Significant enhancement of direct electric communication across enzyme-electrode interface via nano-patterning of synthetic glucose dehydrogenase on spatially tunable gold nanoparticle (AuNP)-modified electrode
- Authors
- Lee, Hyeryeong; Lee, Yoo Seok; Lee, Soo Kyung; Baek, Seungwoo; Choi, In-Geol; Jang, Jae-Hyung; Chang, In Seop
- Issue Date
- 1-2월-2019
- Publisher
- ELSEVIER ADVANCED TECHNOLOGY
- Keywords
- Direct electron transfer; Enzyme nano-patterning; Immobilization; Protein agglomeration; Charge transfer resistance
- Citation
- BIOSENSORS & BIOELECTRONICS, v.126, pp.170 - 177
- Indexed
- SCIE
SCOPUS
- Journal Title
- BIOSENSORS & BIOELECTRONICS
- Volume
- 126
- Start Page
- 170
- End Page
- 177
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/67685
- DOI
- 10.1016/j.bios.2018.10.013
- ISSN
- 0956-5663
- Abstract
- In this study, the effect of inter-enzyme steric hindrance that occurs during enzyme immobilization on the electrode, on direct electrical communications of enzyme with electrode was investigated via nano-patterning of enzymes on the electrode. Here, the nano-patterning of enzymes was achieved through the combination of DET-capable enzyme that was produced via fusion of site-specific gold binding peptide (GBP) to catalytic subunit of enzyme and gold nanoparticle (AuNP) array with highly tunable dimensions of AuNPs, resulting in spatially controllable enzyme-electrode. The nano-scale spatial control between immobilized enzymes on the highly tuned AuNPs shows different DET efficiency across the enzyme-electrode interface, showing 18.47% of maximum electron recovery which is 3.2-fold enhanced electron recovery efficiency compared to spatially non-controlled enzymes on the electrode where showed 5.7% of electron recovery. The result affirms that inter enzyme interaction is a significant parameter that decides the enzyme-electrode performance.
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Collections - Graduate School > Department of Biotechnology > 1. Journal Articles
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