CN1318550A - O-sialogycoproteinase-like protein and polynucleotide sequence for encoding it - Google Patents

O-sialogycoproteinase-like protein and polynucleotide sequence for encoding it Download PDF

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CN1318550A
CN1318550A CN 00106834 CN00106834A CN1318550A CN 1318550 A CN1318550 A CN 1318550A CN 00106834 CN00106834 CN 00106834 CN 00106834 A CN00106834 A CN 00106834A CN 1318550 A CN1318550 A CN 1318550A
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polypeptide
sequence
polynucleotide
osgplp
dna
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毛裕民
谢毅
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SHANGHAI SHENGYUAN GENE DEVELOPMENT Co Ltd
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SHANGHAI SHENGYUAN GENE DEVELOPMENT Co Ltd
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Abstract

The present invention discloses the polynucleotides sequence of separated human O-sialogycoproteinase-like protein gene and its encoded polypeptide as well as the method of preparing the polypeptide. The present invention also discloses the method of applying the polypeptide in the diagnosis, preventing and/or treatment of related diseases. The present invention also discloses the method of utilizing the polypeptide of the present invention in screening its agaonist, excitomotor and inhibitor and preparing antibody against the polypeptide, the use of the polynucleotides sequence, polypeptide, agonist, excitomotor, inhibitor and antibody in treating disease related to the abnomral gene and in preparing the medicine composite for the treatment.

Description

A kind of O-sialoglycoprotein enzyme sample albumen and its polynucleotide sequence of encoding
The invention discloses the polynucleotide sequence and the encoded polypeptides thereof of isolating O-sialoglycoprotein enzyme sample albumen (being designated hereinafter simply as OSGPLP) gene, and the method for preparing this peptide species.The present invention also discloses this peptide species has been used for multiple disease, as the methods of treatment of malignant tumour, hemopathy, immunological disease and all kinds of inflammation etc.In addition, the invention also discloses, detect and the nucleic acid of this gene and the diagnostic method of the unusual diseases associated of coded polypeptide thereof by sudden change in the nucleotide sequence of differentiating OSGPLP and the change of OSGPLP level.The invention also discloses and utilize polypeptide of the present invention to screen antagonist, the agonist of this polypeptide, the method for inhibition, and preparation is at the method for the antibody of polypeptide of the present invention, also discloses the purposes of the polynucleotide sequence that utilizes gene of the present invention and polypeptide and antagonist, agonist, inhibition and Antybody therapy and this gene unconventionality diseases associated and has been used to prepare the purposes of the pharmaceutical composition that is used for above-mentioned treatment.
O-sialoglycoprotein enzyme is considered to a specific specificity protein hydrolysate, and Serine, threonine residues are connected with the protein of sialic acid polysaccharide on its hydrolyzable peptide chain.People such as K.M.Abdullah obtain the gcp gene first from pasteurella haemolytica serotype A 1, it translates albumen called after glucoproteinase or O-sialoglycoprotein endopeptidase (E.C.3.4.24.57).(people such as Alan Mellors, 1995, Enzymology method (Methods.Enzymol.) 248; 728-740).O-sialoglycoprotein enzyme is a kind of metalloprotease.The EDTA of high density loses activity it, and after dialysis, it is active that enzyme recovers again.Infer metal ion can combine closely with enzyme (people such as K.M.Abdullah, 1992, infect and immunity (Infect.Immun.), 60:56).
O-sialoglycoprotein endopeptidase effect substrate generally is the glycoprotein of cell surface, as HRBC glycophorin A, CD34 (marrow raw blood stem cell surface antigen), CD43 (leukosialin), CD44 (hyaluronic acid acceptor), CD45 (white corpuscle common antigen), palatelet-selectin (P-selectin) counter receptor, interleukin-17 receptor, epitectin (human tumor cells surface antigen) etc., this class substrate extracellular domain serine/threonine content about 30% usually.This type of glycoprotein had both contained the O-polysaccharide, contain the N-polysaccharide again, but the only single-minded hydrolysis O-of O-sialoglycoprotein enzyme polysaccharide (that is: sialic acid) albumen (people such as Sutherland DR, on March 1st, 1992, Journal of Immunology (J.Immunol.), 148 (5): 1458-64).Clostridium perfringens neuraminidase is removed the sialic acid of glycophorin A, then destroys the susceptibility of glycoprotein to O-sialoglycoprotein enzyme.Infer that the contiguous sialic acid residues of this enzyme require is in conjunction with the work of finishing the range of hydrolysed peptides chain backbone.(people such as K.M.Abdullah, 1992, infect and immunity, 60,56).
O-sialoglycoprotein enzyme plays an important role in regulating body critical functions such as cell fission, fetal development, immune response as mentioned above, believes to relate to a large amount of these proteinoid in this regulate process.Thereby need to identify the O-sialoglycoprotein enzyme of a greater variety of these processes of participation in this area always, particularly identify the aminoacid sequence of these O-sialoglycoprotein enzymes.The invention provides a kind of new O-sialoglycoprotein enzyme sample albumen (being designated hereinafter simply as OSGPLP) and encoding gene thereof, be providing the foundation of determining further that clear and definite this proteinoid acts 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.Can be used for the diagnosis and the treatment of its relative disease.
Purpose of the present invention just provides a kind of new O-sialoglycoprotein enzyme sample albumen and encodes its polynucleotide.Polypeptide of the present invention has the feature structure territory of O-sialoglycoprotein enzyme sample protein gene, thereby infers that OSGPLP of the present invention is a kind of this new proteinoid.
The present invention relates to a kind of isolated polypeptide, it comprises: polypeptide or its examples of conservative variations, bioactive fragment or derivative with SEQ ID No.2 aminoacid sequence.
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 the polynucleotide of the polypeptide of SEQ ID No.2 aminoacid sequence;
(b) with polynucleotide (a) complementary polynucleotide;
(c) with (a) or polynucleotide sequence (b) have the polynucleotide of at least 70% homogeny.
Especially, described polynucleotide sequence is selected from: the sequence that (a) has 110-1354 position among the SEQ ID NO:1; (b) has the sequence of 1-2058 position among the SEQ ID NO:1
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.
The invention still further relates to a kind of simulation, activation, antagonism of screening or suppress the method for the compound of polypeptide active of the present invention, it comprises and utilizes polypeptide of the present invention.The invention still further relates to the compound that obtains with this method.
The invention still further relates to a kind of vitro detection and express the relevant disease or the method for disease susceptibility with this O-sialoglycoprotein enzyme sample abnormal protein, comprise the sudden change in polypeptide described in the detection of biological sample or its coded polynucleotide sequence, perhaps the amount or the biological activity of polypeptide of the present invention in the detection of biological sample.
The present invention also relates to a kind of pharmaceutical composition, it contains polypeptide of the present invention or its stand-in, activator, antagonist or inhibitor and pharmaceutically acceptable carrier.
The invention still further relates to polypeptide of the present invention and/or polynucleotide and be used for the treatment of malignant tumour, hemopathy, immunological disease or various inflammation or other because the purposes in the medicine of the caused disease of OSGPLP abnormal expression in preparation.
The antagonist or the antisense polynucleotides that the invention still further relates to polypeptide of the present invention are used for the treatment of malignant tumour, hemopathy or immunological disease and various inflammation or other because the purposes in the medicines such as disease that the OSGPLP abnormal expression causes in preparation.
Fig. 1 is the amino acid sequence homology comparison diagram of OSGPLP of the present invention and possible O-sialoglycoprotein endopeptidase (gcp) [Rickettsia prowazekii].Top sequence (Query) is OSGPLP, and below sequence (Sbjct) is possible O-sialoglycoprotein endopeptidase (gcp) [Rickettsia prowazekii].Same amino acid represents with monocase amino acid that between two sequences similar amino acid is represented with "+".Comparison length is 387 amino acid, must be divided into 457 (160.9 bits), expects to be 6.9e-54, adds and P (2)=6.9e-54; Homogeny=106/274 (38%), similarity=152/274 (55%)
Fig. 2 is the polyacrylamide gel electrophoresis figure (SDS-PAGE) of isolating OSGPLP.Wherein swimming lane 1 is a protein molecular weight standard, and swimming lane 2,3 is for containing the sample of target protein, and swimming lane 4 is purified target protein (arrow indication), and the molecular weight size is 46kDa.
The present invention above-mentioned with other the aspect for a person skilled in the art, see it is very clearly from this paper the following detailed description.
The following term of using in this specification sheets and claims has following implication unless stated otherwise:
" nucleotide sequence " is meant oligonucleotide, Nucleotide or polynucleotide and fragment or part, also can refer to genome or synthetic DNA or RNA, and they can be strand or two strands, represent sense strand or antisense strand.Similarly, term " aminoacid sequence " is meant oligopeptides, peptide, polypeptide or protein sequence and fragment or part.When " aminoacid sequence " among the present invention related to a kind of aminoacid sequence of naturally occurring protein molecule, this " polypeptide " or " protein " did not mean that aminoacid sequence are restricted to the complete natural amino acid relevant with described protein molecule.
Protein or polynucleotide " variant " are meant a kind of polynucleotide sequence that has the aminoacid sequence of one or more amino acid or Nucleotide change or encode it.Described change can comprise disappearance, insertion or the replacement of amino acid in aminoacid sequence or the nucleotide sequence or Nucleotide.Variant can have " conservative property " and change, and wherein the amino acid of Ti Huaning has structure or the chemical property similar with original acid, as replacing Isoleucine with leucine.Variant also can have non-conservation and change, as replacing glycine with tryptophane.
" disappearance " is meant the disappearance of in aminoacid sequence or nucleotide sequence one or more amino acid or Nucleotide.
" insertion " or " interpolation " is meant that the change in aminoacid sequence or nucleotide sequence causes comparing the increase of one or more amino acid or Nucleotide with naturally occurring molecule.
