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Ultrasensitive FRET-based DNA sensor using PNA/DNA hybridization

Authors
Yang, Lan-HeeAhn, Dong JuneKoo, Eunhae
Issue Date
1-12월-2016
Publisher
ELSEVIER SCIENCE BV
Keywords
Fret; QD; DNA sensor; Microcapillary; PNA
Citation
MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS, v.69, pp.625 - 630
Indexed
SCIE
SCOPUS
Journal Title
MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS
Volume
69
Start Page
625
End Page
630
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/86578
DOI
10.1016/j.msec.2016.07.021
ISSN
0928-4931
Abstract
In the diagnosis of genetic diseases, rapid and highly sensitive DNA detection is crucial. Therefore, many strategies for detecting target DNA have been developed, including electrical, optical, and mechanical methods. Herein, a highly sensitive FRET based sensor was developed by using PNA (Peptide Nucleic Acid) probe and QD, in which red color QDs are hybridized with capture probes, reporter probes and target DNAs by EDC-NHS coupling. The hybridized probe with target DNA gives off fluorescent signal due to the energy transfer from QD to Cy5 dye in the reporter probe. Compared to the conventional DNA sensor using DNA probes, the DNA sensor using PNA probes shows higher FRET factor and efficiency due to the higher reactivity between PNA and target DNA. In addition, to elicit the effect of the distance between the donor and the acceptor, we have investigated two types of the reporter probes having Cy5 dyes attached at the different positions of the reporter probes. Results show that the shorter the distance between QDs and Cy5s, the stronger the signal intensity. Furthermore, based on the fluorescence microscopy images using microcapillary chips, the FRET signal is enhanced to be up to 276% times stronger than the signal obtained using the cuvette by the fluorescence spectrometer. These results suggest that the PNA probe system conjugated with QDs can be used as ultrasensitive DNA nanosensors. (C) 2016 Published by Elsevier B.V.
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공과대학 (화공생명공학과)
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