Highly Selective Rational Design of Peptide-Based Surface Plasmon Resonance Sensor for Direct Determination of 2,4,6-trinitrotoluene (TNT) Explosive

被引:43
作者
Wang, Jin [1 ,2 ]
Muto, Masaki [2 ,3 ]
Yatabe, Rui [1 ,2 ]
Tahara, Yusuke [1 ]
Onodera, Takeshi [1 ,4 ]
Tanaka, Masayoshi [2 ,3 ]
Okochi, Mina [2 ,3 ]
Toko, Kiyoshi [1 ,2 ,4 ]
机构
[1] Kyushu Univ, Res & Dev Ctr Taste & Odor Sensing, Nishi Ku, 744 Motooka, Fukuoka 8190395, Japan
[2] ImPACT, JST, Chiyoda Ku, Sanban Cho 5, Tokyo 1020075, Japan
[3] Tokyo Inst Technol, Dept Chem Sci & Engn, Meguro Ku, 2-12-1 O Okayama, Tokyo, Japan
[4] Kyushu Univ, Dept Informat Sci & Elect Engn, Nishi Ku, 744 Motooka, Fukuoka 8190395, Japan
关键词
TNT binding peptide; Amino acid sequence; Complementarity determining region; Surface plasmon resonance sensor; SENSITIVE DETERMINATION; SPR IMMUNOSENSOR; NANOSENSOR; BINDING; DERIVATIVES; ASSAY;
D O I
10.1016/j.snb.2018.02.075
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In this study, 2,4,6-trinitrotoluene (TNT) binding peptide was synthesized and screened for TNT specific detection using surface plasmon resonance (SPR) sensor. The TNT binding peptide was rational design and synthesized through amino acid sequence from complementarity determining region (CDR) in the anti-TNT monoclonal antibody, which was produced from hybridoma cell using TNP-KLH conjugate as antigen. Three TNT binding peptide sequences were obtained from the heavy chain of CDR1 named TNTHCDRI, TNTHCDR2 from CDR2 and TNTHCDR3 from CDR3 of anti-TNT antibody. Screening process of three candidate peptides were carried out by using the SPR sensor with direct determination, which the peptide was directly immobilized on the sensor chip CM7 surface through amine coupling reaction. The results demonstrated that peptide TNTHCDR3 was determined as TNT binding peptide and no nonspecific binding was observed. The selectivity of TNT binding peptide TNTHCDR3 was also testified by six kinds of TNT analogues. The results indicated the specific binding between TNT and peptide TNTHCDR3. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:279 / 284
页数:6
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