" replacement " is meant by different amino acid or Nucleotide and replaces one or more amino acid or Nucleotide.
" biological activity " is meant the protein of structure, regulation and control or biochemical function with natural molecule.Similarly, term " immunologic competence " be meant natural, reorganization or synthetic protein and fragment thereof in suitable animal or cell, induce specific immune response and with specific antibody bonded ability.
" agonist " is meant when combining with OSGPLP, thereby a kind of this protein that causes changes the molecule of regulating this protein active.Agonist can comprise protein, nucleic acid, carbohydrate or any other can be in conjunction with the molecule of OSGPLP.
" antagonist " or " inhibition " be meant when combining with OSGPLP, a kind ofly seals or regulate the biologic activity of OSGPLP or the molecule of immunologic competence.Antagonist and inhibition can comprise protein, nucleic acid, carbohydrate or any other can be in conjunction with the molecule of OSGPLP.
" adjusting " is meant that the function of OSGPLP changes, and comprises the change of any other biological property, function or the immune property of the change of the rising of protein active or reduction, binding characteristic and OSGPLP.
" pure basically " is meant and is substantially free of natural relative other albumen, lipid, carbohydrate or other material.Those skilled in the art can use the purified technology of protein purifying OSGPLP of standard.Basically pure OSGPLP can produce single master tape on the irreducibility polyacrylamide gel.The purity available amino end acid sequence of OSGPLP polypeptide is analyzed.
" complementary " or " complementation " is meant under salt concn that allows and temperature condition by the natural combination of the polynucleotide of base pairing.For example, sequence " C-T-GA " can combine with complementary sequence " G-A-C-T ".Complementation between two single chain molecules can be part or whole.Complementary degree between the nucleic acid chains has a significant effect for efficient of hybridizing between the nucleic acid chains and intensity.
" homology " is meant the complementary degree, can be portion homologous or complete homology." portion homologous " is meant a kind of part complementary sequence, and it can partly suppress the hybridization of complete complementary sequence and target nucleic acid at least.The inhibition of this hybridization can detect by hybridizing (Southern trace or Northern trace etc.) under the condition that reduces in the severity degree.Basically homologous sequence or hybridization probe can compete and suppress complete homologous sequence and target sequence the condition that reduces of severity degree under combine.This does not mean the conditions permit non-specific binding that the severity degree reduces because the conditional request two sequences that the severity degree reduces mutual be combined into specificity or selectivity interacts.
" homogeny percentage " be meant two or more amino acid or nucleotide sequence relatively in the same or analogous percentage of sequence.The available electron method is measured the homogeny percentage, as by the MEGALIGN program (the Lasergene software package, DNASTAR, Inc., MadisonWis.).The MEGALIGN program can according to diverse ways such as Cluster method relatively two or more sequences (Higgins, D.G. and P.M.Sharp (1988), gene, 73:237-244).The Cluster method is organized the series arrangement cluster by checking the distance between all pairings with each.Then with each bunch with in pairs or become set of dispense.Homogeny percentage between two aminoacid sequences such as sequence A and the sequence B calculates by following formula:
Figure A0010683400091
Also can be by the Cluster method or with the homogeny percentage (Hein J., (1990) Enzymology method (Methods inenzymology) 183:625-645) between known method in this area such as the Jotun Hein mensuration nucleotide sequence.
" similarity " is meant the degree that the identical or conservative property of corresponding position amino-acid residue when arranging contrast between the aminoacid sequence replaces.For example be used for amino acid that conservative property replaces, electronegative amino acid can comprise aspartic acid and L-glutamic acid; Positively charged amino acid can comprise Methionin and arginine; Having uncharged head group has similar hydrophilic amino acid can comprise leucine, Isoleucine and Xie Ansuan; Glycine and L-Ala; L-asparagine and glutamine; Serine and Threonine; Phenylalanine and tyrosine.
" antisense " is meant and specific DNA or RNA sequence complementary nucleotide sequence." antisense strand " is meant and " sense strand " complementary nucleic acid chains.
" derivative " is meant OSGPLP or encodes its chemical modification object of nucleic acid.This chemical modification object can be with alkyl, acyl group or the amino hydrogen atom of replacing.The nucleic acid derivative codified keeps the polypeptide of the main biological characteristics of natural molecule.
" antibody " is meant complete antibody molecule and fragment thereof, as Fa, F (ab ') 2And Fv, its energy specificity is in conjunction with the antigenic determinant of OSGPLP.
" isolating " speech refers to material is shifted out among its original environment (for example, if spontaneous its natural surroundings that just refers to).Such as it is exactly not to be separated that spontaneous polynucleotide or polypeptide are present in the Live Animals, but same polynucleotide or polypeptide with some or all in natural system with it the material of coexistence separately be exactly isolating.Such polynucleotide may be the parts of a certain carrier, the part that also possible such polynucleotide or polypeptide are a certain composition.Since carrier or composition are not the compositions of its natural surroundings, they remain isolating.
One aspect of the present invention provides a kind of new people O-sialoglycoprotein enzyme sample albumen, and biologically active fragment, analogue and derivative.Another aspect of the present invention provides the isolated nucleic acid molecule of these polypeptide of encoding, and comprises mRNA, DNA, cDNA and genomic dna, and the fragment of biologically active, analogue and derivative.The probe that nucleic acid is provided on the one hand more of the present invention, it comprises the nucleic acid molecule of sufficient length and carries out the sequence of specific hybrid with the OSGPLP gene order.
According to an aspect of of the present present invention, it provides a kind of isolating polynucleotide, and these nucleotide codings have the polypeptide of the aminoacid sequence of inferring shown in the SEQ ID No.2.
The polynucleotide of coding OSGPLP can separate from the cDNA library of many adults and fetus, as people's tire brain cDNA library.Polynucleotide sequence total length shown in the SEQ ID No.1 is 2058 bases, and its open reading frame (110-1354 among the SEQ ID NO:1) has the polypeptide of 414 amino-acid residues of coding.Find relatively that according to amino acid sequence homologous this polypeptide and possible O-sialoglycoprotein endopeptidase have 106/274 (38%) homogeny, infer that this novel polypeptide has and the possible similar function of O-sialoglycoprotein endopeptidase.
Polynucleotide of the present invention can RNA or the form of DNA exist, wherein DNA comprises cDNA, genomic dna and synthetic DNA.DNA can be two strands or strand, and strand also can be sense strand or antisense strand.The polynucleotide sequence of coded polypeptide can be identical with the polynucleotide sequence shown in the SEQ IDNo.1, perhaps can be one because the redundancy of genetic code or degeneracy and different polynucleotide sequences, but its and the SEQ ID No.1 identical mature polypeptide of encoding.
The polynucleotide of the polypeptide of coding SEQ ID No.2 can comprise: the only polynucleotide sequence of encoding mature polypeptide (as 110-1354 position polynucleotide among the SEQ ID No.1), the polynucleotide sequence that comprises the encoding mature polypeptide and optional other encoding sequence or the polynucleotide sequence (as 1-2058 position polynucleotide among the SEQ ID No.1) of non-coding sequence (for example the polynucleotide sequence 5 ' end of intron or encoding mature polypeptide and/or the non-coding sequence of 3 ' end).
The invention further relates to the various variants of polynucleotide described above, their codings contain fragment, analogue and the derivative of the aminoacid sequence polypeptide of inferring shown in the SEQ ID No.2.These polynucleotide variants can be the polynucleotide variants that naturally occurring allele variant or non-natural exist.
The polynucleotide of code book invention polypeptide also may merge in same frame mutually with the specific markers sequence, and flag sequence can help the purifying of polypeptide of the present invention.Flag sequence can be six polyhistidine tags of pQE carrier when using host bacterium, be beneficial to merge the purifying of markd mature polypeptide, perhaps when using mammals host (as the fibroblastic COS-7 clone of monkey kidney), flag sequence can be a kind of hemagglutinin (HA) mark.In addition, the polynucleotide sequence that comprises code book invention polypeptide also can comprise homology or allogenic signal specific peptide sequence, is secreted into outside prokaryotic cell prokaryocyte or the eukaryotic cell membrane to help target protein matter.Those of ordinary skills know, and above-mentioned flag sequence and signal peptide sequence also can be added on the carrier that is used to express polypeptide of the present invention by recombination method or chemical method.
Polynucleotide sequence of the present invention also comprises the fragment of full-length cDNA, among the SEQ IDNo.2 that for example encodes at least 20, and preferably at least 30, more preferably at least 50, best at least 80 amino acid whose polynucleotide passages.These fragments for example have shown in the SEQID No.1 in the sequence at least 10 of successive, preferred at least 20 Nucleotide, preferred at least 50 Nucleotide, particularly at least 60,90,150 or 240 Nucleotide.
The invention further relates to can with the polynucleotide of above-mentioned sequence hybridization, have 70% at least between these two sequences, more preferably at least 80%, preferably at least 90%, more preferably at least 95% homology.The present invention be more particularly directed under stringent condition can with the polynucleotide of above-mentioned multi-nucleotide hybrid.Terminology used here " stringent condition " means between two sequences have 95%, and preferably at least 97% homology could be hybridized.In an embodiment preferred, kept substantially and identical biological function or the activity of polypeptide shown in the SEQ ID No.2 with the polypeptide of the polynucleotide encoding of above-mentioned polynucleotide complementary strand hybridization.
In addition, the present invention relates to can with the polynucleotide of multi-nucleotide hybrid of the present invention, it contains 20 bases at least, preferred at least 30 bases, more preferably at least 50 bases and have homology described above, it can keep or retentive activity not.For example, such polynucleotide can be used as the probe of the similar sequences that detects polynucleotide shown in the SEQ ID No.1 or other source; And for example, it can be used for the recovery of polynucleotide of the present invention or as a kind of diagnostic probe or PCR primer.
