CN1493591A - Polypeptide-human protein synthetic protein L14, 22 and nucleotide for coding said polypeptide - Google Patents
Polypeptide-human protein synthetic protein L14, 22 and nucleotide for coding said polypeptide Download PDFInfo
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- CN1493591A CN1493591A CNA021377278A CN02137727A CN1493591A CN 1493591 A CN1493591 A CN 1493591A CN A021377278 A CNA021377278 A CN A021377278A CN 02137727 A CN02137727 A CN 02137727A CN 1493591 A CN1493591 A CN 1493591A
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- polypeptide
- polynucleotide
- sequence
- protein
- human protein
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Abstract
A novel polypeptide-human protein synthesizing protein L14.22, the polynucleotide for coding it, the process for preparing said polypeptide by DNA recombination, the application of said polypeptide in treating diseases, such as cancer, HIV infection, immunopathy, etc. the antagonist of said polypeptide and its medical action, and the application of said polynucleotide are disclosed.
Description
Technical field
The invention belongs to biological technical field, specifically, the invention describes a kind of polypeptide-human protein synthetic protein L14.22, and the polynucleotide sequence of this polypeptide of encoding.The invention still further relates to the preparation method and the application of these polynucleotide and polypeptide.
Background technology
Rrna is the organoid of synthetic protein, and main component is protein and ribosome-RNA(rRNA).Ribosomal protein is very conservative, plays an important role in ribosomal translation process, and for example: the three-dimensional structure that rRNA is folded into function plays an important role; In protein synthesis, a series of variation takes place in ribosomal space conformation, and some ribosomal protein may play " fine setting " effect to ribosomal conformation; On ribosomal binding site even may be in katalysis, the common functionating of ribosomal protein and rRNA.Other researchs find that also some ribosomal protein still is the cell proliferation and the regulation of apoptosis factor.[Fannie?W.Chen?et?al，International?Reviews?of?Immunology?1998]
L14 albumen is the most conservative a kind of ribosomal protein, plays an important role in rrna nucleic acid-albumen composition.Studies show that in large ribosomal subunit L14 albumen is in occupation of the central position of peptidy transeferace and GTP enzyme.L14 albumen contains one by 5 strands of barrel-like structures of forming, and the C-terminal ring texture comprises two little spirane structures, also comprises a zonal structure that stretches out from barrel-like structure.RNA combines with two parts of L14.The far-end of RNA binding site identification ribosome-RNA(rRNA) in the ribosomal particle assembling.Second RNA binding site after RNA occupied when tightening.The hydrophobic part on L14 surface may be the site of protein-protein interaction, for example with L19 albumen.[Christopher?Davis?et?al，Structure?Vol4，No.1，15?Jan?1996]
The disappearance of ribosomal protein or inappropriate chemically modified, or the gene of ribosomal protein is undergone mutation, all will influence ribosomal function, reduce polypeptide synthetic activity, thereby cause various serious consequences, for example membrane structure can not be kept, cellular metabolism is not normal, cell surface antibody reduces, the cell growth pauses even dead or the like, causes various diseases thus, for example grows disorder, metabolic trouble, Immunological diseases, necrocytosis or the like.
The present invention has 27% homology with the L14 albumen of finding on protein level in fruit bat, thus think that gene of the present invention is the gene of a coding and L14 protein similar, and have similar biological function.Called after human protein synthetic protein L23 of the present invention.
Because human protein synthetic protein L14.22 albumen plays an important role in regulating body critical functions such as cell fission and fetal development as mentioned above, and believe and relate to a large amount of albumen in these regulate processes, thereby need to identify the human protein synthetic protein L14.22 albumen of more these processes of participation in this area always, particularly identify this proteic aminoacid sequence.The separation of new human protein synthetic protein L14.22 protein coding gene also provides the foundation for determining the effect of this albumen under healthy and morbid state.This albumen may constitute the basis of exploitation medical diagnosis on disease and/or curative, and it is very important therefore separating its coding DNA.
Summary of the invention
An object of the present invention is to provide isolating new polypeptide-human protein synthetic protein L14.22 with and fragment, analogue and derivative.
Another object of the present invention provides the polynucleotide of this polypeptide of coding.
Another object of the present invention provides the recombinant vectors of the polynucleotide that contain coding human protein synthetic protein L14.22.
Another object of the present invention provides the genetically engineered host cell of the polynucleotide that contain coding human protein synthetic protein L14.22.
Another object of the present invention provides the method for producing human protein synthetic protein L14.22.
Another object of the present invention provides the antibody at polypeptide-human protein synthetic protein L14.22 of the present invention.
The present invention relates to a kind of isolated polypeptide, this polypeptide is the people source, and it comprises: have＜polypeptide or its examples of conservative variations, bioactive fragment or the derivative of 210〉2 aminoacid sequences.Preferably, this polypeptide is to have＜polypeptide of 210〉2 aminoacid sequences.
The invention still further relates to a kind of isolating polynucleotide, it comprises a kind of nucleotide sequence or its variant that is selected from down group:
(a) coding has＜polynucleotide of the polypeptide of 210〉2 aminoacid sequences;
(b) with polynucleotide (a) complementary polynucleotide;
(c) with (a) or polynucleotide sequence (b) have the polynucleotide of at least 70% homogeny.
More preferably, the sequence of these polynucleotide is be selected from down group a kind of: (a) have＜210〉1 in the sequence of 413-1024 position; (b) have＜210〉1 in the sequence of 1-2002 position.
The present invention relates to a kind of carrier that contains polynucleotide of the present invention, particularly expression vector in addition; The host cell that this carrier of a kind of usefulness is genetically engineered comprises the host cell of conversion, transduction or transfection; A kind of method for preparing polypeptide of the present invention of cultivating described host cell and reclaiming expression product that comprises.
The invention still further relates to a kind of can with polypeptid specificity bonded antibody of the present invention.
Others of the present invention are because disclosing of the technology of this paper is conspicuous to those skilled in the art.
The invention provides a kind of polypeptide-human protein synthetic protein L14.22, it is basically by＜210〉aminoacid sequence shown in 2 forms.Polypeptide of the present invention can be recombinant polypeptide, natural polypeptides, synthetic polypeptide, preferred recombinant polypeptide.Polypeptide of the present invention can be the product of natural purifying, or the product of chemosynthesis, or uses recombinant technology to produce from protokaryon or eucaryon host (for example, bacterium, yeast, higher plant, insect and mammalian cell).The host used according to the recombinant production scheme, polypeptide of the present invention can be glycosylated, maybe can be nonglycosylated.Polypeptide of the present invention also can comprise or not comprise initial methionine residues.
