抗SARS冠状病毒S1蛋白N端249至667的单克隆抗体的制.docx
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1、抗SARS冠状病毒SI蛋白N端249至667的单克隆抗体的制抗SAKS冠状病毒S1.蛋白N端249至667的单克隆抗体的制备与鉴定作者:温坤车小燕东广州510282;1;梅亚波1(1;丘立文1:廖志勇1;袁国勇2:1第一军医高校珠江医院中心试验室,广2香港高校微生物学系,香港)摘要:目的在获得了具有免疫原性的SARS冠状病毒S1.蛋白片段的基础上,制备和鉴定特异性抗该段S1.蛋白单克隆抗体(mAb).方法原核表达含S蛋白受体结合区的SARS冠状病毒S1.蛋白片段S1.c(N端249-667氨基酸残基),其免疫原性经SARS病人复原期血清鉴定后免疫BAI.B/C小鼠,按常规方法制备单克隆抗体,并
2、采纳E1.1.SA间接法、免疫荧光和免疫印迹进行筛选和鉴定。结果筛选出3株特异性针对SARS冠状病毒S1.蛋白N端249-667的mAb杂交瘤细胞株,IgC亚类鉴定1株为IgG1.,2株为1.gG2a,经免疫荧光鉴定与人冠状病毒株229E和0C43无交叉反应。结论获得3株抗SAKS冠状病毒S蛋白受体结合区特异性单克隆抗体,为建立新的SARS冠状病毒检测方法的和进一步探讨S蛋白的功能奠定了基础。关键词:SARS冠状病毒;单克隆抗体:刺突蛋白:受体结合区Preparationandcharacterizationofmonoc1.ona1.antibodiesagainstS1.domainatN
3、termina1.residues249to667ofSRS-associatedcoionavirusS1.proteinWENKun1.:MEIYa-bo1.;Q1.U1.i-wcn1.;1.IAOZhi-yong1.;YuenKwok-yung2;CHEXiao-yan1.!Centra1.1.aboratory,ZhujiangHospita1.,FirstMi1.itaryMedica1.University,Guangzhou510282,China;2DepartmentofMicrobio1.ogy,UniversityofHongKong,HongKong,China.Ab
4、stract:ObjectiveToprepareandcharacterizemonoc1.ona1.antibodies(mbs)againstS1.proteinofsevereacuterespirato-rysyndrome(SARS)-associatedcoronavirus(SARS-CoV).Methods6-His-taggedrecombinantfragmentatN-termina1.residues249to667ofSARS-CoVS1.proteininc1.udingSproteinreceptor-bindingdomainwasexpressedinE.c
5、o1.i.Theim-munogenicityofthisS1.domainwasidentifiedandusedtoimmunizeBA1.B/cmicefortheproductionofhybridomas.TheidentificationofthemAbsagainstthisS1.domainwasperformedusingindirectenzyme-1inkedimmunosorbentassay(E1.ISA),indirectimmunof1.uorescenceassay(IF)andWesternb1.otting,respective1.y.Resu1.tsThr
6、eehybridomasproducingmAbsspe-cifictotheS1.domainwasobtained,withare1.ativemo1.ecu1.armassof48500.Noneofthe3mAbswerereactivewithhumancoronaviruses229Eand0C43.TwooftheInAbSwereIgG2aisotype,andtheotherwasIgG1.Conc1.usionThisisthefirstre-portofnbsproducedagainstSproteinreceptor-bindingdomainofSARS-CoV.T
7、he3S1.-spccificmAbsmaybeusefu1.forfurtherstudyofthefunctionoftheSproteinandfordiagnosisofSARS-CoVinfection.Keywords:severeacuterespiratorysyndrome-associatedCOrOnaVirus;SARS-CoV;monoc1.ona1.antibody:spikeg1.ycoprotein;receptor-bindingdomainReceived:2004-01-03ThisworkissupportedastheKeyMedica1.Resear
8、chProjectforSARSPreventionsponsoredbytheMinistryofScienceandTechno1.ogyofChinaandbyGuangdongProvinceCorrespondingauthor:CHEXiao-yan,M.D.,ProfessorintheCentra1.1.aboratoryofZhujiangHospita1.,Te1.:86-20-61643592,Fax:86-20-61643592,E-mai1.:IinChe,chexiaoyanThetwoauthors,WENKunandMEIYa-bo,havemadeequa1.
