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Label-free and high-sensitive detection of Kirsten rat sarcoma viral oncogene homolog and epidermal growth factor receptor mutation using Kelvin probe force microscopy

Authors
Jang, KuewhanChoi, JaeyeongPark, ChanhoNa, Sungsoo
Issue Date
15-1월-2017
Publisher
ELSEVIER ADVANCED TECHNOLOGY
Keywords
Epidermal growth factor receptor (EGFR); Kirsten rat sarcoma viral oncogene homolog (KRAS); Kelvin probe force microscopy (KPFM); Detection; DNA; Gold nanoparticle (AuNP)
Citation
BIOSENSORS & BIOELECTRONICS, v.87, pp.222 - 228
Indexed
SCIE
SCOPUS
Journal Title
BIOSENSORS & BIOELECTRONICS
Volume
87
Start Page
222
End Page
228
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/84914
DOI
10.1016/j.bios.2016.08.045
ISSN
0956-5663
Abstract
Assessment of Kirsten rat sarcoma viral oncogene homolog (KRAS) and epidermal growth factor receptor (EGFR) mutations are essential for targeted therapies of patients with non small cell lung cancer. In this report, we propose a label-free and high-sensitive detection method of KRAS and EGFR mutations using KPFM and a gold nanoparticle (AuNP) based platform that densely adsorbs probe DNA and minimizes the sensing area. The detection is based on the evaluation of the surface potential of each AuNP. When AuNPs are modified with probe DNA (AuNP pDNA), the surface potential is shifted towards the negative potential due to the negatively charged DNA backbone. When AuNP pDNA further captures target mutant DNA through DNA hybridization, an additional surface potential shift occurs. The platform is able to detect KRAS mutant DNA (13 mer) and EGFR mutant DNA (84 mer) with a limit of detection (LOD) of 3.3 pM. Furthermore, the platform is able to detect selectively the KRAS mutant DNA from its wild-type DNA. Our proposed label-free and high-sensitive KPFM method has shown potential glimpses of a personalized medical diagnosis for cancer patients. (C) 2016 Elsevier B.V. All rights reserved.
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공과대학 (기계공학부)
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