TY - JOUR
T1 - Electrochemical control of bioluminescence by blocking the adsorption of the bacterial luciferase using a mercaptobipyridine self-assembled monolayer
AU - Yamasaki, Shinya
AU - Yamada, Shuto
AU - Takemura, Hiroyuki
AU - Takehara, Kô
N1 - Publisher Copyright:
© 2017, The Japan Society for Analytical Chemistry.
PY - 2017
Y1 - 2017
N2 - An N-butyl-N'-(4-mercaptobutyl)-4,4'-bipyridinium (4BMBP) was modified on a gold electrode to improve the electrochemical control of the bacterial luciferase (BL) luminescence system. The 4BMBP-modified gold electrode (4BMBP/Au) was able to prevent the adsorption of BL on the electrode surface, and enhanced the electrochemical regeneration rate of the reduced flavin mononucleotide (FMNH 2 ), which is one of the substrates of the BL luminescence reaction. By using the 4BMBP/Au, the luminescence intensity increased by about 27% compared to that of a bare gold electrode (bare Au). Moreover, the modified electrode improved the time required for analysis because the modified layer prevented BL adsorption. Even without a refreshing procedure for each measurement, a constant luminescence intensity could be observed, and the analysis time was reduced to half (about 10 min) for one sample. The 4BMBP/Au is not only useful to control of the BL luminescence system, but also for electrochemical measurements in the presence of proteins.
AB - An N-butyl-N'-(4-mercaptobutyl)-4,4'-bipyridinium (4BMBP) was modified on a gold electrode to improve the electrochemical control of the bacterial luciferase (BL) luminescence system. The 4BMBP-modified gold electrode (4BMBP/Au) was able to prevent the adsorption of BL on the electrode surface, and enhanced the electrochemical regeneration rate of the reduced flavin mononucleotide (FMNH 2 ), which is one of the substrates of the BL luminescence reaction. By using the 4BMBP/Au, the luminescence intensity increased by about 27% compared to that of a bare gold electrode (bare Au). Moreover, the modified electrode improved the time required for analysis because the modified layer prevented BL adsorption. Even without a refreshing procedure for each measurement, a constant luminescence intensity could be observed, and the analysis time was reduced to half (about 10 min) for one sample. The 4BMBP/Au is not only useful to control of the BL luminescence system, but also for electrochemical measurements in the presence of proteins.
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U2 - 10.2116/analsci.33.307
DO - 10.2116/analsci.33.307
M3 - Article
C2 - 28302971
AN - SCOPUS:85015158653
SN - 0910-6340
VL - 33
SP - 307
EP - 311
JO - Analytical Sciences
JF - Analytical Sciences
IS - 3
ER -