期刊
BIOSENSORS & BIOELECTRONICS
卷 27, 期 1, 页码 167-171出版社
ELSEVIER ADVANCED TECHNOLOGY
DOI: 10.1016/j.bios.2011.06.037
关键词
Nanobelt; Fluorescence; FRET; DNA detection; Single-base mismatch
类别
资金
- National Basic Research Program of China [2011CB935800]
In this article, we report on the first use of fluorescence resonance energy transfer (FRET) dye-labeled probe for fluorescence resonance enhanced DNA detection to greatly improve discrimination ability toward single-base mismatch using conjugation polymer poly(p-phenylenediamine) nanobelts (PNs) as a sensing platform. The suggested FRET dye-labeled probe contains a 5-carboxyfluorescein (FAM) group at 5' end of the oligomer as a donor and a 6-carboxy-X-rhodamine (ROX) attached to a modified cytosine (C) base as an acceptor, which were separated by three bases. The general concept used in this DNA assay is based on adsorption of the FRET dye-labeled single-stranded DNA (ssDNA) probe by PN, which is accompanied by substantial fluorescence quenching and disappearance of FRET. The subsequent specific hybridization with its target forms a double-stranded DNA (dsDNA), resulting in desorption of the hybridized duplex from PN surface accompanied by reoccurrence of FRET and fluorescence recovery. It suggests that the discrimination ability of this FRET probe based system toward single-base mismatch is about 5.2 times that of the system based on single dye-labeled probe based system. (C) 2011 Elsevier B.V. All rights reserved.
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