| Literature DB >> 27636559 |
Lin Zhou1, Hongju Mao2, Chunyan Wu3, Lin Tang4, Zhenhua Wu1, Hao Sun5, Honglian Zhang5, Hongbo Zhou5, Chunping Jia5, Qinghui Jin5, Xianfeng Chen6, Jianlong Zhao7.
Abstract
A label-free immunosensor based on antibody-modified graphene field effect transistor (GFET) was presented. Antibodies targeting carcinoembryonic antigen (Anti-CEA) were immobilized to the graphene surface via non-covalent modification. The bifunctional molecule, 1-pyrenebutanoic acid succinimidyl ester, which is composed of a pyrene and a reactive succinimide ester group, interacts with graphene non-covalently via π-stacking. The succinimide ester group reacts with the amine group to initiate antibody surface immobilization, which was confirmed by X-ray Photoelectron Spectroscopy, Atomic Force Microscopy and Electrochemical Impedance Spectroscopy. The resulting anti-CEA modified GFET sufficiently monitored the reaction between CEA protein and anti-CEA in real-time with high specificity, which revealed selective electrical detection of CEA with a limit of detection (LOD) of less than 100pg/ml. The dissociation constant between CEA protein and anti-CEA was estimated to be 6.35×10-11M, indicating the high affinity and sensitivity of anti-CEA-GFET. Taken together, the graphene biosensors provide an effective tool for clinical application and point-of-care medical diagnostics. Copyright ÂEntities:
Keywords: CEA protein; Dissociation constant; Graphene; Non-covalent modification
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Year: 2016 PMID: 27636559 DOI: 10.1016/j.bios.2016.09.025
Source DB: PubMed Journal: Biosens Bioelectron ISSN: 0956-5663 Impact factor: 10.618