Dna sequence dna of the present invention can obtain with several different methods.For example, with hybridization technique DNA isolation 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 homology polynucleotide sequence and 2) antibody screening of expression library to be to detect the dna fragmentation of the clone with common structure feature.
The specific DNA fragment sequence of coding OSGPLP 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 required polypeptide.
The standard method that separates interested cDNA is a separating mRNA and carry out reverse transcription from the donorcells of this gene of high expression level, 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 the known method of those skilled in the art (people such as Sambrook, molecular cloning laboratory manual (Molecular Cloning, 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 polynucleotide sequence of the present invention from these cDNA libraries.These methods include but not limited to: (1) DNA-DNA or DNA-RNA hybridization; (2) function of marker gene occurs or forfeiture; (3) level of the transcript of mensuration OSGPLP; (4) applied immunology technology or mensuration biologic activity detect the protein product of genetic expression.Aforesaid method can use separately, but also several different methods combined utilization.
In (1) kind method, hybridizing used probe can have homogeny with any part of polynucleotide of the present invention, and its length is 15 Nucleotide at least, preferably 20-30 Nucleotide, being more preferably 50-60 Nucleotide, most preferably is 100 more than the Nucleotide.Probe used herein is the dna sequence dna of chemosynthesis on the basis of gene DNA sequence information of the present invention normally.Gene of the present invention itself or fragment certainly are used as probe.Dna probe can be used radio isotope, fluorescein or enzyme marks such as (as alkaline phosphatases).In (4) the kind method, the protein product that detects OSGPLP genetic expression can be with immunological technique such as Western trace, radioimmunoprecipitation, enzyme-linked immunosorbent assay (ELISA) etc.
Because the application provides the full length cDNA sequence of OSGPLP, (Saiki waits the people to the method for application round pcr DNA amplification/RNA, science (Science) 1985; 230:1350-1354) be preferred for obtaining 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), can suitably select according to sequence information of the present invention disclosed herein at primer used aspect the above-mentioned PCR, 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 available ordinary method of the mensuration of the nucleotide sequence of various dna fragmentations such as dideoxy chain termination (people such as Sanger, institute of NAS newspaper, 1977,74:5463-5467).This class nucleotide sequencing is available commercial sequencing kit etc. also.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, to be spliced into the cDNA sequence of total length.
The all or part of of polynucleotide sequence of the present invention also can be by the known chemical process in this area synthetic (Caruthers, people such as M.H., (1980) Nucl.Acids Res.Symp.Ser.215-223; Horn, people such as T., (1980) Nucl.Acid Res.Symp.Ser.225-232).
The invention further relates to polypeptide and active fragments, analogue and derivative with putative amino acid sequence shown in the SEQ ID No.2.The polypeptide of putative amino acid sequence shown in the SEQ ID No.2 is a polypeptide that contains 414 amino-acid residues.
" fragment " of polypeptide shown in the SEQ ID No.2, " derivative " and " analogue " refer to keep substantially the biological function of this polypeptide or the precursor of active polypeptide or non-activity.Thus, polypeptide of the present invention has comprised forms such as its preceding former albumen, preceding albumen and proteinogen, and it can be activated through processing back (as proteolysis or modification), produces an activated mature polypeptide.
Polypeptide of the present invention can be recombinant polypeptide, naturally occurring polypeptide or synthetic polypeptide, is preferably recombinant polypeptide.Fragment, derivative and the analogue of the polypeptide shown in the SEQ ID No.2 can be: (ⅰ) one or more amino-acid residues are replaced the polypeptide of (preferably conservative amino acid residue) by conservative property or non-conservation amino-acid residue, and the amino-acid residue yes or no of replacement is by the coded amino acid of genetic code.For example, can obtain silent mutation body or the function equivalent of OSGPLP by insertion, replacement and/or the deletion of amino-acid residue.Can replace based on carrying out conservative amino acid in the similarity of polarity, electric charge, solvability, hydrophobicity, wetting ability and/or aspect such as amphipathic between the amino-acid residue, as long as keep the activity of OSGPLP; Or (ⅱ) one or more amino-acid residues have the polypeptide of substituted radical; Or (ⅲ) mature polypeptide and other functional compound, the polypeptide that merges as the compound (for example polyoxyethylene glycol) that improves the polypeptide half life; Or (ⅳ) polypeptide that merges mutually of mature polypeptide and other aminoacid sequence, wherein said other aminoacid sequence comprises such as aminoacid sequence that helps the purifying maturation protein or proteinogen sequence etc.These help the structural domain of purifying to include but not limited to: metal-chelate is closed peptide, as is used for the Histidine-tryptophane module of purifying on immobilization metal; Be used for the albumin A structural domain of purifying on the immobilization immunoglobulin (Ig) and be used for FLAGS extension/affinity purification system structural domain (IMMUNEX company, Seattle, Wash).The fracture joint sequence that is specific to factor XA or enteropeptidase also can be used for helping the purifying of target protein matter (Porath, people such as J. (1992), Prot.Exp.Purif.3:263-281).From these disclosures, in the ken that should be in those skilled in the art of such fragment, derivative and analogue.
Polypeptide of the present invention comprises the polypeptide (referring in particular to mature polypeptide) shown in the SEQ ID No.2, also comprise the polypeptide that has 70% similarity (preferably 70% homogeny) with SEQ ID No.2 polypeptide at least, the polypeptide that preferably has 90% similarity (preferably 90% homogeny) at least, the polypeptide that more preferably has 95% similarity (preferably 95% homogeny) at least, the some parts that also comprises these polypeptide, these polypeptide portions contain 30 amino acid, preferred at least 50 amino acid at least usually.
Polypeptide of the present invention, its examples of conservative variations and bioactive fragment and derivative can prepare with conventional peptide synthetic method, for example synthetic (Merrifield J. (1963), American Chemical Society's magazine (J.Am.Chem.Soc.) 85:2149-2154 of solid-phase peptide; Roberge, people such as J.Y., (1995) science, 269:202-204).Protein synthesis can be finished by hand, also can utilize automatic peptide synthesizer such as Applied Biosystems 431A peptide synthesizer to carry out (Perkin Elmer).Polypeptide of the present invention also can obtain through separation and purification from natural biologic material, but preferably utilizes polynucleotide provided by the invention to prepare with recombinant DNA technology.According to host's difference used in the recombinant method for production, the polypeptide among the present invention may be by glycosylation or not by glycosylation.This polypeptide also may have initial methionine residues.
According to common recombinant DNA technology, utilize polynucleotide sequence of the present invention can express or prepare OSGPLP polypeptide (science, 1984 of reorganization; 224:1431).The present invention thereby relate to the method for preparing OSGPLP polypeptide of the present invention generally comprises following steps:
(1) transforms proper host cell with the encode polynucleotide (or variant) of OSGPLP or the recombinant expression vector that contains these polynucleotide of the present invention;
(2) in suitable medium and under the suitable culture condition, cultivate host cell;
(3) separation, purifying target protein matter from substratum or cell.
The present invention also relates to comprise polynucleotide of the present invention recombinant vectors, have the genetically engineered host cell of recombinant vectors of the present invention and prepare the method for polypeptide of the present invention by recombinant technology.
Polynucleotide of the present invention can be used for producing polypeptide through recombinant technology.For example, these polynucleotide may reside in and are selected from the multiple arbitrary carrier that is used for the expression vector of express polypeptide, these carriers comprise chromosomal, achromosomal and synthetic dna sequence dna, for example, the derivative of SV40, bacterial plasmid, phage DNA, yeast plasmid, be derived from plasmid and phage DNA bonded carrier, viral DNA, baculovirus, vaccinia virus, adenovirus, fowlpox virus and Pseudorabies virus include but not limited to pQE series (Qiagen), pBS, pD10, phagescript, psiX174, pBluescript SK, pBSKS, pNH series (Stratagene), pTRC99a, pKK223-3, pDR540, pRIT5 (Pharmacia); PWLNEO, pSV2CAT, pOG44, pXT1, pSG (Stratagene), pSVK3, pBPV, pMSG, pSVL (Pharmacia).But, so long as can duplicate in the host and survive, other plasmid or carrier also can be used.
The present invention also comprises the recombinant precursor that contains polynucleotide of the present invention.This construct comprises carrier, as above-mentioned plasmid or virus vector, wherein can insert polynucleotide sequence of the present invention forward or backwards.Also comprise the adjusting sequence in the construct, for example, be connected to the promotor (comprising composing type and inducible promoter) on the polynucleotide sequence of the present invention effectively, mediate transcribing of downstream configurations sequence.Suitable promotor includes but not limited to, the PL promotor of lambda particles phage, baculovirus polyhedrin body protein promotor; The bacterium promotor as; LacI, LacZ, T3, T7, gpt, λ PR, PL and trp; Eukaryotic promoter is as: CMV immediate early promoter, HSV thymidine kinase promoter, early stage and late period SV40 promotor, retroviral LTR and mouse metallothionein(MT) I promotor; Also comprise derived from the promotor in the vegetable cell genome, as heat shock protein(HSP), RUBISCO promotor.
