Rapid Colorimetric Antibody Detection Using a Dual-function Peptide Probe for Silver Nanoparticle Aggregation and Antibody Recognition

被引:10
作者
Okochi, Mina [1 ,2 ]
Kamiya, Tomohiro [1 ]
Omasa, Takeshi [3 ]
Tanaka, Masayoshi [2 ]
Honda, Hiroyuki [1 ]
机构
[1] Nagoya Univ, Sch Engn, Dept Biotechnol, Chikusa Ku, Furo Cho, Nagoya, Aichi 4648603, Japan
[2] Tokyo Inst Technol, Grad Sch Sci & Engn, Dept Chem Engn, Meguro Ku, 2-12-1-S1-24 O Okayama, Tokyo 1528552, Japan
[3] Osaka Univ, Grad Sch Engn, Dept Mat & Life Sci, 2-1 Yamadaoka, Suita, Osaka 5650871, Japan
关键词
Peptide; silver nanoparticle; label-free colorimetric assay; antibody detection; UNMODIFIED GOLD NANOPARTICLES; NONCROSSLINKING AGGREGATION; SPOT SYNTHESIS; ASSAY; DESIGN; ARRAYS; IDENTIFICATION; AFFINITY; IONS;
D O I
10.2116/analsci.32.93
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Simple and rapid tools for antibody detection are beneficial for therapeutic monoclonal antibody development. Using a synthetic cationic antibody-recognizing peptide, a label-free colorimetric assay for antibody detection was established, in which a solution containing silver nanoparticles (AgNPs) changes color depending on particle aggregation/dispersion. Among the peptide probes we previously screened as IgG binding, one (NKFRGKYK) has four cationic amino acids and a pI of 10.46. Hence, we hypothesized that the peptide would both bind IgG and induce anionic AgNP aggregation via electrostatic interactions. This dual functionality of the IgG binding peptide could be useful for colorimetric detection. The detection of IgG in a solution containing culture media was investigated, and IgG was successfully detected at 100 to 500 nM within 2 min. This method is promising for high-throughput selection of IgG-producing cells since it is fast, readily observable, and does not involve complicated nanoparticle functionalization.
引用
收藏
页码:93 / 97
页数:5
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