The present invention also comprises fragment, derivative and the analogue of human protein synthetic protein L14.22.As used herein, term " fragment ", " derivative " are meant with " analogue " and keep identical biological function of human protein synthetic protein L14.22 of the present invention or active polypeptide basically.The fragment of polypeptide of the present invention, derivative or analogue can be: (I) a kind of like this, wherein one or more amino-acid residues are replaced by conservative or non-conservative amino acid residues (preferably conservative amino acid residues), and the amino acid that replaces can be also can not encoded by genetic codon; Perhaps (II) is a kind of like this, and certain group on wherein one or more amino-acid residues is replaced by other group and comprises substituting group; Perhaps (III) is a kind of like this, and wherein mature polypeptide and another kind of compound (such as the compound that prolongs the polypeptide transformation period, for example polyoxyethylene glycol) merge; Perhaps (IV) is a kind of like this, wherein additional aminoacid sequence is integrated into mature polypeptide and the peptide sequence that forms (as leader sequence or secretion sequence or be used for the sequence or the proteinogen sequence of this polypeptide of purifying) by the elaboration of this paper, such fragment, derivative and analogue are considered within those skilled in the art's ken.
The invention provides isolating nucleic acid (polynucleotide), substantially by coding have＜polynucleotide of the polypeptide of 210〉2 aminoacid sequences form.Polynucleotide sequence of the present invention comprises＜210〉1 nucleotide sequence.Polynucleotide of the present invention are to find from the cDNA library of people's fetal brain tissue.The polynucleotide sequence total length that it comprises is 2002 bases, its open reading frame (413-1024) 203 amino acid of having encoded.Find relatively that according to amino acid sequence homologous this polypeptide and L14 albumen have 27% homology, deducibility goes out the 26S Proteasome Structure and Function that this human protein synthetic protein L14.22 has the L14 protein similar.
Polynucleotide of the present invention can be dna form or rna form.Dna form comprises the DNA of cDNA, genomic dna or synthetic.DNA can be strand or double-stranded.DNA can be coding strand or noncoding strand.The coding region sequence of encoding mature polypeptide can be identical with the coding region sequence shown in＜210〉1 or the varient of degeneracy.As used herein, " varient of degeneracy " are meant that in the present invention coding has＜210〉2 protein or polypeptide, but with the differentiated nucleotide sequence of coding region sequence shown in＜210〉1.
The polynucleotide of the mature polypeptide of coding＜210〉2 comprise: the encoding sequence that has only mature polypeptide; The encoding sequence of mature polypeptide and various additional code sequence; Encoding sequence of mature polypeptide (with optional additional code sequence) and non-coding sequence.
Term " polynucleotide of coded polypeptide " is meant polynucleotide that comprise this polypeptide of encoding and the polynucleotide that comprise additional code and/or non-coding sequence.
The invention still further relates to the varient of foregoing description polynucleotide, its coding has the polypeptide of identical aminoacid sequence or segment, analogue and the derivative of polypeptide with the present invention.The varient of these polynucleotide can be the allelic variant of natural generation or the varient that non-natural takes place.These nucleotide diversity bodies comprise and replace varient, deletion mutation body and insert varient.As known in the art, allelic variant is the replacement form of polynucleotide, and it may be replacement, disappearance or the insertion of one or more Nucleotide, but can be from not changing the function of its encoded polypeptides in fact.
The invention still further relates to and the polynucleotide (have at least 50% between two sequences, preferably have 70% homogeny) of sequence hybridization described above.The present invention be more particularly directed under stringent condition and the interfertile polynucleotide of polynucleotide of the present invention.In the present invention, " stringent condition " is meant: (1) than hybridization under low ionic strength and the comparatively high temps and wash-out, as 0.2 * SSC, and 0.1%SDS, 60 ℃; Or (2) hybridization the time adds and to use denaturing agent, as 50% (v/v) methane amide, 0.1% calf serum/0.1%Ficoll, 42 ℃ etc.; Or (3) only at the homogeny between the two sequences at least more than 95%, be more preferably 97% and just hybridize when above.And, the polypeptide of interfertile polynucleotide encoding and＜210〉and the mature polypeptide shown in 2 has identical biological function and activity.
The invention still further relates to nucleic acid fragment with sequence hybridization described above.As used herein, " nucleic acid fragment " length contain 10 Nucleotide at least, better be 20-30 Nucleotide at least, be more preferably 50-60 Nucleotide at least, preferably more than at least 100 Nucleotide.Nucleic acid fragment also can be used for the amplification technique (as PCR) of nucleic acid to determine and/or to separate the polynucleotide of coding human protein synthetic protein L14.22.
Polypeptide among the present invention and polynucleotide preferably provide with isolating form, more preferably are purified to homogeneous.
The special polynucleotide sequence of coding human protein synthetic protein L14.22 of the present invention can obtain with several different methods.For example, separate polynucleotide with hybridization technique well known in the art.These technology including, but not limited to: 1) with probe and genome or the hybridization of cDNA library to detect homologous polynucleotide sequence and 2) antibody screening of expression library to be to detect the polynucleotide passage of the clone with common structure feature.
Sequence dna fragment of the present invention also can obtain with following method: 1) separate double chain DNA sequence from genomic dna; 2) the chemical synthesising DNA sequence is to obtain the double-stranded DNA of described polypeptide.
In the above-mentioned method of mentioning, isolation of genomic DNA is least commonly used.The direct chemical of dna sequence dna is synthetic to be the method for often selecting for use.The more frequent method of selecting for use is the separation of cDNA sequence.The standard method that separates interested cDNA is from the donorcells separating mRNA of this gene of high expression level and carries out reverse transcription, forms plasmid or phage cDNA library.Extract the existing multiple proven technique of method of mRNA, test kit also can obtain (Qiagene) from commercial channels.And the construction cDNA library also is usual method (Sambrook, et al., MolecularCloning, A Laboratory Manual, Cold Spring Harbor Laboratory.New YorK, 1989).Also can obtain the cDNA library of commercial offers, as the different cDNA library of Clontech company.When being used in combination the polymeric enzyme reaction technology, even few expression product also can be cloned.
Available ordinary method is screened gene of the present invention from these cDNA libraries.These methods include, but is not limited to: (1) DNA-DNA or DNA-RNA hybridization; (2) appearance of marker gene function or forfeiture; (3) level of the transcript of mensuration human protein synthetic protein L14.22; (4), detect the protein product of genetic expression by immunological technique or mensuration biologic activity.Aforesaid method can singly be used, but also several different methods combined utilization.
In (1) kind method, hybridizing used probe is and any a part of homology of polynucleotide of the present invention that at least 10 Nucleotide of its length better are at least 30 Nucleotide, are more preferably at least 50 Nucleotide, preferably at least 100 Nucleotide.In addition, within 2000 Nucleotide, preferable is within 1000 Nucleotide to the length of probe usually.Probe used herein is the dna sequence dna of chemosynthesis on the basis of gene order information of the present invention normally.Gene of the present invention itself or fragment are certainly as probe.The mark of dna probe can be used radio isotope, fluorescein or enzyme (as alkaline phosphatase) etc.