Expression vector also comprises needed ribosome bind site of translation initiation and transcription terminator, and it can also have the proper sequence that strengthens expression, as enhanser.Enhanser is the cis acting factor of DNA, and about 10-300bp is arranged usually, acts on promotor, improves transcribing of it.For example, be positioned at the enhanser at replication orgin rear side 100-270bp place among the SV40, the sub-enhanser of cytomegalovirus early promoter, the polyoma enhanser that is positioned at the replication orgin rear side and adenovirus enhanser.In addition, expression vector preferably also comprises one or more selected genes, resistant gene and/or the marker gene that phenotypic characteristic can be provided, so that the screening of transformed host cell.Selected gene utilizes trpB, the hisD (Hartman of indoles or histidinol as helping cell, S.C. and institute of R.C.Mulligan (1988) NAS report 85:8047-51), the liver simplexvirus thymidine kinase (Wigler that is used for tk-or aprt-cell, M. wait people (1977) cell, 11:223-32) and adenine phosphoribosyltransferase (Lowy, I. wait people (1980) cell, 22:817-23); Resistant gene is as giving the Tetrahydrofolate dehydrogenase DHFR (Wigler of methotrexate resistance, people such as M (1989), institute of NAS newspaper, 77:3567-70) or give the npt (Colbere-Garapin of Xin Meisu and G418 resistance, F. wait people (1981) molecular biology magazine, 150:1-14), and tsiklomitsin or ampicillin resistance gene.The mammals expression vector generally comprises replication orgin, suitable promotor, enhanser and any essential ribosome bind site, polyadenous glycosidation site, splicing donor and acceptor site, transcription termination sequence and 5 ' flank non-transcribed sequence.The dna sequence dna and the polyadenous glycosidation site that are derived from SV40 splicing sequence can be used for providing needed non-transcribed genetic elements.In addition, the carrier that comprises the nucleotide sequence of code book invention polypeptide also can comprise homology or allogenic signal specific peptide sequence, is secreted into outside prokaryotic cell prokaryocyte or the eukaryotic cell membrane to help target protein matter.Those of ordinary skills know, and flag sequence that contains in above-mentioned expression vector and the construct and signal peptide sequence also can be added on the polynucleotide of code book invention polypeptide by recombination method or chemical method.
Suitable carrier and promotor to be chosen as those of ordinary skills known.The effective expression carrier that bacterium is suitable for can make up like this: the structural DNA sequence of the target protein of will encoding is inserted in the steerable reading frame that has function in company with suitable translation initiation and termination signal.Those of ordinary skills are known to be used to make up and to contain nucleotide sequence of the present invention and suitable transcribing and the method for translational control element.These methods comprise genetic recombination techniques (Sambrook, J. (1989), " molecular cloning, laboratory manual ", Cold Spring Harbor Press in extracorporeal recombinant DNA technology, synthetic technology and the body; Plainview, N.Y.; Ausubel, F.M. (1989) modern molecular biology method (Current Protocols in MolecularBiology), John Wiley ﹠amp; Sons, N.Y.).
Comprise above-mentioned suitable dna sequence dna, suitable promotor or the carrier of control sequence and can be used to transform appropriate host, allow this albumen of host expresses.
Those skilled in the art know, and the expression vector that dna sequence dna inserted according to the present invention or the kind of construct and characteristic select appropriate host to express target protein matter.The host who is suitable for expressing polypeptide of the present invention includes but not limited to: prokaryotic hosts, such as intestinal bacteria, bacillus, streptomyces etc.; Eucaryon host, such as: yeast belong, Aspergillus, insect cell, such as fruit bat S2 and fall army worm Sf9; Zooblast can be expressed the clone of compatible carrier, for example C127,3T3, CHO, HeLa, BHK, Bowes melanoma cells as CHO, COS (monkey kidney fibroblast, Gluzman, cell, 23:175,1981) and other; Vegetable cell and adenovirus or the like.The culture systems of various mammalian cells also can be used for express recombinant protein.From these instruction, the selection of suitable host should be in those skilled in the art's ken.
Having aforesaid carrier or the construct that contains nucleotide sequence of the present invention can import in the proper host cell to produce recombinant products by traditional method.The method that construct is imported above-mentioned host cell is known for those skilled in the art, include but not limited to: transfection, electroporation, microinjection, particle bombardment method or the particle gun method (Sambrook of the conversion of calcium chloride mediation, calcium phosphate transfection, the mediation of DEAE-dextran, J. (1989), " molecular cloning, laboratory manual ", Cold Spring Harbor Press; Plainview, N.Y.; Ausubel, the modern molecular biosciences method of F.M. (1989), John Wiley ﹠amp; Sons, N.Y.; Hobbs, people such as S., McGraw Hill science and technology yearbook (1992), McGraw Hill, N.Y.191-196; Engelhard, people such as E.K., institute of NAS newspaper, 91:3224-3227; Logan, people such as J., institute of NAS newspaper, 81:3655-3659).
In suitable culture condition and substratum, cultivate through host transformed bacterial strain or cell, it is grown into after the appropriate cell density, induce selected promotor with appropriate means (for example temperature transition or pharmaceutical chemicals are induced), and cell is cultivated for some time again.At different host strains or cell select and the corresponding culture condition of character of expressed target protein matter and substratum within those skilled in the art's ken.
Under suitable promotor control, can in cells of mamma animals, yeast, bacterium or other cell, express maturation protein.Utilization also can produce this protein (Sambrook, J. (1989), " molecular cloning, laboratory manual ", the 18th chapter the 4th joint, Cold Spring Harbor Press with the cell free translation system by DNA construct derived RNA of the present invention; Plainview, N.Y.).
Usually with centrifugation method harvested cell or nutrient solution.The situation in the born of the same parents is stayed in quality guarantee for target protein, general available any physics easily, chemical process or enzyme process, comprise freeze-thaw cycle, ultrasonic wave, Mechanical Crushing, or use cell lytic agent or specific enzyme smudge cells, crude extract is kept to be further purified.For be secreted into the outer situation of born of the same parents for target protein matter, can directly reclaim culture supernatant.These methods all are well-known to those having ordinary skill in the art.
Polypeptide can reclaim from the reconstitution cell culture and purifying comes out, and the method for recovery and purifying has ammonium sulfate or ethanol sedimentation, acid extraction, negatively charged ion or cation-exchange chromatography, volume-exclusion chromatography, hydrophobic interaction chromatography, affinity chromatography, hydroxyapatite chromatography and phytohemagglutinin chromatography.Form ripe proteic complete conformation and also need proteinic refolding step.Usually high performance liquid chromatography (HPLC) or capillary electrophoresis can be applicable to last purification step.
Polynucleotide among the present invention and polypeptide can be used as research reagent and material, to find human treatment of diseases and diagnostic method.This polynucleotide and its encoded polypeptides also can be used for the research of external related science, DNA is synthetic and the preparation of dna vector, also are used to design the method for treatment and diagnosing human disease.
The fragment of total length OSGPLP gene can be as the hybridization probe in cDNA library, thereby isolates full-length gene and sequence similarity is highly arranged or other gene of similar biologic activity with it.Such probe generally has 20 bases at least.But these probes preferably have 30 bases at least and generally are no more than 50 bases, although they can have more base.This probe also can be used to identify corresponding to the cDNA clone of total length transcript or have complete genome, comprise the genomic clone of adjusting and promoter region, exon and intron.The screening a kind of method be, utilize known dna sequence dna to synthesize an oligonucleotide probe, remove to isolate the coding region of gene with it.Can be used for screening human cDNA library, genomic library, mRNA library with polynucleotide sequence complementary of the present invention through the oligonucleotide of mark, with determine in the library which member can with probe hybridization.
Can utilize partial nucleotide sequence and utilize the nucleotide sequence of means known in the art stretched-out coding OSGPLP, to detect its upstream sequence as promotor and controlling element.For example, can utilize universal primer to pass through restriction site PCR (RESTRICTION-SITE PCR) to give the unknown nucleotide sequence adjacent (Sarkar, G. (1993) PCR method is used (PCR MethodApplic.) 2:318-322) for change with the known seat.Utilize different primers by reverse transcription PCR amplification or extension sequence (Triglia, people such as T., (1988), nucleic acids research (Nucleic AcidsRes.) 16:8186) based on known region.Other available PCR method comprise catches PCR (capture PCR), carries out pcr amplification ((1991) PCR method is used 1:111-119 for Lagerstrom, people such as M) as the dna fragmentation with contiguous people and yeast artificial chromosome dna.In addition, those skilled in the art also can utilize nested primer (nested primer) and PromoterFinder by PCR TMThe library carry out the genomic dna walking (Clontech, Palo Alto, Calif.).
The invention still further relates to and utilize the OSGPLP gene product to detect and suddenly change relevant disease or of the polynucleotide sequence of OSGPLP the diagnostic method of the susceptibility of disease.These diseases are relevant with the mRNA and the encoded protein matter abnormal expression of OSGPLP gene of the present invention, malignant tumour for example, hemopathy, diseases such as immunological disease and all kinds of inflammation.
Can on the level of DNA, detect the individuality of OSGPLP transgenation with various technology.Diagnostic nucleic acid can obtain from patient's cell, for example blood, urine, saliva, examination of living tissue and necrotomy material.Genomic dna can be directly used in detection, also can be before check and analysis carries out enzyme process amplification people such as (, natural 324:163-166,1986) Saiki with PCR.RNA or cDNA also can be used for same purpose.For example, can be used to identify and analyze the sudden change of OSGPLP gene with the nucleic acid complementary PCR primer of coding OSGPLP gene.For example, from comparing the variation of generation with normal genotype, the size of amplified production can detect disappearance and/or insert sudden change.But, perhaps use radio-labeling OSGPLP antisense dna sequence to hybridize with the DNA and the sudden change of radiolabeled OSGPLP RNA hybridization check point of amplification.Digest or can distinguish the duplex of complete paired sequence and mispairing from the different or change of melting temperature(Tm) with RNA enzyme A.
By detecting the variation of dna fragmentation electrophoretic mobility in the gel that contains or do not contain denaturing agent, can carry out genetics test based on dna sequence dna difference.The disappearance of little sequence and insertion can be found out from high-resolution gel electrophoresis.For example, the dna fragmentation of different sizes can distinguish in denaturing polyacrylamide gel electrophoresis (PAGE).The dna sequence dna that contains point mutation can be distinguished and come in the polyacrylamide gel that does not contain denaturing agent after the sex change respectively with normal dna sequence dna because of different (the mobility speed differences) of conformation.
