GFID 범부처방역연계 감연병연구개발재단

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  • 알림마당
성과공유
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  • 알림마당
  • 성과공유

Fabrication of electrochemical biosensor composed of multi-functional DNA structure/au nanospike on Micro-Gap/PCB system for detecting troponin Ⅰ in human serum

구분
방역연계범부처감염병R&D사업
저자명
Taek Lee, Yeon-Ju Lee, Sun-Yong Park, Keon-Young Hong, Young-Hun Kim, Chul-Hwan Park, Yong-Ho Chung, Min-Ho Lee, Jun-Hong Min
학술지명
Colloids and Surfaces B: Biointerfaces
발표년월
2019-03-26
작성일
2023-11-13
조회수
194

1. RFP : 다중 감염성 질환 스크리닝을 위한 멀티채널 진단키트 개발

2. 해당분과 : 4-2-1과제

3. 과제명 : 4분류 질환의 현장 동시 검출용 유전자 분석 기반

4. 연구책임자 : 임채승(고려대학교)


[Abstract]

Acute myocardial infarction (AMI) is one of the most serious diseases affecting human beings. In this study, in order to rapidly detect AMI disease, the authors fabricated a label-free electrochemical biosensor composed of a multi-functional DNA structure on Au nanospike (AuNS) with a fabricated Au micro-gap electrode which was incorporated with a PCB chip in order to detect cardiac troponin I (cTnI). As a bioprobe, the DNA 3 way-junction (3WJ) was introduced, because the DNA 3WJ has three arms for embodying the multi-functionality. Each piece of DNA was assembled to simultaneously form the DNA 3WJ for cTnI detection, signal transduction, and immobilization, respectively. The assembled DNA 3WJ structure was confirmed by Native-TBM PAGE. Moreover, in order to increase the electrochemical signal sensitivity, AuNS was prepared. The Au micro-gap array is fabricated with a printed circuit board (PCB) chip in order to control each micro-gap electrode panel selectively so as to detect low volumes of cTnI. Then, the DNA strucuture on pAuNS-modified electrode was prepared using the layer-by-layer (LbL) assembly method. FE-SEM and AFM were used to investigate the modified-surface morphology. The cyclic voltammetry (CV) was measured to confirm the cTnI binding to DNA 3WJ-modified electrode. cTnI was detected in the HEPES solution and human serum, respectively. The LOD result exhibited 1.0pM in HEPES solution and 1.0pM in 20% diluted human serum, respectively. In addition, the selectivity test was carried out with various proteins as the control experiment. The present study showed label-free, simple fabrication, and easy-to-tailor detection elements for cTnI.