9、contribu-tionstothiswork.nove1.coronavirushasbeenidentifiedasthema-jorcauseofseveracuterespiratorysyndrome(SARS)1.23,butthebio1.ogica1.functionsofthisSARS-associatedcoronavirus(SARS-CoV)remaincurrent1.ypoor1.ychar-acterized.Recentstudiesreportedthatangiotensin-con-vertingenzyme2(AEC2)cou1.dbeafuncti
10、ona1.receptorforSARS-CoVandthereceptor-bindingdomain(RBD)wasidentifiedintheN-termina1.residues17to274oftheS1.spikeproteinofthevirus4.SubsequentstudiesdemonstratedthattheRBDwas1.ocatedintheN-tcrmi-na1.residues303to5375orresidues318to5106.TheS1.proteinisa1.sofoundtobeatargetforinducingneu-tra1.izingan
11、tibodyresponsestoSARS-CoVinfection7.InspiteofthefactthatthefunctionofSproteinisnotfu1.1.yunderstood,S1.proteinseemstop1.ayakeyro1.eintheinitia1.virusinfection.Basedonthisunderstanding,themonoc1.ona1.antiodies(mbs)targetedatS1.domaincanbeapotentia1.1.yusefu1.too1.forthestudyofthefunc-tionofSproteinan
12、dforthediagnosisofSARS.Fur-thermore,theavai1.abi1.ityofb1.ockingantibodiesmaybemeaningfu1.inthetreatmentofSARS.Inthispaper,wereportthec1.oning,expressionandantigeniccharacterizationofthevariousfragmentsofS1.domainaswe1.1.asthepreparationandcharacter!zationofmAbsagainsttherecombinantproteinS1.cde-riv
13、edfromtheS1.proteincontainingtheN-termina1.residues249to667.MATERIA1.SANDMETHODSVirusandce1.11.inesHumancoronavirusstrains229E(No.VR740),0C43(No.VR759)andce1.1.1.inesVeroE6(No.CR1.-1586),MRC-5(No.CC1.-171),BS-C-I(No.CC1.-26)werea1.1.purchasedfromAmericanTypeCu1.tureCo1.1.ection(ATCC).P1.asmidsThep1.
14、asmidencodingS1.proteingene,pET_28b(+)/SI(402OO1.bp,HKU-39849),waskind1.yprovid-edbytheDepartmentofMicrobio1.ogy,UniversityofHongKong.TheexpressionvcctorPQE-30andM1.5strainofEscherichiaco1.iwerepurchasedfromQ1.A-GEN.ReagentsTherestrictionendonuc1.easesBamHIandHindIIIwerepurchasedfromNewEng1.andBio1.