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.
Nuclease protection experiment can disclose the sequence variation of specific position, such as RNA enzyme and S1 enzyme protection method or chemical break method (people such as Cotton, institute of NAS reports 85:4397-4401,1985).
In a word, specific DNA sequence can detect with following method: the Southern engram technology of hybridization, RNA enzyme protection, chemistry fracture, direct dna sequencing or use restriction enzyme (for example, the polymorphism RFLP of limited fragment length) and genomic dna.
Except more traditional gel electrophoresis and dna sequencing method, the also available original position analyzing and testing of suddenling change is come out.
The present invention also relates to be used for detect the diagnostic method of the mRNA abnormal expression of various tissue OSGPLP genes.Methods such as the available reverse transcription PCR of the variation of mRNA level (RT-PCR), Northern trace, dot blot or RNA in situ hybridization detect.These methods are known for a person skilled in the art.
The invention still further relates to and be used for detecting the diagnostic method that various tissue OSGPLP gene protein levels change, compare the proteic minimizing detectable disease of OSGPLP or to exist (as malignant tumour, hemopathy, immunological disease and all kinds of inflammation etc.) of disease susceptibility with the normal control tissue sample.The method of measuring OSGPLP gene protein level in host's sample is well known to those skilled in the art, comprises radioimmunoassay, competitive binding assay method, western engram analysis, enzyme-linked immunosorbent assay and sandwich assay.Enzyme-linked immunosorbent assay (ELISA) (people such as Coligan, modern immunological method (Current Protocols in Immunology) volume 1, No.2, the 6th chapter, 1991) will be prepared the antigenic specific antibody at OSGPLP in advance, preferably monoclonal antibody.In addition, also to prepare the report antibody of anti-monoclonal antibody.Be connected with a detectable reagent on the report antibody, such as marks such as radio isotope, fluorescence or horseradish peroxidases.For example, from the host obtain sample and on a solid phase carrier incubation, polystyrene reactant plate for example, its albumen in can adsorption sample.Use a kind of nonspecific proteins such as bovine serum albumin (BSA) incubation then, any free protein binding site on the wrapper plate.Second step added monoclonal antibody incubation in plate, at this moment, monoclonal antibody with combine attached to the OSGPLP gene protein on the polystyrene reactant plate.All are not in conjunction with last monoclonal anti body and function damping fluid flush away.The report antibody that links to each other with horseradish peroxidase adds in the entering plate at this moment, the result report antibody just be combined in OSGPLP antigen on monoclonal antibody combine.Do not washed off in conjunction with last report antibody yet.The substrate that adds peroxidase then, the depth of formed color and typical curve are made comparisons in the regular hour, just can measure the content of OSGPLP gene protein in the patient samples of certain volume.
Competition assay also can be used for this detection.The antigenic specific antibody of OSGPLP is linked on the solid phase carrier, allow the OSGPLP of mark then and the sample that obtains from the host together by the quantity of solid phase carrier and certification mark thing, for example use the liquid phase scintillometer.The quantity of OSGPLP in the quantity of marker and the sample is relevant.Sandwich assay is similar to enzyme-linked immunosorbent assay, comprises dual-antigen sandwich method and double antibody sandwich method.In the double-antibody sandwich assay method, OSGPLP is by solid carrier, with the antibodies that is adsorbed on the solid phase carrier.Second kind of antibody is attached on the OSGPLP again.The third antibody be labeled and second kind of antibody had specificity, when it just is attached on second kind of antibody during by solid phase carrier, detect its quantity then.
Utilize the OSGPLP of mark in the receptors bind experiment, can detect the cell of expressing the OSGPLP acceptor.Can whether distinguish cell according to the existence of OSGPLP acceptor, thereby the basis of this cell of prediction to the susceptibility of OSGPLP activity is provided with its density.
OSGPLP of the present invention is as a kind of O-sialoglycoprotein enzyme sample albumen, polypeptide OSGPLP of the present invention, its biologically active derivatives or the agonist of direct administering therapeutic effective dose, antagonist, inhibitor for example can treat, alleviate and/or prevent, diseases such as malignant tumour, hemopathy, all kinds of inflammation, immunological disease.These diseases include but not limited to:
The tumour of various tissues: cancer of the stomach, liver cancer, lung cancer, the esophageal carcinoma, mammary cancer, leukemia, lymphoma, thyroid tumor, hysteromyoma, neuroblastoma, astrocytoma, ependymoma, glioma, colorectal carcinoma, malignant histocytosis, melanoma, teratoma, sarcoma, adrenal carcinoma, bladder cancer, osteocarcinoma, osteosarcoma, myelomatosis, bone marrow cancer, the cancer of the brain, uterus carcinoma, carcinoma of endometrium, carcinoma of gallbladder, colorectal carcinoma, thymus neoplasms nasal cavity and tumor of sinus of nose, nasopharyngeal carcinoma, laryngocarcinoma, tracheal neoplasm, mesothelioma of pleura, fibroma, fibrosarcoma, lipoma, liposarcoma, leiomyoma;
Various inflammation: atopic reaction, bronchial asthma, hypersensitivity pneumonitis, adult respiratory distress syndrome, the lung eosinophilia, sarcoidosis, rheumatoid arthritis, similar rheumatism sample sacroiliitis, osteoarthritis, cholecystitis, glomerulonephritis, immune-complex type glomerulonephritis, acute anterior uveitis, osteoporosis, dermatomyositis, urticaria, atopic dermatitis, hemochromatosis, polymyositis, Addison's disease, Graves' disease, chronic active hepatitis, intestines are answered acute syndromes, atrophic gastritis, systemic lupus erythematous, myasthenia gravis, multiple sclerosis, Green-barre syndrome, intracranial granuloma, the Wegener granulomatosis, the autoimmunity thyroiditis, the autoimmunity interstitial nephritis, ulcerative colitis, anaemia, pancreatitis, Crohn disease, myocarditis, atherosclerosis, multiple scleroderma, and the inflammation that causes of infection and wound etc.;
Disease of immune system: rheumatoid arthritis, chronic active hepatitis, acute anterior uveitis, gonococcal infection posterior joint inflammation, immune-complex type glomerulonephritis, myocarditis behind the gonococcal infection, systemic lupus erythematous, rheumatoid arthritis, scleroderma, polymyositis, myasthenia gravis, Green-barre syndrome, autoimmune hemolytic anemia, immunologic thrombocytopenic purpura, the autoimmunity interstitial nephritis, autoimmunity gastritis, autoimmune thyroid disease, the immunodeficient disease that phagocytic cell lacks, the defect of complement system disease, the Down syndromes, aplastic anemia, acquired immune deficiency syndrome (AIDS), bronchial asthma, Asprin asthma, rhinallergosis, supersensitivity broncho-pulmonary aspergillosis, hypersensitivity pneumonitis, diffuse interstitial pulmonary fibrosis, sarcoidosis, urticaria, atopic dermatitis;
The fragment of OSGPLP polypeptide and biologically active thereof, analogue and derivative can use in composition with pharmaceutical acceptable carrier, comprise polypeptide and the pharmaceutically acceptable carrier or the vehicle of dose therapeutically effective in such composition.Such carrier is including but not limited to salt solution, buffer saline, dextrose, water, glycerine, ethanol and combination thereof.Preparation should be fit to administering mode.
Pharmaceutical composition of the present invention also comprises the vaccine that utilizes polypeptide preparation of the present invention, it comprises that polypeptide of the present invention or its have the fragment of biologic activity or immunologic competence, wherein randomly also contains Freund's complete adjuvant, Freund's incomplete adjuvant and other pharmaceutically acceptable carrier.
The present invention also provides a kind of drug packages or test kit, comprises one or more containers that the composition of one or more pharmaceutical compositions of the present invention is housed.In addition, the fragment of these polypeptide and biologically active thereof, analogue and derivative also can be used in combination with other treatment compound.
These pharmaceutical compositions can be with the administration of a kind of mode easily, such as in epidermis, intravenously, intraperitoneal, intramuscular, the tumour, in subcutaneous, the nose or the intradermal approach.These pharmaceutical compositions use with the effective dose that becomes the concrete indication of prevention with treatment.
OSGPLP polynucleotide of the present invention can be used for gene therapy, through expression in vivo OSGPLP or utilize antisense technology and reach therapeutic purpose.
Gene therapy method for example comprises polynucleotide (DNA or the RNA) through engineering approaches of patient's cell being used coding OSGPLP polypeptide under the situation of exsomatizing, again the cell of through engineering approaches is supplied with patient to be treated.Such method is that everybody is familiar with in this area.For example, can carry out cell engineeringization with the retroviral particle of the RNA that comprises code book invention OSGPLP polypeptide.
Equally, with method known in the art in vivo the through engineering approaches cell with the expression in vivo polypeptide.As known in the art, the production cell that is used to produce the retroviral particle of the RNA that contains code book invention polypeptide can inject in the patient body, makes the cells in vivo through engineering approaches and expresses this polypeptide in vivo.From instruction of the present invention, these and other polypeptide administering mode is very clearly for those skilled in the art.For example except retrovirus, else be used for the expression vector of through engineering approaches cell in addition, adenovirus for example is it and through engineering approaches cell in vivo after a suitable transport agent combines.
The retrovirus that can derive above-mentioned retroviral plasmid vector includes but not limited to Moloney murine leukemia virus, spleen necrosis virus, Rous sarcoma virus, Harvey sarcoma virus, avian leukosis virus, gibbon ape leukemia virus, human immunodeficiency virus, adenovirus, myeloproliferative sarcoma virus and mammal tumor virus.
