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特异结合人禽流感病毒H5N1的scFv分子生物学活性性能鉴定
The detection of binding activity of phage display antibody to H5N1
【作者】 武婕; 柯昌文; 李晖; 陈秋霞; 周杰; 张欣; 邹丽容;
【Author】 Wu Jie,Ke Changwen,Li Hui,et al.Guangdong Provincial Center for Disease Control and Prevention,
【机构】 广东省疾病预防控制中心病原微生物检验所;
【摘要】 目的从人源化噬菌体抗体库(Human Single Fold scFv Libraries I+J)中筛选到能高亲和性、特异结合人禽流感病毒H5N1的单链抗体,为建立H5N1快速筛查试剂和人源化治疗单抗奠定基础。方法以H5N1病毒的血凝素(hemagglutitin,HA)蛋白和核蛋白(nucleoprotein,NP)为目的蛋白,对上述单抗噬菌体文库以亲和性为原理进行筛选,经过三轮筛选富集后,随机挑选了96个噬菌体克隆扩增培养,ELISA法挑选能特异性、高亲和性结合目的蛋白的噬菌体克隆,并换用HB2151宿主菌对阳性单链抗体克隆进行可溶性表达,ELISA法鉴定可溶性单链抗体的结合活性,PCR扩增阳性克隆的轻、重链基因片段,并对阳性单链抗体分子测序和序列分析。结果经过三轮筛选,分别从96个噬菌体克隆中挑选到了两株能特异结合NP蛋白、三株能特异结合HA蛋白的单链抗体,PCR扩增都得到了长为300bp、302bp和935bp的轻链、重链和轻链-连接片段-重链的基因片段,测序结果分析发现上述五条单链抗体片段在轻链的47、49、50、51、53、54、56、96、97、98和99位的氨基酸组成不同,而特异结合NP蛋白的单链在重链区域氨基酸组成完全相同,而特异结合HA蛋白的单链在重链的44、47、85、86、87、88和89位氨基酸组成不同。结论从噬菌体抗体库中筛选到的特异结合HA和NP蛋白的单链抗体片段,可为进一步研发H5N1快速筛选试剂和人源性治疗抗体奠定基础,也可为鉴定HA和NP蛋白中的抗原决定簇提供结构信息。
【Abstract】 Objective To select single-chain variable fragment(scFv) antibody specific for human H5N1 virus from Human Single Fold scFv Libraries.Methods Human Single Fold scFv Libraries were panned against immobilized HA and NP of H5N1 in a microtiter plate,after three rounds of panning,96clones were determined specific binding to the target protein.The specificity of each ScFv clone was determined by ELISA.Positive clones were expressed in HB2151 for production of soluble antibody fragment which were detected by ELISA。The light and heavy chain genes of positive ScFv were amplified and sequenced.Results After three round of panning,scFv for NP and HA had specific combination character.The gene fragments of 300bp,302bp and 935bp of light chain,heavy chain and joint gene were amplified with.The insertion gene fragment were correct of positive scFV.The DNA sequence data showed that there were 11 differences of the amino acids at 47、49、50、51、53、54、56、 96、97、98 and 99 sites in light chain among 5 positive scFV.There were no difference in heavy chain of anti-NP ScFv,while there were 7differences of amino acids at 44、47、 85、86、87、88 and 89 sites of anti-HA ScFv.Conclusion The specific ScFvs to HA and NP could be candidate for reagent to detect and prevent the infection of H5N1 virus.And the sequence of scFV will help to provide the clues of antigenic determinant epitopes of HA and NP protein.
- 【会议录名称】 新发和再发传染病防治热点研讨会论文集
- 【会议名称】新发和再发传染病防治热点研讨会
- 【会议时间】2011-12-01
- 【会议地点】中国广东珠海
- 【分类号】R392.1
- 【主办单位】中华医学会医学病毒学分会、广东省预防医学会医学病毒学专业委员会、广东省免疫学会