15、abs,andKpn1.,PstI,ExTaq,dNTPandDN1.adderwerefromTaKaRa.NiresinwasobtainedfromQIAGEN.Freund,Sadju-vant,50%PEG1450so1.ution,HTandHTwerepur-chasedfromSigmaA1.drich.Goatanti-mouseIgM,IgG,IgG1.,IgG2a,IgG2bandIgG3peroxidaseconjugates,goatanti-humanIgGperoxidaseconjugates,goatan-ti-mouseIgGFITCconjugateand
16、aminoethy1.carbazo1.e(EC)sing1.eso1.utionweretheproductsofZYMED.RPMI1640cu1.turemediurnandfeta1.bovinoserumwerefromGibco-BR1.1.1.thechemica1.reagentsusedinthisstudywereofana1.ytica1.grade,andpreparedwithion-dep1.etedwater.Seraandanima1.sSerumsamp1.esofSARSpatientsforthisstudyweresero1.ogica1.1.yconf
17、irmedbyindirectimmunof1.uo-rescenceandenzyme-1inkedimmunosorbentassay(E1.ISA)8,andtheserafromhea1.thydonorswereusedascontro1.forthesameassay.Five6-week-o1.dfema1.eBA1.B/cmicewereprovidedbytheExperimenta1.Ani-ma1.CenterofFirstMi1.itaryMedica1.University.C1.oningS1.fragmentsintotheexpressionvectorandi
18、tsexpressionS1.geneencodingtheaminoacidresidues14to667ofthespikeproteinoftheSARS-CoVwasamp1.i-fiedbyPCRusingthefo1.1.owingprimers:5,-CGGGTCCAGTGACCTTGACCGGTGCACCAC-3,;5,-CGGGGTCCTTCGTTGAACTG-3,.TheS1.genewasdigestedwithBam1.1.IandKpnIand1.igatedintothecorrespondingrestrictionsitesinpQE-30p1.asmidtop
19、reparethepQE-30S1.Threegenefragmentsrespec-tivc1.yencodingtheaminoacidresidues14to248,249to445and219-667oftheS1.spikeproteinderivedfromS1.proteinwereobtainedbydigestionoftherecombi-nantp1.asmid(pQE-30S1.)withtherestrictionendonuc1.eases,a1.11igatedintothepQE-30p1.asmidaccordingtotheirrestrictionsite
20、sintheframeandupstreamoftheseriesof6histidineresiduesanddesignatedaspQE-30S1.a,pQE30S1.bandpQE30S1.crespective1.y.Thep1.asmidsweretransformedintocompetentM15ce1.1.sfo1.1.owingtheprotoco1.ofQIGENmanua1.Thestrainscontainingtherecombinantp1.asmidswerecu1.turedin1.uria-Bertanimediurn(1.Bmedium)withconti
21、nuousshakingat37Cti1.1.theODva1.ueofthemediumreached0.7,fo1.1.owedbyinductionwith1mmoI/1.isopropy1.-D-thioga1actopyranoside(IPTG)at30*Cfor4h.PurificationandWesternb1.otana1.ysisofS1.fragmentsThecu1.turedce1.1.swerecentrifugedandharvested.6-His-taggedrecombinantfragmentswerepurifiedus-ingNiresinunder
22、denaturingconditionaccordingtothemanufacturer,sinstructionsandana1.yzedbyWesternb1.otting.Thepurifiedproteinswereseparatedbysodi-umdodecy1.su1.fate(SDS)-po1.yacry1.amidege1.e1.ectro-phoresis(PAGE),ande1.ectrophoretica1.Iytransferredtopo1.yviny1.idenef1.uoride(PVDF)membraneswiththemethoddescribedprev
23、ious1.y9.Afterthetransfer,themembraneswereb1.ockedinPBS-Tcontaining7%de-fattedmi1.kfor2hatroomtemperatureandthenincu-batedrespective1.ywiththeserafromSARSpatientsandhea1.thydonorsatthedi1.utionof1:100intheb1.ockingbufferfor12hat4C.After6washes,themembraneswereincubatedwithperoxidaseconjugatetigoatan
24、ti-mouseIgGatthediIutionof1:500for1hatroomtemperature.ThemembraneswereincubatedwithAECsigna1.so1.utionfor10minatroomtemperatureaftersuf-ficientwashingandthereactionsterminatedwithdis-ti11.edwater.ImmunizationsThespecificimmunogenicityofthefragmentsdesignatedS1.cwascharacterizedbyWesternb1.ottingusi
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- SARS 冠状病毒 S1 蛋白 249 667 单克隆抗体
