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李新鸣, 孙冶, 海晓欧, 黄天龙, 杜歌, 王凤杰, 齐金萍, 肖纯凌. 鼠源抗烟曲霉单链抗体库制备及鉴定[J]. 中国公共卫生, 2016, 32(11): 1590-1593. DOI: 10.11847/zgggws2016-32-11-38
引用本文: 李新鸣, 孙冶, 海晓欧, 黄天龙, 杜歌, 王凤杰, 齐金萍, 肖纯凌. 鼠源抗烟曲霉单链抗体库制备及鉴定[J]. 中国公共卫生, 2016, 32(11): 1590-1593. DOI: 10.11847/zgggws2016-32-11-38
LI Xin-ming, SUN Ye, HAI Xiao-ou.et al, . Preparation and characterization of a murine single chain antibody library against Aspergillus fumigatus[J]. Chinese Journal of Public Health, 2016, 32(11): 1590-1593. DOI: 10.11847/zgggws2016-32-11-38
Citation: LI Xin-ming, SUN Ye, HAI Xiao-ou.et al, . Preparation and characterization of a murine single chain antibody library against Aspergillus fumigatus[J]. Chinese Journal of Public Health, 2016, 32(11): 1590-1593. DOI: 10.11847/zgggws2016-32-11-38

鼠源抗烟曲霉单链抗体库制备及鉴定

Preparation and characterization of a murine single chain antibody library against Aspergillus fumigatus

  • 摘要: 目的 构建鼠源抗曲霉菌单链抗体(scFv)噬菌体展示文库并进行初步鉴定,为制备用于侵袭性曲霉感染实验室诊断的特异性抗体提供新的方法。方法 利用噬菌体展示技术构建鼠源抗烟曲霉半乳甘露聚糖(GM)ScFv库,经过4轮“吸附-洗脱-扩增”淘选富集,随机挑选克隆进行可变区基因测序确定文库多样性,并用phage-ELISA筛选烟曲霉特异性结合的克隆。结果 构建的scFv噬菌体表达文库,库容量约为1.8×107;经4轮富集筛选,洗脱的表达scFv噬菌体滴度渐增;随机挑选出4轮筛选后的20个克隆,其可变区基因序列不同;随机挑选出4轮筛选后的90个克隆,其中6个克隆与烟曲霉GM特异性结合,而与对照的白假丝酵母菌无结合。结论 构建并初步鉴定了抗曲霉菌单链抗体库,库容量大,VH和VL区具备多样性;筛选的scFv与曲霉菌GM特异性结合,提供了快速制备、筛选GM高特异性抗体分子的新方法。

     

    Abstract: Objective To construct a murine single chain antibody(scFv)library against galactomannan(GM)of Aspergillus fumigatus with phage display technique and to enrich and select specific anti-GM single chain antibodies and to identify the antibody library.Methods The total RNA was extracted from the spleen of mice immunized with Aspergillus fumigatus GM.The antibody VH and VL genes were amplified with real-time reverse transcription PCR(RT-PCR),and the VH and VL fragments were linked by overlapping PCR.The linked scFv fragments were transformed into pCANTAB5E phage display system,and the phage display library of scFv was constructed with the assistance of the helper phage.Immunotubes coated with gradient GM antigens were used for the screening of the murine natural source scFv phage antibody library.After four rounds of "absorption-elution-amplification" panning,positive clones obtained were sequenced and binding activity of scFv clones were detected with phage-enzyme-linked immunosorbent assay(ELISA).Results The phage display library of scFv against Aspergillus GM was constructed,which was about 1.8×107 clones in capacity.Using Aspergillus GM coated immune test tubes,the phage titers were increased after 4 rounds of panning.Twenty clones with different gene sequence of variable region were randomly selected after 4 rounds of panning.The diversity of VH and VL was confirmed in the single chain antibody library.Ninety clones were tested for binding specificity to Aspergillus GM.Phage-ELISA results showed that 6 clones have specific binding reactions only with Aspergillus GM,while no binding reaction with Candida albicans.Conclusion A murine scFv phage display library was constructed and identified preliminarily.The antibody library constructed presents a high connection rate of variable fragments,good diversity and large storage capacity.ScFv clones have specific binding activity with Aspergillus GM.The study provides a base for further screening of high specific antibody against galactomannan of Aspergillus fumigatus.

     

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