Can comprise one or more promotors in the above-mentioned carrier.Spendable suitable promotor includes but not limited to retroviral LTR, SV40 promotor, human cytomegalic inclusion disease virus (CMV) promotor (Miller: biotechnology (Biotechniques), volume 7, No.9, the 980-990 page or leaf, 1989) or other promotor (for example, the eukaryotic cell promotor includes, but are not limited to histone, pol III, beta-actin promotor).Other available viral promotors includes but not limited to adenovirus promoter, thymidine kinase (TK) promotor and B19 parvovirus promotor.From the instruction here, being chosen within those skilled in the art's ken of suitable promotor.
The polynucleotide sequence of code book invention polypeptide should be under the control of suitable promotor.Suitable promotor includes but not limited to that the promotor of adenovirus is such as adenovirus major late promoter; Or allogeneic promoter, such as cytomegalovirus (CMV) promotor; Respiratory syncytial virus (RSV) promotor; Inducible promoter is such as MMT promotor, metallothionein promoter; The heat-shocked promotor; Albumin promoter; ApoA I promotor; People's globin promotor; Viral thymidine kinase promoter is such as the herpes simplex thymidine kinase promoter; Retroviral LTR (the retroviral LTR that comprises modification described above); The beta-actin promotor; And human growth hormone promotor.It also can be self promotor of the gene of this polypeptide of control coding.
Form production clone with retroviral plasmid vector transduction package cell line.The packing cell that is used for transfection comprises, but be not restricted to, PE501, PA317, ψ-2, ψ-AM, PA12, T19-14X, VT-19-17-H2, ψ CRE, ψ CRIP, GP+E-86, GP+envAM12 and DNA clone, as Miller (human gene therapy (Human GeneTherapy) is described, volume 1, the 5-14 page or leaf, 1990), be incorporated herein by reference in full herein.The currently known methods of available this area carrier transduction package cell line.These methods include but not limited to, electroporation, use liposome and calcium phosphate precipitation.A kind of selectable method be the reverse transcription plasmid vector is wrapped up in the liposome or with the lipid coupling, inject the host then.
Production clone produces the infective retroviral particle of tool, comprises the nucleotide sequence of these polypeptide of encoding in this virion.Such retroviral vector particle can be used for external or the interior transfecting eukaryotic cells of body.Transfected eukaryotic cell will be expressed the nucleic acid encoding sequence.The eukaryotic cell that can be used for transfection includes but not limited to, embryonic stem cell, embryo cells, hemopoietic stem cell, liver cell, inoblast, sarcoplast, keratinocyte, endotheliocyte and bronchial epithelial cell.
On the other hand, utilize expression in vivo that antisense technology can change polypeptide of the present invention also with treatment relevant with expression of polypeptides disease.Can utilize the antisense molecule (DNA, RNA or peptide nucleic acid(PNA) (PNA)) of OSGPLP gene coding region, control or regulatory region.Recently, reported in the document and utilized the application (Gee of triple helical DNA in treatment, J.E. wait the people, (1994) in Huber, B.E. and B.I.Carr, molecule and immunological method (Molecular and ImmunologicApproaches), Futura Publishing Co., Mt.Kisco, N.Y., 163-177 page or leaf).Complementary sequence or antisense molecule also can combine to stop the translation of mRNA with ribosomal by preventing transcript.
" peptide nucleic acid(PNA) " is meant a kind of antisense molecule or anti-gene thing, and it comprises the oligonucleotide that is connected with the peptide backbone of the amino-acid residue that ends up with Methionin, and the length of oligonucleotide is at least 5 Nucleotide.Terminal Methionin is given the solvability to composition.Peptide nucleic acid(PNA) is preferentially in conjunction with complementary single stranded DNA or RNA, and the extension that termination is transcribed also can prolong its half life (Nielsen, people such as P.E., (1993) antitumor drug research (Anticancer DrugRes.) .8:53-63) in cell.
Polypeptide and fragment thereof, derivative or analogue or the cell of expressing them can be used as immunogen to produce its antibody.These antibody can be polyclone or monoclonal antibody.The present invention also comprised embedding and, strand and product humanized antibody and Fab fragment or Fab expression library.The whole bag of tricks known in the art can be used for such antibody and segmental generation.
The antibody at polypeptide of the present invention that is produced can obtain by directly polypeptide of the present invention being injected to animal or it being imported animal (preferably not being the people).Resulting antibody can combine with polypeptide is own.Also can obtain antibody in this way, even with a fragment sequence of code book invention polypeptide in conjunction with whole natural polypeptides.Then, antibody can be used to polypeptide is separated from the tissue of expressing it.
The preparation monoclonal antibody can be cultivated the technology that produces antibody with continuous cell line.For example, with hybridoma technology (Kohle ﹠amp; Milstein: natural 256:495-497,1975), Trioma technology, human B cell hybridoma technology (people such as Kozbor, immunology today (ImmunologyToday) 4:72,1983) and the EBV-hybridoma technology produce people's monoclonal antibody (people such as Cole, monoclonal antibody and cancer therapy (Monoclonal Antibodies and CancerTherapy), Alan R.Liss, Inc., 77-96,1985).
Single-chain antibody generating technique (United States Patent (USP) 4,946,778) is applicable to the single-chain antibody that produces immunogenic polypeptide product of the present invention.Transgenic animal also can be used to express the humanized antibody of immunogenic polypeptide product of the present invention.
The OSGPLP specific antibody can be used for the diagnosis and the treatment of relative disease.These antibodies and deactivation OSGPLP.
The invention still further relates to the method for agonist, antagonist and the inhibitor of a kind of OSGPLP of screening, comprise the molecule that can suppress or stimulate the OSGPLP function that uses polypeptide of the present invention or its fragment screening peptide library or drug candidates library to be used to seek therapeutic value.The screening of the agonist of polypeptide of the present invention, antagonist and inhibitor can utilize the known method of those of ordinary skills to carry out.The present invention also provides screening of medicaments to identify the method that improves (agonist) or check the active medicine of (antagonist) OSGPLP.Agonist improves OSGPLP and participates in comprising the many pathology of cell fission, fetal development, immunne response etc. and the activity of physiological process, and antagonist prevention and treatment and above-mentioned pathology or physiological process imbalance diseases associated such as muscle tissue tumor and tumor-like lesion.For example, the film preparation of mammalian cell or expression OSGPLP can be cultivated by the OSGPLP with mark in the presence of medicine.Measure the medicine raising then or check this interactional ability.The proteic antagonist of OSGPLP can and be eliminated its function with people OSGPLP protein binding, or suppresses the proteic generation of people OSGPLP, or combines with the avtive spot of polypeptide and to make polypeptide can not bring into play biological function.In SCREENED COMPOUND during as antagonist, people OSGPLP albumen that can this kind is new adds in the bioanalysis mensuration, determines by measuring new people OSGPLP proteinate influence of new this kind of people OSGPLP albumen of this kind and the interaction between its acceptor whether compound is antagonist.With the same quadrat method of above-mentioned SCREENED COMPOUND, can filter out the molecule of antagonist action.The OSGPLP that these obtain by the inventive method or its segmental agonist, antagonist and inhibitor can be mixed with pharmaceutical composition as mentioned above and be used for above-mentioned treatment of diseases.
The present invention will further describe in the following embodiments.But the present invention is not limited to these embodiment.All parts and amount, except as otherwise noted all by weight.
" digestion " of DNA refers to restriction enzyme DNA be carried out the catalytic cutting, and restriction enzyme only acts on the specific site of dna sequence dna.Here used various restriction enzymes can obtain from commerce, and their reaction conditions, cofactor and other requirement are according to the application known to the those skilled in the art.In order to analyze needs, in the buffered soln of about 20 μ l, add the enzyme of 1 μ g plasmid or dna fragmentation and about 2 units usually.For the DNA isolation fragment is used for plasmid construction, usually in a bigger volume with the DNA of enzymic digestion 5 to the 50 μ g of 20 to 250 units.Manufacturer can indicate the suitable damping fluid of special restriction enzyme and the amount of substrate.Usually the used incubation time approximately be 37 ℃ one hour, but can change to some extent according to the indication of producer.Directly on polyacrylamide gel, carry out electrophoresis after the restrictive diges-tion, isolate the fragment of wanting.
Separate available 8% polyacrylamide gel (people such as Goedde, nucleic acids research 8:4057,1980) according to the clip size that is cut into.
" connection " refers to form the process of phosphodiester bond between two double stranded nucleic acid fragments.Unless method for distinguishing is provided, connection can be carried out under known damping fluid and condition, and the dna fragmentation that is used to connect of the about equimolar amount of promptly every 0.5mg adds the T4 dna ligase of 10 units (" ligase enzyme ").
Except as otherwise noted, Graham ﹠amp is all used in conversion; Van der Eb: virusology (Virology) 52:456-457, the method described in 1973 is carried out.The clone of embodiment 1:OSGPLP
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 mRNAIsolation Kit (Qiegene company product).2 μ g poly (A) mRNA form 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 the sequence of 3 ' end with terminal circulating reaction sequencing kit (Perkin-Elmer company product) of dyestuff and ABI377 automatic sequencer (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 0234b07 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 0234b07 clone is 2058bp (shown in Seq ID NO:1), from 110bp to 1354bp the open reading frame (ORF) of a 1245bp, the new protein (shown in Seq ID NO:2) of encoding arranged.We are with this clone's called after pBS-0234b07, encoded protein matter called after OSGPLP.Embodiment 2:cDNA clone's homology retrieval
With sequence and the encoded protein sequence thereof of OSGPLP of the present invention, with Blast program (Basiclocal Alignment search tool) [Altschul, people such as SF, molecular biology magazine, 1990; 215:403-10], carry out the homology retrieval at databases such as Genbank, Swissport.The gene the highest with OSGPLP homology of the present invention is a kind of known possible O-sialoglycoprotein endopeptidase (gcp) [Rickettsia prowazekii], and its encoded protein number is AJ235270 in the access of Genbank.Protein homology the results are shown in Fig. 1, both height homologies, and its homogeny is 106/274 (38%); Similarity is 152/274 (55%).Embodiment 3: with the gene of RT-PCR method clones coding OSGPLP
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:
Primer 1:5 '-GTCGGGCTTTCTCCTGCAGCGATAA-3 ' (SEQID NO:3)
Primer 2: 5 '-TTGCCATCTTTTAAAAATTTTTTTATTTTTAA-3 ' (SEQ ID NO:4)
The forward sequence that primer 1 begins for the 5 ' 1bp that holds that is positioned at SEQ ID NO:1;
Primer 2 be SEQ ID NO:1 in 3 ' end reverse sequence.
