| Literature DB >> 31922395 |
Yasushi Kanai1, Yuki Ohmuro-Matsuyama2, Masami Tanioku1, Shota Ushiba3, Takao Ono1, Koichi Inoue1, Tetsuya Kitaguchi2, Masahiko Kimura3, Hiroshi Ueda2, Kazuhiko Matsumoto1.
Abstract
Due to its high carrier mobility, graphene is considered a suitable material for use in field-effect transistors. However, its application to immunosensing of small molecules is still elusive. To investigate the potential of graphene field effect transistors (G-FET) as a sensor for small molecules with small or no charge, we applied the open-sandwich immunoassay (OS-IA), which detects low-molecular-weight antigens noncompetitively, to G-FET. Using an antibody variable fragment VL immobilized on graphene and a hyperacidic region of amyloid precursor protein fused to the other variable fragment VH, we successfully detected a small antigen peptide consisting of 7 amino acids (BGP-C7), with a more than 100-fold increase in sensitivity compared with that measured by enzyme-linked OS-IA. Furthermore, we succeeded in detecting BGP-C7 in the presence of human serum with similar sensitivity, suggesting its potential application in clinical diagnostics.Entities:
Keywords: amyloid precursor protein; antibody variable region; clinical diagnostics; electrochemical biosensor; fusion protein; graphene; immunosensor
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Year: 2020 PMID: 31922395 DOI: 10.1021/acssensors.9b02137
Source DB: PubMed Journal: ACS Sens ISSN: 2379-3694 Impact factor: 7.711