中华微生物学和免疫学杂志
中華微生物學和免疫學雜誌
중화미생물학화면역학잡지
CHINESE JOURNAL OF MICROBIOLOGY AND IMMUNOLOGY
2011年
10期
938-941
,共4页
丁士标%李召东%严杰%林旭瑷
丁士標%李召東%嚴傑%林旭璦
정사표%리소동%엄걸%림욱애
问号钩端螺旋体%表位%属特异性抗原%免疫原性
問號鉤耑螺鏇體%錶位%屬特異性抗原%免疫原性
문호구단라선체%표위%속특이성항원%면역원성
Leptospira interrogans%Epitope%Genus-specific antigen%Immunogenicity
目的 构建问号钩端螺旋体(简称钩体)LipL32、OmpL1和LipL21蛋白的优势T-和B-细胞联合表位融合基因及其原核表达系统,并对表达产物的免疫原性进行鉴定.方法 人工合成多表位联合基因并构建其原核表达系统.采用SDS-PAGE检测重组蛋白;采用MAT检测重组蛋白兔抗血清与我国钩体标准参考株的凝集效价;Western blot和ELISA检测重组蛋白的免疫原性.结果 获得了多表位融合基因并构建了原核表达系统.表达产物的相对分子质量约为23×103,且主要以可溶性形式存在;重组蛋白兔抗血清免疫双扩散效价为1∶8,该抗血清能与我国15群的钩体标准参考株发生凝集反应,ELISA证明该重组蛋白能检测不同群型钩体感染患者血清中的抗钩体抗体.结论 成功构建了包含钩体LipL32、OmpL1和LipL21蛋白的优势T和B细胞联合表位基因及其原核表达系统,表达产物具有良好的抗原性和交叉免疫反应性,可作为研制通用型问号钩体基因工程疫苗及血清学检测的抗原.
目的 構建問號鉤耑螺鏇體(簡稱鉤體)LipL32、OmpL1和LipL21蛋白的優勢T-和B-細胞聯閤錶位融閤基因及其原覈錶達繫統,併對錶達產物的免疫原性進行鑒定.方法 人工閤成多錶位聯閤基因併構建其原覈錶達繫統.採用SDS-PAGE檢測重組蛋白;採用MAT檢測重組蛋白兔抗血清與我國鉤體標準參攷株的凝集效價;Western blot和ELISA檢測重組蛋白的免疫原性.結果 穫得瞭多錶位融閤基因併構建瞭原覈錶達繫統.錶達產物的相對分子質量約為23×103,且主要以可溶性形式存在;重組蛋白兔抗血清免疫雙擴散效價為1∶8,該抗血清能與我國15群的鉤體標準參攷株髮生凝集反應,ELISA證明該重組蛋白能檢測不同群型鉤體感染患者血清中的抗鉤體抗體.結論 成功構建瞭包含鉤體LipL32、OmpL1和LipL21蛋白的優勢T和B細胞聯閤錶位基因及其原覈錶達繫統,錶達產物具有良好的抗原性和交扠免疫反應性,可作為研製通用型問號鉤體基因工程疫苗及血清學檢測的抗原.
목적 구건문호구단라선체(간칭구체)LipL32、OmpL1화LipL21단백적우세T-화B-세포연합표위융합기인급기원핵표체계통,병대표체산물적면역원성진행감정.방법 인공합성다표위연합기인병구건기원핵표체계통.채용SDS-PAGE검측중조단백;채용MAT검측중조단백토항혈청여아국구체표준삼고주적응집효개;Western blot화ELISA검측중조단백적면역원성.결과 획득료다표위융합기인병구건료원핵표체계통.표체산물적상대분자질량약위23×103,차주요이가용성형식존재;중조단백토항혈청면역쌍확산효개위1∶8,해항혈청능여아국15군적구체표준삼고주발생응집반응,ELISA증명해중조단백능검측불동군형구체감염환자혈청중적항구체항체.결론 성공구건료포함구체LipL32、OmpL1화LipL21단백적우세T화B세포연합표위기인급기원핵표체계통,표체산물구유량호적항원성화교차면역반응성,가작위연제통용형문호구체기인공정역묘급혈청학검측적항원.
Objective To construct the T-cells and B-cells combined epitope peptide gene based on the LipL32,OmpL1 and LipL21 protein from Leptospira interrogans and E.coli expression system,and better understanding of the immunological activity of the recombinant protein. Methods The immunodomaint T- and B-cells combined epitopes of LipL32,OmpL1 and LipL21 were identified and used to synthetic a new gene and then construct its prokaryotic expression system.The expression of recombinant protein was determined by SDS-PAGE; MAT was used to determine the titer of the antiserum to L. interrogans standard strains of China ; Western blot and ELISA were used to identify the immunity activity of the recombinant protein.Results The synthetic gene was effectively expressed in E.coli BL21 ( DE3 ) strain and mainly presented in dissoluble protein.Western blot result showed that the expression protein react well with the antibodies from immunized rabbit by Leptospira or recombinant protein.ELISA and MAT results showed that the multiepitope protein could cross-react with different serogroup or serovar of Leptospira.Conclusion In this study,we successfully constructed the recombinant T- and B-cells combine epitope gene of leptospires and expressed it in E.coli.The recombinant protein had a good immune activity,and could cross-reacted with antibodies from different serogroups Leptospira infected patients.