TY - JOUR
T1 - An electrochemical device for the assay of the interaction between a dioxin receptor and its various ligands
AU - Murata, Masaharu
AU - Gonda, Hatsumi
AU - Yano, Kentaro
AU - Kuroki, Shinichiro
AU - Suzutani, Tatsuo
AU - Katayama, Yoshiki
N1 - Funding Information:
This work has been supported by a grant from the New Energy and Industrial Technology Development Organization (NEDO) to M. Murata. Financial support was also provided by the Kansai Electric Power Company and a Grant-in-Aid for Scientific Research (No. 411, entitled ‘The environmental risk of endocrine disruptor’) from the Ministry of Education, Culture, Sports, Science and Technology of Japan.
PY - 2004/1/5
Y1 - 2004/1/5
N2 - Aryl hydrocarbon receptor (AhR) is a ligand-activated transcription factor that mediates the toxic and biological effects of a variety of chemicals. Although a significant amount of information is available with respect to the planar aromatic hydrocarbon AhR ligands, information on the actual spectrum of chemical structures that can bind to and activate the AhR is insufficient. In order to determine the binding affinities of chemicals to the human AhR (hAhR), we constructed an electrochemical system which carries the hAhR ligand-binding domain on the electrode surface. The recombinant hAhR ligand-binding domain that was expressed in Escherichia coli using a T7 expression system was immobilized on a gold electrode. The specificity of this biosensor based on a ligand-receptor interaction was comparable to other in vitro screening methods. The receptor-modified electrode can rapidly detect the binding of ligands to hAhR. The electrochemical measurement can be carried out within just 5 min. This electrochemical screening system is rapid, low in cost, and adaptable to high-throughput applications without sacrificing either sensitivity or selectivity.
AB - Aryl hydrocarbon receptor (AhR) is a ligand-activated transcription factor that mediates the toxic and biological effects of a variety of chemicals. Although a significant amount of information is available with respect to the planar aromatic hydrocarbon AhR ligands, information on the actual spectrum of chemical structures that can bind to and activate the AhR is insufficient. In order to determine the binding affinities of chemicals to the human AhR (hAhR), we constructed an electrochemical system which carries the hAhR ligand-binding domain on the electrode surface. The recombinant hAhR ligand-binding domain that was expressed in Escherichia coli using a T7 expression system was immobilized on a gold electrode. The specificity of this biosensor based on a ligand-receptor interaction was comparable to other in vitro screening methods. The receptor-modified electrode can rapidly detect the binding of ligands to hAhR. The electrochemical measurement can be carried out within just 5 min. This electrochemical screening system is rapid, low in cost, and adaptable to high-throughput applications without sacrificing either sensitivity or selectivity.
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U2 - 10.1016/j.bmcl.2003.10.002
DO - 10.1016/j.bmcl.2003.10.002
M3 - Article
C2 - 14684315
AN - SCOPUS:0346887169
SN - 0960-894X
VL - 14
SP - 137
EP - 141
JO - Bioorganic and Medicinal Chemistry Letters
JF - Bioorganic and Medicinal Chemistry Letters
IS - 1
ER -