The condition of amplified reaction: in the reaction volume of 50 μ l, contain 50mmol/LKCl, 10mmol/L Tris-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 ℃ 30 seconds; 55 ℃ 30 seconds; 72 ℃ 2 minutes.When RT-PCR, establish the blank negative contrast of positive contrast of beta-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 that the dna sequence dna of PCR product and the 1-2058bp shown in the SEQ ID NO:1 are identical.Embodiment 4:Northern blotting is analyzed the OSGPLP 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 OSGPLP coding region sequence (110bp to 1354bp) or its part of the pcr amplification shown in the SEQ ID NO:1.Will 32(about 2 * 106cpm/ml) spend the night in 42 ℃ of hybridization in following solution with the nitrocellulose filter that has shifted RNA the probe of P-mark, and 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 was washed 30 minutes in 55 ℃ in 1 * SSC-0.1%SDS.Then, analyze with quantitative with the phosphorus imager.Embodiment 5: vivoexpression, separation and the purifying of reorganization OSGPLP
According to the coding region sequence shown in the SEQ ID NO:1, design a pair of specificity amplification primer, sequence is as follows:
Primer 3:5 '-GGATCCATGCTAATCTTGACTAAGACTGCAGG-3 ' (Seq ID No:5)
Primer 4:5 '-CTCGAGTGAACAGCAGAAATCATATCTCCA-3 ' (SeqID No:6)
5 ' end of these two sections primers contains BamH I and Xho I restriction enzyme site respectively, be respectively the encoding sequence of target gene 5 ' end and 3 ' end thereafter, BamH I and Xho I 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-0234b07 plasmid that contains the total length goal gene is template, carries out the PCR reaction.The PCR reaction conditions is: contain pBS-0234b07 plasmid 10pg, 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 ℃ 20 seconds, 60 ℃ 30 seconds, 68 ℃ 2 minutes, totally 25 circulations.Respectively amplified production and plasmid pET-28 (+) are carried out double digestion with BamH I and Xho I, reclaim big fragment respectively, and connect with the T4 ligase enzyme.Connect the product conversion and transform big enterobacterial DH5 α, 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 Calcium Chloride Method.Select the correct positive colony of sequence (pET-0234b07) 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-0234b07) 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 OSGPLP of purifying.Through the SDS-PAGE electrophoresis, obtain single band (Fig. 2) at the 46kDa 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 hold 15 amino-acid residues identical with the N-shown in the SEQ ID NO:2 as a result.Embodiment 6 anti-OSGPLP production of antibodies
Synthesize the specific polypeptide of following OSGPLP with Peptide synthesizer (PE company product):
NH2-Met-Leu-Ile-Leu-Thr-Lys-Thr-Ala-Gly-Val-Phe-Phe-Lys-Pro-Ser-OH(SEQ?ID?NO:7)。Form compoundly with hemocyanin and bovine serum albumin coupling this polypeptide respectively, method waits the people, immunochemistry (Immunochemistry), 1969 referring to Avrameas; 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 OSGPLP specifically.The antisense oligonucleotide of embodiment 6:OSGPLP suppresses the propagation of HL-60 cell
Adopt 392 type dna synthesizers antisense oligonucleotide (AS-ODN) and the positive MODN (S-ODN) of synthetic OSGPLP automatically, and carry out chemically modified and become AS-PS-ODN and S-PS-ODN with two sulphur tetrem autumn nurses (TETD), its base sequence is:
AS-PS-ODN:5’-TCTTAGTCAAGATTAGCATACTTACTCT-3’
S-PS-ODN:5’-AGAGTAAGTATGCTAATCTTGACTAAGA-3’
With concentration is that 5 * 105HL-60 cell is divided into 3 groups and cultivates in the 37-5%CO2 incubator: (1) control group is simple HL-60 cell; (2) HL-60 cell+AS-PS-ODN (3) HL-60 cell+S-PS-ODN.The final concentration of AS-PS-ODN or AS-PS-ODN is 20 μ g/ml.Cell cultures detects the mortality ratio of cell with the blue dyeing of platform phenol after 24 hours.The result shows that AS-PS-ODN group cell mortality is 72.5%, and control group and S-PS-ODN group mortality ratio are 5%.Show that the antisense oligonucleotide of OSGPLP gene can suppress the propagation of HL-60 cell effectively.
Sequence table (1) general information: (ⅰ) applicant:
(A) name: Shengyuan Gene Development Co., Ltd., Shanghai
(B) street: No. 668 610 Room, East Road, Beijing
(C) city: Shanghai
(D) country: China
(E) postcode: 200001 (ⅱ) denomination of invention: a kind of O-sialoglycoprotein enzyme sample albumen and its polynucleotide sequence (ⅲ) the sequence number of encoding: the information of 7 (2) SEQ ID NO:1: (ⅰ) sequence signature:
(A) length: 2058bp
(B) type: nucleic acid
(C) chain: two strands
( D ) ： ( ⅱ ) ：cDNA ( ⅹⅰ ) ：SEQ ID NO:1: 1 GTCGGGCTTTCTCCTGCAGCGATAAGGGCAGTCGACAGTCTTTAGTAGGGAAAGGAGACA 61 AGTGCTAGCTACTGCCGCCCAAGTGGAAGGAATTATCTATAGAGTAAGTATGCTAATCTT121 GACTAAGACTGCAGGAGTTTTTTTTAAACCATCAAAAAGGAAAGTTTATGAATTTTTAAG181 AAGTTTTAATTTTCATCCTGGAACACTATTTCTTCATAAAATAGTATTGGGAATTGAAAC241 TAGTTGTGATGATACAGCAGCTGCTGTGGTGGATGAAACTGGAAATGTGTTGGGAGAAGC301 AATACATTCCCAAACTGAAGTTCATTTAAAAACAGGTGGGATTGTTCCTCCAGCAGCTCA361 ACAGCTTCACAGAGAAAATATTCAACGAATAGTACAAGAAGCTCTTTCTGCCAGTGGAGT421 CTCTCCAAGTGACCTCTCAGCAATTGCAACTACCATAAAACCAGGACTTGCTTTAAGCCT481 GGGAGTGGGCTTATCATTTAGCTTACAGCTGGTAGGACAGTTAAAAAAGCCATTCATTCC541 CATTCATCATATGGAGGCTCATGCACTTACTATTAGGTTGACCAATAAAGTAGAATTTCC601 TTTTTTAGTTCTTTTGATTTCTGGAGGTCACTGTCTGTTGGCATTAGTTCAAGGAGTTTC661 AGATTTTCTGCTTCTTGGAAAGTCTTTGGACATAGCACCAGGTGACATGCTTGACAAGGT721 GGCAAGAAGACTTTCTTTAATAAAACATCCAGAGTGCTCCACCATGAGTGGTGGGAAAGC 781 CATAGAACATTTGGCCAAACAAGGAAATAGATTTCATTTTGACATCAAACCTCCCTTGCA 841 TCATGCTAAAAATTGTGATTTTTCTTTTACTGGACTTCAACACGTTACTGATAAAATAAT 901 AATGAAAAAGGAAAAAGAGGAAGGTATTGAGAAGGGGCAAATCCTGTCTTCAGCAGCAGA 961 CATTGCTGCCACAGTACAGCACACAATGGCATGTCATCTTGTGAAAAGAACACATCGGGC1021 TATTCTGTTTTGTAAGCAGAGAGACTTGTTACCTCAAAATAATGCAGTACTGGTTGCATC1081 TGGTGGTGTCGCAAGTAACTTCTATATCCGCAGAGCTCTGGAAATTTTAACAAACGCAAC1141 ACAGTGCACTTTGTTGTGTCCTCCTCCCAGACTATGCACTGATAATGGCATTATGATTGC1201 ATGGAATGGTATTGAAAGACTACGTGCTGGCTTGGGCATTTTACATGACATAGAAGGCAT1261 CCGCTATGAACCAAAATGTCCTCTTGGAGTAGACATATCAAAAGAAGTTGGAGAAGCTTC1321 CATAAAAGTACCACAATTAAAAATGGAGATATGATTTCTGCTGTTCAAAAAAGTCCCTAA1381 AGGGTCTCACTCTCTGACCTCAGCTGGAGTACAGTAGCCAGATCACAACTCACTGCAACC1441 CTGACTTCCTGAACTCAAGAAATCCTCCTGCCTTAGCCTCTTGAATAGCCGGGACTACAG1501 GTGTGCATGTCCATGCCCAGCCAACTTTATTTCTATTTTTTGTAGAGACAGGCTCTTGCC1561 ATGTTGCCCGGGCTGGTCCTGAACTGCTGAATTCAAGTGATCCTCCCACCTTGGCCTCCA1621 GAAGTGCTGGGATTATGGGTGTGAGCCACCATGCCTAGCCAAAATGTTTCTTAAGGTATA1681 CATTTTGGGTCTTAGAAGACTTATACATTTGTAATATTTATTACTAAATATCTCAAAGTA1741 TTACAATAAATGTTACCATGTGAGCTACTTTGAATCAGGCTTCTTGCACACCAATTTAAA1801 AATGTTAACTCTTGATATATACACTAGTTATACCACTCATGTCAGTCAATAAATTTTAAG1861 GTTTAAGTGCAGGCCTTTGTTTACAGAAATCCTAATTTTTTGAAACCATAACTCTGACCT 1921 GACACTAAATTCCTGTAGACATGCTAAGGAAAATCTGCTTAGTATCGAGATCAAGAACTT1981 CCATTCAAAAAGATTATTCAGTTATGTTATTTGCATATTACCATTGTTAAAAATAAAAAA2041 ATTTTTAAAAGATGGCAA ( 3 ) SEQ ID NO:2： ( ⅰ ) ：
(A) length: 414 amino acid
(B) type: amino acid
