固定化金属亲和层析法从噬菌体展示文库中分离人戊型肝炎病毒抗体。

Ying-Wei Chen, Wen-Xin Luo, Ming-Qiao Wang, Jin Wang, Li-Feng Li, Quan Yuan, Jun Zhang, Ning-Shao Xia
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摘要

目的:采用基于固定化金属亲和层析(IMAC)的噬菌体抗体文库筛选新方法,从噬菌体展示文库中分离人戊型肝炎病毒抗体。方法:将噬菌体抗体文库与hex-His标记的表达HEV特异性抗原NE2混合,充分结合后加入hex-His亲和树脂。通过大量洗涤去除非特异性噬菌体抗体,然后将特异性结合的噬菌体抗体洗脱以感染TG1或重复结合过程进行后续纯化。通过抗原竞争ELISA、人血清阻断ELISA、scFv表达和序列分析检测所选人抗体的特异性。结果:经过筛选,成功富集了His-NE2特异性重组噬菌体。两个噬菌体克隆126和138在NE2抗原竞争ELISA中表现出50%的抑制作用,在阻断ELISA中被HEV阳性血清有明显的阻断作用。可溶性scFv 126,138特异地与NE2结合。结论:应用固定化金属亲和层析技术从噬菌体展示文库中分离到两种抗戊型肝炎病毒(HEV)的特异性噬菌体抗体。固定化金属亲和层析法用于噬菌体抗体的选择是对溶液选择的有益补充。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Isolation of human antibodies against hepatitis E virus from phage display library by immobilized metal affinity chromatography.

Objective: To isolate human antibodies against hepatitis E virus from phage display library by a new method of panning phage antibody library based on immobilized metal affinity chromatography (IMAC).

Methods: Phage antibody library was allowed to mix with hex-His tagged expressed HEV specific antigen, NE2, in solution for adequate binding before affinity resin for hex-His was added. The non-specific phage antibodies were removed by extensive washing and the specific bound phage antibodies could then be eluted to infect TG1 or repeat the binding process for subsequent rounds of purification. The specificity of the selected human antibodies were tested by antigen competitive ELISA, human sera blocking ELISA, scFv expression, and sequence analysis.

Results: His-NE2 specific recombinant phages were successfully enriched after panning procedure. Two individual phage clones, 126 and 138, showed 50% inhibition in NE2 antigen competition ELISA and obvious blocking effect by HEV positive serum in blocking ELISA. Soluble scFv of 126, 138 bound to NE2 specifically.

Conclusion: Two specific human phage antibodies against hepatitis E virus (HEV) from phage display library were isolated by immobilized metal affinity chromatography. The immobilized metal affinity chromatography applied to phage antibody selection was a helpful supplement to the selection in solution.

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