In (4) kind method, detect the protein product of human protein synthetic protein L14.22 genetic expression and can use immunological technique such as Western blotting, radioimmunoprecipitation, enzyme-linked immunosorbent assay (ELISA) etc.
Use method (Saiki, the et al.Science1985 of round pcr DNA amplification/RNA; 230:1350-1354) be optimized for acquisition gene of the present invention.When particularly being difficult to from the library, obtain the cDNA of total length, can preferably use RACE method (the terminal rapid amplifying method of RACE-cDNA), the primer that is used for PCR can suitably be selected according to polynucleotide sequence information of the present invention disclosed herein, and available ordinary method is synthetic.Available ordinary method is as the DNA/RNA fragment by gel electrophoresis separation and purifying amplification.
The gene of the present invention that obtains as mentioned above, perhaps the polynucleotide sequence of various dna fragmentations etc. can with ordinary method such as dideoxy chain termination (Sanger et al.PNAS, 1977,74:5463-5467) measure.This class polynucleotide sequence is measured also available commercial sequencing kit etc.In order to obtain the cDNA sequence of total length, order-checking need be carried out repeatedly.Sometimes need to measure a plurality of clones' cDNA sequence, just can be spliced into the cDNA sequence of total length.
The present invention also relates to comprise the carrier of polynucleotide of the present invention, and with carrier of the present invention or directly with the host cell of human protein synthetic protein L14.22 encoding sequence through the genetically engineered generation, and the method that produces polypeptide of the present invention through recombinant technology.
Among the present invention, the polynucleotide sequence of coding human protein synthetic protein L14.22 can be inserted in the carrier, contains the recombinant vectors of polynucleotide of the present invention with formation.Term " carrier " refers to that bacterial plasmid well known in the art, phage, yeast plasmid, vegetable cell virus, mammalian cell virus are as adenovirus, retrovirus or other carrier.The carrier of Shi Yonging includes but not limited in the present invention: and the expression vector based on the T7 promotor of in bacterium, expressing (Rosenberg, et al.Gene, 1987,56:125); The pMSXND expression vector of in mammalian cell, expressing (Lee and Nathans, J Bio Chem.263:3521,1988) and at the carrier that derives from baculovirus of expressed in insect cells.In a word, as long as can duplicate in host and stablize, any plasmid and carrier may be used to make up recombinant expression vector.A key character of expression vector is to contain replication origin, promotor, marker gene and translational control element usually.
Method well-known to those having ordinary skill in the art can be used to make up the dna sequence dna that contains coding human protein synthetic protein L14.22 and the expression vector of suitable transcribing/translational control element.These methods comprise (Sambroook, et al.Molecular Cloning, aLaboratory Manual, cold Spring Harbor Laboratory.New York, 1989) such as extracorporeal recombinant DNA technology, DNA synthetic technology, the interior recombinant technologys of body.Described dna sequence dna can effectively be connected on the suitable promotor in the expression vector, and is synthetic to instruct mRNA.The representative example of these promotors has: colibacillary lac or trp promotor; The P of lambda particles phage
LPromotor; Eukaryotic promoter comprises LTRs and some other known may command gene expression promoter in prokaryotic cell prokaryocyte or eukaryotic cell or its virus of CMV immediate early promoter, HSV thymidine kinase promoter, early stage and late period SV40 promotor, retrovirus.Expression vector also comprises ribosome bind site that translation initiation is used and transcription terminator etc.Inserting enhancer sequence in carrier will make its transcribing in higher eucaryotic cells be enhanced.Enhanser is the cis acting factor that DNA expresses, and nearly 10 to 300 base pairs act on promotor transcribing with enhancing gene usually.Can for example be included in the SV40 enhanser of 100 to 270 base pairs of replication origin side in late period one, at the polyoma enhanser of replication origin side in late period one and adenovirus enhanser etc.
In addition, expression vector preferably comprises one or more selected markers, to be provided for selecting the phenotypic character of transformed host cells, cultivate Tetrahydrofolate dehydrogenase, neomycin resistance and the green fluorescent protein (GFP) of usefulness as eukaryotic cell, or be used for colibacillary tsiklomitsin or amicillin resistance etc.
Persons skilled in the art all know how to select appropriate carriers/transcriptional regulatory element (as promotor, enhanser etc.) and selected marker.
Among the present invention, the polynucleotide of coding human protein synthetic protein L14.22 or the recombinant vectors that contains these polynucleotide can transform or transduce into host cell, contain the genetically engineered host cell of these polynucleotide or recombinant vectors with formation.Term " host cell " refers to prokaryotic cell prokaryocyte, as bacterial cell; Or eukaryotic cell such as low, as yeast cell; Or higher eucaryotic cells, as mammalian cell.Representative example has: intestinal bacteria, streptomyces; Bacterial cell such as Salmonella typhimurium; Fungal cell such as yeast; Vegetable cell; Insect cell such as fruit bat S2 or Sf9; Zooblast such as CHO, COS or Bowes melanoma cells etc.
Can carry out with routine techniques well known to those skilled in the art with dna sequence dna of the present invention or the recombinant vectors transformed host cell that contains described dna sequence dna.When the host was prokaryotic organism such as intestinal bacteria, the competent cell that can absorb DNA can be used CaCl in exponential growth after date results
2Method is handled, and used step is well-known in this area.Alternative is to use MgCl
2If desired, transforming also the method for available electroporation carries out.When the host is an eukaryote, can select following DNA transfection method for use: coprecipitation of calcium phosphate method, perhaps conventional mechanical method such as microinjection, electroporation, liposome packing etc.
By the recombinant DNA technology of routine, utilize polynucleotide sequence of the present invention to can be used to express or produce human protein synthetic protein L14.22 (Science, 1984 of reorganization; 224:1431).In general following steps are arranged:
(1). with the polynucleotide (or varient) of coding of the present invention people human protein synthetic protein L14.22, or with the recombinant expression vector that contains these polynucleotide proper host cell that transforms or transduce;
(2). in suitable medium, cultivate host cell;
(3). separation, protein purification from substratum or cell.
In step (2), according to used host cell, used substratum can be selected from various conventional substratum in the cultivation.Under the condition that is suitable for the host cell growth, cultivate.After host cell grows into suitable cell density, induce the promotor of selection with suitable method (as temperature transition or chemical induction), cell is cultivated for some time again.
In step (3), recombinant polypeptide can wrap and be expressed or be secreted into the extracellular in cell or on cytolemma.If desired, can utilize its physics, the separating by various separation methods with other characteristic and the albumen of purification of Recombinant of chemistry.These methods are well-known to those skilled in the art.These methods include, but are not limited to: conventional renaturation is handled, protein precipitant is handled (salt analysis method), centrifugal, the broken bacterium of infiltration, the combination of ultrasonication, super centrifugal, sieve chromatography (gel-filtration), adsorption chromatography, ion exchange chromatography, high performance liquid chromatography (HPLC) and other various liquid chromatography (LC) technology and these methods.
The present invention also provides SCREENED COMPOUND to identify the method that improves (agonist) or check the medicament of (antagonist) human protein synthetic protein L14.22.Agonist improves human protein synthetic protein L14.22 biological function such as stimulate cellular proliferation, and antagonist prevention disorder such as the various cancer relevant with cell hyperproliferation with treatment.For example, can be in the presence of medicine, the human protein synthetic protein L14.22 with mark cultivates with the film preparation of mammalian cell or expressing human protein synthetic protein L14.22.Measure the medicine raising then or check this interactional ability.
The antagonist of human protein synthetic protein L14.22 comprises antibody, compound, acceptor disappearance thing and the analogue etc. that filter out.The antagonist of human protein synthetic protein L14.22 can combine and eliminate its function with human protein synthetic protein L14.22, or suppresses the generation of this polypeptide, or combines with the avtive spot of this polypeptide and to make this polypeptide can not bring into play biological function.
In screening during as the compound of antagonist, human protein synthetic protein L14.22 can be added in the bioanalysis mensuration, interactional influence between human protein synthetic protein L14.22 and its acceptor be determined whether compound is antagonist by measuring compound.With the same quadrat method of above-mentioned SCREENED COMPOUND, can filter out the acceptor disappearance thing and the analogue of antagonist action.Can be incorporated into the rondom polypeptide storehouse that solid formation forms by the various amino acid that may make up by screening with human protein synthetic protein L14.22 bonded peptide molecule obtains.During screening, generally tackle human protein synthetic protein L14.22 molecule and carry out mark.
The invention provides and use polypeptide, and fragment, derivative, analogue or their cell are as the method for antigen with production antibody.These antibody can be polyclonal antibody or monoclonal antibody.The present invention also provides the antibody at human protein synthetic protein L14.22 antigenic determinant.These antibody include, but is not limited to: the fragment that polyclonal antibody, monoclonal antibody, chimeric antibody, single-chain antibody, Fab fragment and Fab expression library produce.
The method of the available human protein synthetic protein L14.22 of the production of polyclonal antibody direct injection immune animal (as rabbit, mouse, rat etc.) obtains, and multiple adjuvant can be used for the enhancing immunity reaction, includes but not limited to freund's adjuvant etc.The technology of the monoclonal antibody of preparation human protein synthetic protein L14.2 2 include but not limited to hybridoma technology (Kohler and Milstein.Nature, 1975,256:495-497), three knurl technology, people B-quadroma technology, EBV-hybridoma technology etc.With the variable region bonded chimeric antibody in human constant region and inhuman source can with existing technology production (Morrison et al, PNAS, 1985,81:6851).And the technology of existing manufacture order chain antibody (U.S.Pat No.4946778) also can be used for producing the single-chain antibody of anti-human protein synthetic protein L14.22.
The antibody of anti-human protein synthetic protein L14.22 can be used in the immunohistochemistry technology, detects the human protein synthetic protein L14.22 in the biopsy specimen.
With the also available labelled with radioisotope of human protein synthetic protein L14.22 bonded monoclonal antibody, inject in the body and can follow the tracks of its position and distribution.This radiolabeled antibody can be used as a kind of atraumatic diagnostic method and is used for the location of tumour cell and has judged whether transfer.
Antibody also can be used for designing the immunotoxin at a certain privileged sites in the body.As the monoclonal antibody of human protein synthetic protein L14.22 high-affinity can with bacterium or plant poison (as diphtheria toxin, ricin, abrine etc.) covalent attachment.A kind of usual method is with sulfydryl linking agent such as SPDP, attacks the amino of antibody, by the exchange of disulfide linkage, toxin is incorporated on the antibody, and this hybrid antibody can be used for killing human protein synthetic protein L14.22 positive cells.
The disease that antibody among the present invention can be used for treating or prevention is relevant with human protein synthetic protein L14.22.The antibody that gives suitable dosage can stimulate or block generation or the activity of human protein synthetic protein L14.22.
The invention still further relates to the diagnostic testing process of quantitative and detection and localization human protein synthetic protein L14.22 level.These tests are known in the art, and comprise that FISH measures and radioimmunoassay.The human protein synthetic protein L14.22 level that is detected in the test can be with laying down a definition the importance of human protein synthetic protein L14.22 in various diseases and be used to the disease of diagnosing human protein synthetic protein L14.22 to work.
Polypeptide of the present invention also can be used as the peptide spectrum analysis, for example, the polypeptide available physical, chemistry or enzyme carry out the specificity cutting, and carries out the two-dimentional or three-dimensional gel electrophoresis analysis of one dimension, be more preferably and carry out mass spectroscopy.
The polynucleotide of coding human protein synthetic protein L14.22 also can be used for multiple therapeutic purpose.Gene therapy technology can be used for treating because cell proliferation, growth or the metabolic disturbance due to the nothing expression of human protein synthetic protein L14.22 or the unusual/non-activity expression.The gene therapy vector (as virus vector) of reorganization can be designed for the human protein synthetic protein L14.22 that expresses variation, to suppress endogenic human protein synthetic protein L14.22 activity.For example, a kind of human protein synthetic protein L14.22 of variation can be the human protein synthetic protein L14.22 that shortens, lacked signal conduction function territory, though can combine with the substrate in downstream, lacks signaling activity.Therefore the gene therapy vector of reorganization can be used for treating the disease of human protein synthetic protein L14.22 expression or active caused by abnormal.Deriving from viral expression vector such as retrovirus, adenovirus, adeno-associated virus (AAV), hsv, parvovirus etc. can be used for the polynucleotide of coding human protein synthetic protein L14.22 are transferred in the cell.The method of recombinant viral vector that structure carries the polynucleotide of coding human protein synthetic protein L14.22 is found in existing document (Sambrook, et al.).The polynucleotide of reorganization coding human protein synthetic protein L14.22 can be packaged in the liposome and be transferred in the cell in addition.
Polynucleotide import tissue or intracellular method comprises: directly be injected into polynucleotide in the in-vivo tissue; Or external by carrier (as virus, phage or plasmid etc.) earlier with the polynucleotide transfered cell in, again cell is transplanted in the body etc.
Suppress the oligonucleotide (comprising sense-rna and DNA) of human protein synthetic protein L14.22mRNA and ribozyme also within the scope of the invention.Ribozyme is the enzyme sample RNA molecule that a kind of energy specificity is decomposed specific RNA, and its mechanism of action is to carry out the endonuclease effect after ribozyme molecule and the hybridization of complementary target RNA-specific.The RNA of antisense and DNA and ribozyme can obtain with existing any RNA or DNA synthetic technology, as the technology widespread use of solid phase phosphoamide chemical synthesis synthetic oligonucleotide.Antisense rna molecule can be transcribed acquisition by the dna sequence dna of this RNA that encodes in external or body.This dna sequence dna has been incorporated into the downstream of rna polymerase promoter of carrier.In order to increase the stability of nucleic acid molecule, available several different methods is modified it, and as increasing the sequence length of both sides, the connection between the ribonucleoside is used phosphoric acid thioester bond or peptide bond but not phosphodiester bond.
The polynucleotide of coding human protein synthetic protein L14.22 can be used for the diagnosis with the relative disease of human protein synthetic protein L14.22.The unconventionality expression of the expression that the polynucleotide of coding human protein synthetic protein L14.22 can be used for detecting human protein synthetic protein L14.22 human protein synthetic protein L14.22 whether or under morbid state.As the dna sequence dna of the human protein synthetic protein L14.22 that encodes can be used for biopsy specimen is hybridized to judge the expression situation of human protein synthetic protein L14.22.Hybridization technique comprises the Southern blotting, Northern blotting, in situ hybridization etc.These technological methods all are disclosed mature technologies, and relevant test kit all can obtain from commercial channels.Part or all of polynucleotide of the present invention can be used as probe stationary on microarray (Microarray) or DNA chip (being called " gene chip " again), is used for analyzing the differential expression analysis and the gene diagnosis of tissue gene.Carry out the transcription product that RNA-polymerase chain reaction (RT-PCR) amplification in vitro also can detect human protein synthetic protein L14.22 with the special primer of human protein synthetic protein L14.22.
The sudden change that detects human protein synthetic protein L14.22 gene also can be used for the disease of diagnosing human protein synthetic protein L14.22 relevant.The form of human protein synthetic protein L14.22 sudden change comprises that the point mutation compared with normal wild type human protein synthetic protein L14.22DNA sequence, transposition, disappearance, reorganization and other are any unusual etc.Available existing technology such as Southern blotting, dna sequence analysis, PCR and in situ hybridization detect sudden change.In addition, sudden change might influence proteic expression, therefore can judge indirectly that with Northern blotting, Western blotting gene has or not sudden change.
Sequence of the present invention identifies it also is valuable to karyomit(e).This sequence can be specifically at certain bar human chromosome particular location and and can with its hybridization.At present, need to identify the concrete site of each gene on the karyomit(e).Now, have only chromosomal marker thing seldom to can be used for the marker chromosomes position based on actual sequence data (repetition polymorphism).According to the present invention, for these sequences are associated with disease related gene, its important the first step is positioned these dna sequence dnas on the karyomit(e) exactly.
In brief, prepare PCR primer (preferred 15-35bp), sequence can be positioned on the karyomit(e) according to cDNA.Then, these primers are used for the somatocyte hybrid cell that the PCR screening contains each bar human chromosome.Have only those hybrid cells that contain corresponding to the people's gene of primer can produce the fragment of amplification.
The PCR localization method of somatocyte hybrid cell is that DNA is navigated to concrete chromosomal quick method.Use Oligonucleolide primers of the present invention,, can utilize one group to realize inferior location from specific chromosomal fragment or a large amount of genomic clone by similar approach.Other the similar strategy that can be used for chromosomal localization comprises in situ hybridization, uses the karyomit(e) prescreen and the hybridization preliminary election of the airflow classification of mark, thereby makes up the special cDNA storehouse of karyomit(e).
The cDNA clone is carried out fluorescence in situ hybridization (FISH) with Metaphase Chromosome, can in a step, accurately carry out chromosomal localization.The summary of this technology is referring to Verma etc., Human Chromosomes:a Manualof Basic Techniques, Pergamon Press, New York (1988).
In case sequence is positioned to chromosome position accurately, the physical location of this sequence on karyomit(e) just can be associated with the gene map data.These data for example are found in, V.Mckusick, Mendelian Inheritancein Man (can by with the online acquisition of Johns Hopkins Uniyersity Welch Medical Library).Can pass through linkage analysis then, determine gene and navigated to relation between the disease on the chromosomal region already.
Then, need to measure ill and not cDNA between diseased individuals or genome sequence difference.If observe certain sudden change in some or all of diseased individuals, and this sudden change is not observed in any normal individual, then this sudden change may be the cause of disease of disease.More ill and diseased individuals not is usually directed at first seek the variation of structure in the karyomit(e), as from the horizontal visible of karyomit(e) or use based on detectable disappearance of the PCR of cDNA sequence or transposition.Resolving power according to present physical mapping and assignment of genes gene mapping technology, being accurately positioned to the cDNA of the chromosomal region relevant with disease, can be a kind of (the supposing that 1 megabasse mapping resolving power and every 20kb are corresponding to a gene) between 50 to 500 potential Disease-causing genes.
Polypeptide of the present invention, polynucleotide and stand-in thereof, agonist, antagonist and inhibitor and suitable pharmaceutical carrier combination back can be used.These carriers can be water, glucose, ethanol, salt, damping fluid, glycerine and their combination.Composition comprises the polypeptide or the antagonist of safe and effective amount and carrier and the vehicle that does not influence effect of drugs.These compositions can be used as medicine and are used for disease treatment.
The present invention also provides medicine box or the test kit that contains one or more containers, and one or more medicinal compositions compositions of the present invention are housed in the container.With these containers, can have by the given indicative prompting of government authorities of making, using or selling medicine or biological products, the government authorities that this prompting reflects production, uses or sells permits it to use on human body.In addition, polypeptide of the present invention can be used in combination with other treatment compound.
Pharmaceutical composition can be with mode administration easily, as by in part, intravenously, intraperitoneal, intramuscular, subcutaneous, the nose or the route of administration of intracutaneous.Human protein synthetic protein L14.22 comes administration with the amount that treats and/or prevents concrete indication effectively.The amount and the dosage range that are applied to patient's human protein synthetic protein L14.22 will depend on many factors, as administering mode, person's to be treated healthiness condition and diagnostician's judgement.
Description of drawings
Following accompanying drawing is used to illustrate specific embodiments of the present invention, and is not used in qualification by the scope of the invention that claims defined.
Fig. 1 is the proteic amino acid sequence homology comparison diagram of inventor's protein synthetic protein L14.22 and L14.The top sequence is human protein synthetic protein L14.22, and the below sequence is a L14 albumen.Same amino acid represents with monocase amino acid that between two sequences similar amino acid is represented with "+".
Fig. 2 is the polyacrylamide gel electrophoresis figure (SDS-PAGE) of isolating human protein synthetic protein L14.22.22kDa is proteinic molecular weight.The arrow indication is isolated protein band.
Embodiment
Below in conjunction with specific embodiment, further set forth the present invention.Should be understood that these embodiment only to be used to the present invention is described and be not used in and limit the scope of the invention.The experimental technique of unreceipted actual conditions in the following example, usually according to people such as normal condition such as Sambrook, molecular cloning: laboratory manual (New York:Cold SpringHarbor Laboratory Press, 1989) condition described in, or the condition of advising according to manufacturer.
Embodiment 1: the clone of human protein synthetic protein L14.22
Extract the total RNA of people's tire brain with guanidinium isothiocyanate/phenol/chloroform single stage method.From total RNA, separate poly (A) mRNA with Quik mRNA Isolation Kit (Qiegene company product).2ug poly (A) mRNA forms cDNA through reverse transcription.CDNA fragment orientation is inserted on the multiple clone site of pBSK (+) carrier (Clontech company product) with Smart cDNA clone's test kit (available from Clontech), transforms DH5 α, bacterium forms the cDNA library.Measure all clones' 5 ' and 3 ' terminal sequence with Dyeterminate cycle reaction sequencing kit (Perkin-Elmer company product) and ABI 377 automatic sequencers (Perkin-Elmer company).CDNA sequence and the existing public dna sequence data storehouse (Genebank) measured are compared, found that the cDNA sequence of one of them clone 0507E08 is new DNA.By synthetic a series of primers the contained insertion cDNA fragment of this clone is carried out two-way mensuration.The result shows, the contained full-length cDNA of 0507E08 clone is 2002bp (as＜210〉1 shown in), from 413bp to 1024bp the open reading frame (ORF) of a 612bp arranged, the new protein of encoding (as＜210〉2 shown in).We are with this clone's called after pBS-0507E08, encoded protein matter called after human protein synthetic protein L14.22.
Embodiment 2:cDNA clone's homology retrieval
With sequence and the encoded protein sequence thereof of human protein synthetic protein L14.22 of the present invention, with Blast program (Basiclocal Alignment search tool) [Altschul, SF et al.J.Mol.Biol.1990; 215:403-10], carry out the homology retrieval at databases such as Genbank, Swissport.The gene the highest with human protein synthetic protein L14.22 homology of the present invention is a kind of known L14 albumen, and its encoded protein number is Y10018 in the access of Genbank.Protein homology the results are shown in Fig. 1, both height homologies, and its homogeny is 27%; Similarity is 52%.
Embodiment 3: with the gene of RT-PCR method clones coding human protein synthetic protein L14.22
Total RNA is a template with fetus brain cell, is that primer carries out the synthetic cDNA of reverse transcription reaction with oligo-dT, with behind the test kit purifying of Qiagene, carries out pcr amplification with following primer:
Primer1：5’-GACGGTTAACTTTGACCCAAAGAC-3’(<210>3)
Primer2：5’-GCTTTCAAGCAGTCTTTACTTGGG-3’(<210>4)
Primer1 for to be positioned at＜the forward sequence that begins of 1bp of 210〉15 ' end;
Primer2 be＜210〉1 in 3 ' end reverse sequence.
The condition of amplified reaction: in the reaction volume of 50 μ l, contain 50mmol/L KCl, 10mmol/LTris-Cl, (pH8.5), 1.5mmol/L MgCl
2, 200 μ mol/L dNTP, 10pmol primer, the Taq archaeal dna polymerase of 1U (Clontech company product).Go up by 25 cycles of following conditioned response at PE9600 type DNA thermal cycler (Perkin-Elmer company): 94 ℃ of 30sec; 55 ℃ of 30sec; 72 ℃ of 2min.When RT-PCR, establish the blank negative contrast of positive contrast of β-actin and template simultaneously.Amplified production is connected to (Invitrogen company product) on the pCR carrier with the test kit purifying of QIAGEN company with TA clone test kit.The dna sequence analysis result shows the dna sequence dna and＜210 of PCR product〉1-2002bp shown in 1 is identical.
Embodiment 4:Northern blotting analyst protein synthetic protein L14.22 expression of gene:
Extract total RNA[Anal.Biochem 1987,162,156-159 with single stage method].This method comprises acid guanidine thiocyanate phenol-chloroform extracting.Promptly use 4M guanidinium isothiocyanate-25mM Trisodium Citrate, 0.2M sodium acetate (pH4.0) carries out homogenate to tissue, adds the phenol of 1 times of volume and the chloroform-primary isoamyl alcohol (49: 1) of 1/5 volume, and is centrifugal after mixing.The sucking-off aqueous phase layer adds Virahol (0.8 volume) and with the centrifugal RNA precipitation that obtains of mixture.With RNA precipitation 70% washing with alcohol that obtains, dry and soluble in water.With 20 μ g RNA, on 1.2% sepharose that contains 20mM 3-(N-morpholino) propanesulfonic acid (pH7.0)-5mM sodium acetate-1mM EDTA-2.2M formaldehyde, carry out electrophoresis.Be transferred on the nitrocellulose filter then.With α-
32P dATP prepares by random priming
32The dna probe of P-mark.Used dna probe is the human protein synthetic protein L14.22 coding region sequence (413bp to 1024bp) of pcr amplification shown in Figure 1.Probe (about 2 * 10 with the 32P-mark
6Cpm/ml) spend the night in 42 ℃ of hybridization in a solution with the nitrocellulose filter that has shifted RNA, this solution comprises 50% methane amide-25mM KH
2PO
4(pH7.4)-5 * SSC-5 * Denhardt ' s solution and 200 μ g/ml salmon sperm DNAs.After the hybridization, filter membrane is washed 30min in 55 ℃ in 1 * SSC-0.1%SDS.Then, analyze with quantitative with Phosphor Imager.
Embodiment 5: vivoexpression, separation and the purifying of recombinant human protein's synthetic proteins L14.22
According to＜210〉1 and coding region sequence shown in Figure 1, design a pair of specificity amplification primer, sequence is as follows:
Primer3：5’-CCCCATATGATGTACCTGTTTCCCAGGCAACTAC-3’(<210>5)
Primer4：5’-CATGGATCCTCAGCGCCTTGTCCCAAGGTAGTTG-3’(<210>6)
5 ' end of these two sections primers contains NdeI and BamHI restriction enzyme site respectively, be respectively the encoding sequence of target gene 5 ' end and 3 ' end thereafter, NdeI and BamHI restriction enzyme site are corresponding to expression vector plasmid pET-28b (+) (Novagen company product, Cat.No.69865.3) the selectivity restriction enzyme site on.With the pBS-0507E08 plasmid that contains the total length goal gene is template, carries out the PCR reaction.The PCR reaction conditions is: contain pBS-0507E08 plasmid 10pg, primer Primer-3 and Primer-4 among the cumulative volume 50 μ l and be respectively 10pmol, Advantage polymerase Mix (Clontech company product) 1 μ l.Loop parameter: 94 ℃ of 20s, 60 ℃ of 30s, 68 ℃ of 2min, totally 25 circulations.Respectively amplified production and plasmid pET-28 (+) are carried out double digestion with NdeI and BamHI, reclaim big fragment respectively, and connect with the T4 ligase enzyme.Connect product and transform, after the dull and stereotyped overnight incubation of the LB that contains kantlex (final concentration 30 μ g/ml), use the colony polymerase chain reaction (PCR) method screening positive clone, and check order with the big enterobacterial DH5 of Calcium Chloride Method α.Select the correct positive colony of sequence (pET-0507E08) with Calcium Chloride Method with recombinant plasmid transformed e. coli bl21 (DE3) plySs (Novagen company product).In the LB liquid nutrient medium that contains kantlex (final concentration 30 μ g/ml), host bacterium BL21 (pET-0507E08) is cultured to logarithmic phase at 37 ℃, adds IPTG to final concentration 1mmol/L, continues to cultivate 5 hours.Centrifugal collection thalline, through the broken bacterium of ultrasonic wave, centrifugal collection supernatant with carrying out chromatography with 6 Histidines (6His-Tag) bonded affinity column His.Bind Quick Cartridge (Novagen company product), has obtained the target protein human protein synthetic protein L14.22 of purifying.Through the SDS-PAGE electrophoresis, obtain a single band (Fig. 2) at the 22kDa place.This band is transferred on the pvdf membrane carries out the n terminal amino acid sequential analysis with the Edams hydrolysis method, 15 amino acid of N-end are identical with 15 amino-acid residues of N-end shown in＜210〉2 as a result.
