2026-02-10 Amgen Inc. Use of GDF15 for treating cardiometabolic syndrome and other conditions

Also Published As

Publication number Publication date
IL262926A (en) 2018-12-31
RU2018141829A (ru) 2020-06-25
SA518400460B1 (ar) 2022-09-21
KR102433503B1 (ko) 2022-08-18
CO2018012258A2 (es) 2018-11-30
PH12018502465A1 (en) 2019-04-08
CL2018003319A1 (es) 2019-02-01
TW201741333A (zh) 2017-12-01
AU2017269496A1 (en) 2018-11-15
US12006344B2 (en) 2024-06-11
JP7013390B2 (ja) 2022-01-31
RU2018141829A3 (es) 2020-10-07
PE20190117A1 (es) 2019-01-16
EP3463412A1 (en) 2019-04-10
AU2017269496B2 (en) 2021-03-25
JP2019520333A (ja) 2019-07-18
WO2017202936A1 (en) 2017-11-30
KR20190008290A (ko) 2019-01-23
MX2018014023A (es) 2019-04-04
US20230212245A1 (en) 2023-07-06
MA45113A (fr) 2019-04-10
CN109414471A (zh) 2019-03-01
US20210198331A1 (en) 2021-07-01
BR112018072034A2 (pt) 2019-02-12
CA3025251A1 (en) 2017-11-30

Similar Documents

Publication Publication Date Title
US12006344B2 (en) MIC-1 compounds and use thereof
US9956264B2 (en) MIC-1 fusion proteins and uses thereof
KR101573636B1 (ko) 신규한 옥신토모듈린 유도체 및 이를 포함하는 비만 치료용 조성물
JP6058646B2 (ja) 多置換インスリン
US20230364248A1 (en) Mic-1 compounds and uses thereof
CN113396157A (zh) 具有降低的胰岛素受体结合亲和力的胰岛素类似物
KR20170134542A (ko) 프로톡신-ii 변이체 및 사용 방법
US20170334971A1 (en) Alpha-1-Antitrypsin (A1AT) Fusion Proteins and Uses Thereof
RU2776529C2 (ru) Соединения mic-1 и их применение

Legal Events

Date Code Title Description
AS Assignment

Owner name: NOVO NORDISK A/S, DENMARK

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:ZHANG, XUJIA;GAO, XIANG;GUAN, HONGTAO;AND OTHERS;SIGNING DATES FROM 20181001 TO 20190319;REEL/FRAME:048806/0242

STPP Information on status: patent application and granting procedure in general

Free format text: DOCKETED NEW CASE - READY FOR EXAMINATION

STPP Information on status: patent application and granting procedure in general

Free format text: NON FINAL ACTION MAILED

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION