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基于阵列的理性设计短肽探针衍生自抗 TNT 单克隆抗体。

Array-Based Rational Design of Short Peptide Probe-Derived from an Anti-TNT Monoclonal Antibody.

机构信息

Department of Chemical Science and Engineering, School of Materials and Chemical Technology, Tokyo Institute of Technology , 2-12-1, O-okayama, Meguro-ku, Tokyo 152-8552, Japan.

JST, ImPACT, Sanban-cho 5, Chiyoda-ku, Tokyo 102-0075, Japan.

出版信息

ACS Comb Sci. 2017 Oct 9;19(10):625-632. doi: 10.1021/acscombsci.7b00035. Epub 2017 Sep 8.

Abstract

Complementarity-determining regions (CDRs) are sites on the variable chains of antibodies responsible for binding to specific antigens. In this study, a short peptide probe for recognition of 2,4,6-trinitrotoluene (TNT), was identified by testing sequences derived from the CDRs of an anti-TNT monoclonal antibody. The major TNT-binding site in this antibody was identified in the heavy chain CDR3 by antigen docking simulation and confirmed by an immunoassay using a spot-synthesis based peptide array comprising amino acid sequences of six CDRs in the variable region. A peptide derived from heavy chain CDR3 (RGYSSFIYWF) bound to TNT with a dissociation constant of 1.3 μM measured by surface plasmon resonance. Substitution of selected amino acids with basic residues increased TNT binding while substitution with acidic amino acids decreased affinity, an isoleucine to arginine change showed the greatest improvement of 1.8-fold. The ability to create simple peptide binders of volatile organic compounds from sequence information provided by the immune system in the creation of an immune response will be beneficial for sensor developments in the future.

摘要

互补决定区(CDRs)是抗体可变链上负责与特定抗原结合的位点。在这项研究中,通过测试源自抗 2,4,6-三硝基甲苯(TNT)单克隆抗体 CDRs 的序列,鉴定出一种用于识别 TNT 的短肽探针。通过抗原对接模拟,确定该抗体中的主要 TNT 结合位点位于重链 CDR3 中,并通过使用基于斑点合成的肽阵列的免疫测定法进行了验证,该阵列包含可变区中六个 CDRs 的氨基酸序列。通过表面等离子体共振测量,从重链 CDR3 衍生的肽(RGYSSFIYWF)与 TNT 的解离常数为 1.3 μM。用碱性残基取代选定的氨基酸可增加 TNT 的结合,而用酸性氨基酸取代则降低亲和力,异亮氨酸到精氨酸的变化显示出最大的 1.8 倍的改善。从免疫系统在免疫反应中产生的序列信息中创建针对挥发性有机化合物的简单肽结合物的能力将有益于未来传感器的发展。

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