Embodiment 6 anti-human protein synthetic protein L14.22 production of antibodies
With the synthetic specific polypeptide of following human protein synthetic protein L14.22: the NH of Peptide synthesizer (PE company product)
2-Met-Tyr-Leu-Phe-Pro-Arg-Gln-Leu-Leu-Ile-Arg-His-Phe-Trp-Thr-COOH
Form compoundly with hemocyanin and bovine serum albumin coupling this polypeptide respectively, method is referring to Avrameas, etal.Immunochemistry, 1969; 6:43.Add the complete Freund's adjuvant immunizing rabbit with the above-mentioned hemocyanin polypeptide complex of 4mg, add the incomplete Freund's adjuvant booster immunization once with the hemocyanin polypeptide complex again after 15 days.Employing is done the titre that ELISA measures antibody in the rabbit anteserum through the titer plate of 15 μ g/ml bovine serum albumin polypeptide complex bag quilts.From the rabbit anteserum of antibody positive, separate total IgG with albumin A-Sepharose.Polypeptide is incorporated on the Sepharose4B post of cyanogen bromide-activated, from total IgG, separates anti-peptide antibody with affinity chromatography.Immuno-precipitation proof antibody purified can combine with human protein synthetic protein L14.22 specifically.
Sequence table
＜110〉Bode Gene Development Co., Ltd., Shanghai
The polynucleotide of＜a 120〉peptide species--human protein synthetic protein L14.22 and this peptide species of coding
<130>0507e08
<160>6
<170>PatentIn?version?3.1
<210>1
<211>1080
<212>DNA
<213>Homo?sapiens
<220>
<221>CDS
<222>(413)..(1024)
<223>
<400>1
gacggttaac?tttgacccaa?agacaacctc?ttctctcccg?cttctctcgc?tgtgaagatg 60
gcgctctcca?gggtgtgctg?ggctcggtcg?gctgtgtggg?gctcggcagt?cacccctgga 120
cattttgtca?cccggaggct?gcaacttggt?cgctctggcc?tggcttgggg?ggcccctcgg 180
tcttcaaagc?ttcacctttc?tccaaaggca?gatgtgaaga?acttgatgtc?ttatgtggta 240
accaagacaa?aagcgattaa?tgggaaatac?catcgtttct?tgggtcgtca?tttcccccgc 300
ttctatatcc?tgtacacaat?cttcatgaaa?gttccgccaa?gacgtcacca?agtgtctttt 360
cctaggtatt?atttccattc?caccttttgc?caactacctg?gtcttcttgc?ta?atg?tac 418
Met?Tyr
1
ctg?ttt?ccc?agg?caa?cta?ctg?atc?agg?cat?ttc?tgg?acc?cca?aaa?caa 466
Leu?Phe?Pro?Arg?Gln?Leu?Leu?Ile?Arg?His?Phe?Trp?Thr?Pro?Lys?Gln
5 10 15
caa?act?gat?ttc?tta?gat?atc?tat?cat?gct?ttc?cgg?aag?cag?tcc?cac 514
Gln?Thr?Asp?Phe?Leu?Asp?Ile?Tyr?His?Ala?Phe?Arg?Lys?Gln?Ser?His
20 25 30
cca?gaa?att?att?agt?tat?tta?gaa?aag?gtc?att?cct?ctc?att?tct?gat 562
Pro?Glu?Ile?Ile?Ser?Tyr?Leu?Glu?Lys?Val?Ile?Pro?Leu?Ile?Ser?Asp
35 40 45 50
gca?gga?ctc?cgg?tgg?cgt?ctg?aca?gat?ctg?tgc?acc?aag?ata?cag?cgt 610
Ala?Gly?Leu?Arg?Trp?Arg?Leu?Thr?Asp?Leu?Cys?Thr?Lys?Ile?Gln?Arg
55 60 65
ggt?acc?cac?cca?gca?ata?cat?gat?atc?ttg?gct?ctg?aga?gag?tgt?ttc 658
Gly?Thr?His?Pro?Ala?Ile?His?Asp?Ile?Leu?Ala?Leu?Arg?Glu?Cys?Phe
70 75 80
tct?aac?cat?cct?ctg?ggc?atg?aac?caa?ctc?cag?gct?ttg?cac?gtg?aaa 706
Ser?Asn?His?Pro?Leu?Gly?Met?Asn?Gln?Leu?Gln?Ala?Leu?His?Val?Lys
85 90 95
gcc?ttg?agc?cgg?gcc?atg?ctt?ctc?aca?tct?tac?ctg?cct?cct?ccc?ttg 754
Ala?Leu?Ser?Arg?Ala?Met?Leu?Leu?Thr?Ser?Tyr?Leu?Pro?Pro?Pro?Leu
100 105 110
ttg?aga?cat?cgt?ttg?aag?act?cat?aca?act?gtg?att?cac?caa?ctg?gac 802
Leu?Arg?His?Arg?Leu?Lys?Thr?His?Thr?Thr?Val?Ile?His?Gln?Leu?Asp
115 120 125 130
aag?gct?ttg?gca?aag?ctg?ggg?att?ggc?cag?ctg?act?gct?cag?gaa?gta 850
Lys?Ala?Leu?Ala?Lys?Leu?Gly?Ile?Gly?Gln?Leu?Thr?Ala?Gln?Glu?Val
135 140 145
aaa?tcg?gct?tgt?tat?ctc?cgt?ggc?ctg?aat?tct?acg?cat?att?ggt?gaa 898
Lys?Ser?Ala?Cys?Tyr?Leu?Arg?Gly?Leu?Asn?Ser?Thr?His?Ile?Gly?Glu
150 155 160
gat?agg?tgt?cga?act?tgg?ctg?gga?gaa?tgg?ctg?cag?att?tcc?tgc?agc 946
Asp?Arg?Cys?Arg?Thr?Trp?Leu?Gly?Glu?Trp?Leu?Gln?Ile?Ser?Cys?Ser
165 170 175
ctg?aaa?gaa?gct?gag?ctg?tct?ctc?ttg?ctg?cac?aac?gtg?gtc?ctg?ctc 994
Leu?Lys?Glu?Ala?Glu?Leu?Ser?Leu?Leu?Leu?His?Asn?Val?Val?Leu?Leu
180 185 190
tcc?acc?aac?tac?ctt?ggg?aca?agg?cgc?tga?atgaaccatg?gagcggatgg 1044
Ser?Thr?Asn?Tyr?Leu?Gly?Thr?Arg?Arg
195 200
cattgtcctg cagtcgtata gtatagcagt gcagga
1080
<210>2
<211>203
<212>PRT
<213>Homo?sapiens
<400>2
Met?Tyr?Leu?Phe?Pro?Arg?Gln?Leu?Leu?Ile?Arg?His?Phe?Trp?Thr?Pro
1 5 10 15
Lys?Gln?Gln?Thr?Asp?Phe?Leu?Asp?Ile?Tyr?His?Ala?Phe?Arg?Lys?Gln
20 25 30
Ser?His?Pro?Glu?Ile?Ile?Ser?Tyr?Leu?Glu?Lys?Val?Ile?Pro?Leu?Ile
35 40 45
Ser?Asp?Ala?Gly?Leu?Arg?Trp?Arg?Leu?Thr?Asp?Leu?Cys?Thr?Lys?Ile
50 55 60
Gln?Arg?Gly?Thr?His?Pro?Ala?Ile?His?Asp?Ile?Leu?Ala?Leu?Arg?Glu
65 70 75 80
Cys?Phe?Ser?Asn?His?Pro?Leu?Gly?Met?Asn?Gln?Leu?Gln?Ala?Leu?His
85 90 95
