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Rational Design of Peptide-Functionalized Surface Plasmon Resonance Sensor for Specific Detection of TNT Explosive

机译:特异性检测TNT炸药的肽功能表面等离振子共振传感器的合理设计

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摘要

In this study, a rationally-designed 2,4,6-trinitrotoluene (TNT) binding peptide derived from an amino acid sequence of the complementarity-determining region (CDR) of an anti-TNT monoclonal antibody was used for TNT detection based on a maleimide-functionalized surface plasmon resonance (SPR) sensor. By antigen-docking simulation and screening, the TNT binding candidate peptides were obtained as TNTHCDR1 derived from the heavy chain of CDR1, TNTHCDR2 derived from CDR2, and TNTHCDR3 from CDR3 of an anti-TNT antibody. The binding events between candidate peptides and TNT were evaluated using the SPR sensor by direct determination based on the 3-aminopropyltriethoxysilane (APTES) surface. The TNT binding peptide was directly immobilized on the maleimide-functionalized sensor chip surface from N-γ-maleimidobutyryl-oxysuccinimide ester (GMBS). The results demonstrated that peptide TNTHCDR3 was identified and selected as a TNT binding peptide among the other two candidate peptides. Five kinds of TNT analogues were also investigated to testify the selectivity of TNT binding peptide TNTHCDR3. Furthermore, the results indicated that the APTES-GMBS-based SPR sensor chip procedure featured a great potential application for the direct detection of TNT.
机译:在这项研究中,将基于抗TNT单克隆抗体互补决定区(CDR)氨基酸序列的合理设计的2,4,6-三硝基甲苯(TNT)结合肽用于基于TNT的TNT检测。马来酰亚胺功能化的表面等离子体共振(SPR)传感器。通过抗原对接模拟和筛选,获得了TNT结合候选肽,其为来自CDR1的重链的TNTHCDR1,源自CDR2的TNTHCDR2和来自抗TNT抗体的CDR3的TNTHCDR3。使用SPR传感器通过基于3-氨基丙基三乙氧基硅烷(APTES)表面的直接测定来评估候选肽与TNT之间的结合事件。 TNT结合肽直接从N-γ-马来酰亚胺基丁酰-氧琥珀酰亚胺酯(GMBS)固定在马来酰亚胺官能化的传感器芯片表面上。结果表明,在其他两个候选肽中,已鉴定出肽TNTHCDR3并将其选作TNT结合肽。还研究了五种TNT类似物以证明TNT结合肽TNTHCDR3的选择性。此外,结果表明,基于APTES-GMBS的SPR传感器芯片程序具有直接检测TNT的巨大潜力。

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