( D ) ： ( ⅱ ) ： ( ⅹⅰ ) ：SEQ ID NO:2:1 Met Leu Ile Leu Thr Lys Thr Ala Gly Val Phe Phe Lys Pro Ser 16 Lys Arg Lys Val Tyr Glu Phe Leu Arg Ser Phe Asn Phe His Pro 31 Gly Thr Leu Phe Leu His Lys Ile Val Leu Gly Ile Glu Thr Ser 46 Cys Asp Asp Thr Ala Ala Ala Val Val Asp Glu Thr Gly Asn Val 61 Leu Gly Glu Ala Ile His Ser Gln Thr Glu Val His Leu Lys Thr 76 Gly Gly Ile Val Pro Pro Ala Ala Gln Gln Leu His Arg Glu Asn 91 Ile Gln Arg Ile Val Gln Glu Ala Leu Ser Ala Ser Gly Val Ser106 Pro Ser Asp Leu Ser Ala Ile Ala Thr Thr Ile Lys Pro Gly Leu121 Ala Leu Ser Leu Gly Val Gly Leu Ser Phe Ser Leu Gln Leu Val136 Gly Gln Leu Lys Lys Pro Phe Ile Pro Ile His His Met Glu Ala151 His Ala Leu Thr Ile Arg Leu Thr Asn Lys Val Glu Phe Pro Phe166 Leu Val Leu Leu Ile Ser Gly Gly His Cys Leu Leu Ala Leu Val181 Gln Gly Val Ser Asp Phe Leu Leu Leu Gly Lys Ser Leu Asp Ile196 Ala Pro Gly Asp Met Leu Asp Lys Val Ala Arg Arg Leu Ser Leu211 Ile Lys His Pro Glu Cys Ser Thr Met Ser Gly Gly Lys Ala Ile226 Glu His Leu Ala Lys Gln Gly Asn Arg Phe His Phe Asp Ile Lys241 Pro Pro Leu His His Ala Lys Asn Cys Asp Phe Ser Phe Thr Gly256 Leu Gln His Val Thr Asp Lys Ile Ile Met Lys Lys Glu Lys Glu271 Glu Gly Ile Glu Lys Gly Gln Ile Leu Ser Ser Ala Ala Asp Ile286 Ala Ala Thr Val Gln His Thr Met Ala Cys His Leu Val Lys Arg301 Thr His Arg Ala Ile Leu Phe Cys Lys Gln Arg Asp Leu Leu Pro316 Gln Asn Asn Ala Val Leu Val Ala Ser Gly Gly Val Ala Ser Asn331 Phe Tyr Ile Arg Arg Ala Leu Glu Ile Leu Thr Asn Ala Thr Gln346 Cys Thr Leu Leu Cys Pro Pro Pro Arg Leu Cys Thr Asp Asn Gly361 Ile Met Ile Ala Trp Asn Gly Ile Glu Arg Leu Arg Ala Gly Leu376 Gly Ile Leu His Asp Ile Glu Gly Ile Arg Tyr Glu Pro Lys Cys391 Pro Leu Gly Val Asp Ile Ser Lys Glu Val Gly Glu Ala Ser Ile406 Lys Val Pro Gln Leu Lys Met Glu Ile ( 4 ) SEQ ID NO:3 ( ⅰ )
(A) length: 25 bases
(B) type: nucleic acid
(C) chain: strand
(D) topological framework: linear (ⅱ) molecule type: oligonucleotide (ⅹ ⅰ) sequence description: information (ⅰ) sequence signature of SEQ ID NO:3:GTCGGGCTTT CTCCTGCAGC GATAA 25 (5) SEQ ID NO:4
(A) length: 32 bases
(B) type: nucleic acid
(C) chain: strand
(D) topological framework: linear (ⅱ) molecule type: oligonucleotide (ⅹ ⅰ) sequence description: information (ⅰ) sequence signature of SEQ ID NO:4:TTGCCATCTT TTAAAAATTT TTTTATTTTT AA 32 (6) SEQ ID NO:5
(A) length: 32 bases
(B) type: nucleic acid
(C) chain: strand
(D) topological framework: linear (ⅱ) molecule type: oligonucleotide (ⅹ ⅰ) sequence description: information (ⅰ) sequence signature of SEQ ID NO:5:GGATCCATGC TAATCTTGAC TAAGACTGCA GG 32 (7) SEQ ID NO:6
(A) length: 30 bases
(B) type: nucleic acid
(C) chain: strand
(D) topological framework: linear (ⅱ) molecule type: oligonucleotide
(xi) sequence description: the information of SEQ ID NO:6:CTCGAGTGAA CAGCAGAAAT CATATCTCCA 30 (8) SEQ ID NO:7: (ⅰ) sequence signature:
(A) length: 15 amino acid
(B) type: amino acid
(D) topological framework: linearity
(ⅱ) molecule type: polypeptide
(ⅹ ⅰ) sequence description: SEQ ID NO:7:Met-Leu-Ile-Leu-Thr-Lys-Thr-Ala-Gly-Val-Phe-Phe-Lys-Pro-Ser 15
(9) information of SEQ ID NO:8
(ⅰ) sequence signature (A) length: 28 bases (B) type: nucleic acid (C) chain: strand (D) topological framework: linearity
(ⅱ) molecule type: oligonucleotide
(ⅹ ⅰ) sequence description: SEQ ID NO:6:TCTTAGTCAA GATTAGCATA CTTACTCT 28
(10) information of SEQ ID NO:9
(ⅰ) sequence signature
(A) length: 28 bases
(B) type: nucleic acid (C) chain: strand (D) topological framework: linearity
(ⅱ) molecule type: oligonucleotide
(ⅹ ⅰ) sequence description: SEQ ID NO:6:AGAGTAAGTA TGCTAATCTT GACTAAGA 28

Claims (16)

1. isolating new people O-sialoglycoprotein enzyme sample albumen, it comprises polypeptide or its examples of conservative variations or its active fragments or the derivative with SEQ IDNo.2 aminoacid sequence.
2. polypeptide as claimed in claim 1, it is the polypeptide with SEQ ID No.2 aminoacid sequence.
3. isolating polynucleotide, it comprises a kind of nucleotide sequence or its variant that is selected from down group:
(a) polynucleotide of polypeptide as claimed in claim 1 or 2 of encoding;
(b) with polynucleotide (a) complementary polynucleotide;
(c) with (a) or polynucleotide sequence (b) have the polynucleotide of at least 70% homogeny.
4. polynucleotide as claimed in claim 3 is characterized in that, this polynucleotide encoding has the polypeptide of aminoacid sequence shown in the SEQ ID No.2.
5. polynucleotide as claimed in claim 3 is characterized in that, the sequence of these polynucleotide is selected from down a kind of of group:
(a) has the sequence of 110-1354 position among the SEQ ID No.1;
(b) has the sequence of 1-2058 position among the SEQ ID No.1.
6. recombinant vectors that contains the described polynucleotide of claim 3.
7. host cell with the described polynucleotide of claim 3 or the described recombinant vectors conversion of claim 6, transduction or transfection.
8. preparation method with polypeptide of the described polypeptide active of claim 1, this method comprises:
(a) being fit to express under the condition of the described polypeptide of claim 1, cultivate the described host cell of claim 7;
(b) from culture, isolate polypeptide with the described polypeptide active of claim 1.
9. energy and the described polypeptid specificity bonded of claim 1 antibody.
10. method of screening simulation, promotion, antagonism or suppressing the compound of the described polypeptide active of claim 1, it comprises polypeptide or its active fragments that utilizes claim 1.
11. the method for the disease that a vitro detection is relevant with the described polypeptide unconventionality expression of claim 1 or the susceptibility of disease comprises the sudden change of the described polypeptide of claim 1 in the detection of biological sample or its coded polynucleotide sequence.
12. according to the method for claim 11, wherein said polynucleotide are DNA or mRNA.
13. the method for the disease that a vitro detection is relevant with the described polypeptide unconventionality expression of claim 1 or the susceptibility of disease comprises the content or the biological activity of the described polypeptide of claim 1 in the detection of biological sample.
14. a pharmaceutical composition, it contains the combination of the described polypeptide of claim 1 or its stand-in, activator, antagonist or inhibitor or above each component, and it also comprises pharmaceutically acceptable carrier.
15. the polypeptide of claim 1 or the polynucleotide of claim 3 are used for the treatment of the purposes in the medicine of diseases such as various malignant tumours, hematologic disease, immunological disease and multiple inflammation in preparation.
16. the antisense polynucleotides of the antagonist of the described polypeptide of claim 1 or the described polypeptid coding sequence of claim 1 is used for the treatment of purposes in the medicine of various malignant tumours, hematologic disease, immunological disease and multiple inflammation in preparation.
CN 00106834 2000-04-19 2000-04-19 O-sialogycoproteinase-like protein and polynucleotide sequence for encoding it Pending CN1318550A (en)

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