Val?Lys?Ala?Leu?Ser?Arg?Ala?Met?Leu?Leu?Thr?Ser?Tyr?Leu?Pro?Pro
100 105 110
Pro?Leu?Leu?Arg?His?Arg?Leu?Lys?Thr?His?Thr?Thr?Val?Ile?His?Gln
115 120 125
Leu?Asp?Lys?Ala?Leu?Ala?Lys?Leu?Gly?Ile?Gly?Gln?Leu?Thr?Ala?Gln
130 135 140
Glu?Val?Lys?Ser?Ala?Cys?Tyr?Leu?Arg?Gly?Leu?Asn?Ser?Thr?His?Ile
145 150 155 160
Gly?Glu?Asp?Arg?Cys?Arg?Thr?Trp?Leu?Gly?Glu?Trp?Leu?Gln?Ile?Ser
165 170 175
Cys?Ser?Leu?Lys?Glu?Ala?Glu?Leu?Ser?Leu?Leu?Leu?His?Asn?Val?Val
180 185 190
Leu?Leu?Ser?Thr?Asn?Tyr?Leu?Gly?Thr?Arg?Arg
195 200
<210>3
<211>24
<212>DNA
<213>Homo?sapiens
<400>3
gacggttaac tttgacccaa agac
24
<210>4
<211>24
<212>DNA
<213>Homo?sapiens
<400>4
gctttcaagc agtctttact tggg
24
<210>5
<211>34
<212>DNA
<213>Homo?sapiens
<400>5
ccccatatga tgtacctgtt tcccaggcaa ctac
34
<210>6
<211>34
<212>DNA
<213>Homo?sapiens
<400>6
catggatcct cagcgccttg tcccaaggta gttg
34
Claims (10)
1, a kind of isolated polypeptide-human protein synthetic protein L14.22 is characterized in that it includes: the polypeptide of the aminoacid sequence shown in＜210〉2 or the active fragments of its polypeptide, analogue or derivative.
2, polypeptide as claimed in claim 1, the aminoacid sequence that it is characterized in that described polypeptide, analogue or derivative has the homogeny with the aminoacid sequence at least 95% shown in＜210〉2.
3, polypeptide as claimed in claim 2 is characterized in that it comprises and has＜polypeptide of the aminoacid sequence shown in 210〉2.
4, a kind of isolating polynucleotide, it is characterized in that described polynucleotide comprise be selected from down the group in a kind of:
(a) coding have＜210〉2 shown in the polynucleotide of the polypeptide of aminoacid sequence or its fragment, analogue, derivative;
(b) with polynucleotide (a) complementary polynucleotide; Or
(c) with (a) or the polynucleotide of at least 70% homogeny (b) are arranged.
5, polynucleotide as claimed in claim 4, it is characterized in that described polynucleotide comprise coding and have＜210〉2 shown in the polynucleotide of aminoacid sequence.
6, polynucleotide as claimed in claim 4, it is characterized in that the sequence of described polynucleotide includes＜210〉1 in the 413-1024 position sequence or＜210〉1 in the sequence of 1-2002 position.
7, a kind of recombinant vectors that contains exogenous polynucleotide is characterized in that it is the recombinant vectors that is formed by the described polynucleotide of arbitrary claim among the claim 4-6 and plasmid, virus or vehicle expression vector establishment.
8, a kind of genetically engineered host cell that contains exogenous polynucleotide is characterized in that it is to be selected from following a kind of host cell:
(a) host cell that transforms or transduce with the described recombinant vectors of claim 7; Or
(b) host cell that transforms or transduce with the described polynucleotide of the arbitrary claim among the claim 4-6.
9, a kind of preparation method with the active polypeptide of human protein synthetic protein L14.22 is characterized in that described method comprises:
(a) under expressing human protein synthetic protein L14.22 condition, cultivate the described through engineering approaches host cell of claim 8;
(b) from culture, isolate and have the active polypeptide of human protein synthetic protein L14.22.
10, a kind of can with polypeptide bonded antibody, it is characterized in that described antibody be can with human protein synthetic protein L14.22 specificity bonded antibody.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNA021377278A CN1493591A (en) | 2002-10-30 | 2002-10-30 | Polypeptide-human protein synthetic protein L14, 22 and nucleotide for coding said polypeptide |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNA021377278A CN1493591A (en) | 2002-10-30 | 2002-10-30 | Polypeptide-human protein synthetic protein L14, 22 and nucleotide for coding said polypeptide |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN1493591A true CN1493591A (en) | 2004-05-05 |
Family
ID=34231677
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNA021377278A Pending CN1493591A (en) | 2002-10-30 | 2002-10-30 | Polypeptide-human protein synthetic protein L14, 22 and nucleotide for coding said polypeptide |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN1493591A (en) |
-
2002
- 2002-10-30 CN CNA021377278A patent/CN1493591A/en active Pending
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