检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:高云山 桑雨浓 梁夏夏 刘建欣 王文彬 GAO Yunshan;SANG Yunong;LIANG Xiaxia;LIU Jianxin;WANG Wenbin(Jiangsu Key Laboratory of Marine Biotechnology,Jiangsu Ocean University,Lianyungang 222005,China;Jiangsu Key Laboratory of Marine Bio-resources and Environment,Jiangsu Ocean University,Lianyungang 222005,China;Co-innovation Center of Jiangsu Marine Bio-industry Technology,Lianyungang 222005,China)
机构地区:[1]江苏海洋大学江苏省海洋生物技术重点实验室,江苏连云港222005 [2]江苏海洋大学江苏省海洋生物资源与环境重点实验室,江苏连云港222005 [3]江苏省海洋生物产业技术协同创新中心,江苏连云港222005
出 处:《江苏海洋大学学报(自然科学版)》2020年第2期15-21,共7页Journal of Jiangsu Ocean University:Natural Science Edition
基 金:江苏海洋大学江苏省海洋生物技术重点实验室开放课题(HS2019003);江苏省研究生科研与实践创新计划项目(SJCX19_0952)。
摘 要:外膜蛋白OmpK在弧菌属中保守性大于79%,是有良好应用前景的诊断和疫苗抗原,但弧菌属保守并且暴露在膜外的OmpK肽段有限,多肽免疫原免疫效果相比完整蛋白可能更具优势。采用Protein蛋白序列分析软件分析弧菌外膜蛋白OmpK,筛选出2条在弧菌属内广泛保守,同时亲水性和表面暴露性较好的多肽P1和P2。将合成的多肽与BSA蛋白偶联制备成多肽免疫原,免疫BALB/c小鼠,制备抗血清。间接ELISA结果显示,2条多肽免疫原抗血清对OmpK蛋白的效价均达到1∶81000,对弧菌菌体的效价P1-BSA免疫血清高于P2-BSA免疫血清。通过Western blot分析发现,多肽的抗血清均能与重组OmpK蛋白(27 kDa)以及测试的7株副溶血弧菌和1株创伤弧菌全菌蛋白发生免疫反应,P1多肽抗血清与2株气单胞菌,P2多肽抗血清与3株肠杆菌,存在不同程度的交叉反应。结果表明,OmpK的P1和P2多肽是弧菌共有的抗原表位,免疫血清对菌体识别较弱的原因有待进一步研究。The homology of outer membrane protein OmpK in Vibrio is more than 79%,and is a promising diagnostic and vaccine antigen.However,the conserved and surface-exposed epitopes on OmpK are usually very limited and may have advantages over intact protein as immunogen.In this study,the protein sequence of OmpK of Vibrio was analyzed by bioinformatics software(Protein),two conserved and hydrophilic peptides P1 and P2 were selected and studied for their immunogenicity.Peptide immunogens were prepared by coupling the synthesized polypeptide with carrier protein BSA,and BALB/c mice were immunized to prepare antiserum.Indirect ELISA results showed that the antisera titer of the two peptide immunogens against OmpK protein both reached 1∶81 000.The titer of P1-BSA against Vibrio spp.was higher than the titer of P2-BSA against Vibrio spp.Western blotting showed that the antiserum of the two peptides both strongly reacted with the recombinant OmpK protein(27 kDa)and whole bacterial protein of seven strains of V.parahaemolyticus and one strain of V.vulnificus.Furthermore,antiserum against P1 crossly reacted with two strains of Aeromonas and antiserum against P2 cross-reacted with three strains of Enterobacteriaceae.The results indicate that P1 and P2 polypeptides are the conserved epitopes of Vibrio,and further study is urged to understand the low binding of antiserum against the Vibrio cells.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.31