TY - JOUR
T1 - Target-protein-selective inactivation and labelling using an oxidative catalyst
AU - Sato, Shinichi
AU - Tsushima, Michihiko
AU - Nakamura, Hiroyuki
N1 - Funding Information:
This work was partially supported by Grants-in-Aid for 'Grant-in-Aid for Young Scientists (A) (15H05490 to S. Sato)' and 'Chemistry for Multimolecular Crowding Biosystems (18H04542 to H. Nakamura)' from the MEXT, Japan.
Publisher Copyright:
© 2018 The Royal Society of Chemistry.
PY - 2018
Y1 - 2018
N2 - Reactive oxygen species (ROS) and radical species generated using oxidative single-electron transfer (SET) catalysts are highly reactive, inducing local environmental oxidative reactions, resulting in protein inactivation and labelling in proximity to the catalysts. Oxidative catalysts bound to the target protein generate ROS which induce oxidation only within a limited radius (∼30 nm), resulting in target-protein-selective inactivation. On the other hand, protein chemical labelling reactions via ROS or SET induced by the catalysts are completed in proximity to the catalyst. These proximity labelling techniques have recently attracted considerable attention as innovative tools to elucidate protein interaction mapping and unknown protein-protein interaction (PPI) partners. Not only can peroxidases be genetically introduced into the protein of interest but also ligand-conjugated catalysts can catalyze oxidative SET reactions in a protein mixture under intracellular conditions. In this review, we focus on two approaches of selective inactivation of protein functions and selective protein labelling using oxidative SET catalysts.
AB - Reactive oxygen species (ROS) and radical species generated using oxidative single-electron transfer (SET) catalysts are highly reactive, inducing local environmental oxidative reactions, resulting in protein inactivation and labelling in proximity to the catalysts. Oxidative catalysts bound to the target protein generate ROS which induce oxidation only within a limited radius (∼30 nm), resulting in target-protein-selective inactivation. On the other hand, protein chemical labelling reactions via ROS or SET induced by the catalysts are completed in proximity to the catalyst. These proximity labelling techniques have recently attracted considerable attention as innovative tools to elucidate protein interaction mapping and unknown protein-protein interaction (PPI) partners. Not only can peroxidases be genetically introduced into the protein of interest but also ligand-conjugated catalysts can catalyze oxidative SET reactions in a protein mixture under intracellular conditions. In this review, we focus on two approaches of selective inactivation of protein functions and selective protein labelling using oxidative SET catalysts.
UR - http://www.scopus.com/inward/record.url?scp=85052696427&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85052696427&partnerID=8YFLogxK
U2 - 10.1039/c8ob01484a
DO - 10.1039/c8ob01484a
M3 - Review article
C2 - 30128443
AN - SCOPUS:85052696427
SN - 1477-0520
VL - 16
SP - 6168
EP - 6179
JO - Organic and Biomolecular Chemistry
JF - Organic and Biomolecular Chemistry
IS - 34
ER -