Aromatic Lipophilic Spin Traps Effectively Inhibit RPE65 Isomerohydrolase Activity
Year: 2011
Type: article
Abstract: We previously showed that RPE65 does not specifically produce 11-cis-retinol only but also 13-cis-retinol, supporting a carbocation or radical cation mechanism of isomerization. The intrinsic properties of conjugated polyene chains result in facile formation of radical cations in oxidative conditions. We hypothesized that such radical intermediates, if involved in the mechanism of RPE65, could be stabilized by spin traps. We tested a variety of hydrophilic and lipophilic spin traps for their ability to inhibit RPE65 isomerohydrolase activity. We found that the aromatic lipophilic spin traps such as N-tert-butyl-α-phenylnitrone (PBN), 2,2-dimethyl-4-phenyl-2H-imidazole-1-oxide (DMPIO), and nitrosobenzene (NB) strongly inhibit RPE65 isomerohydrolase activity in vitro.
Source: Biochemistry
DOI: 10.1021/bi200532m
Authors: Eugenia Poliakov, Toral Parikh, Michael Ayele, Stephanie Kuo, Preethi Chander, Susan Gentleman, T. Michael Redmond
Institutions: National Institutes of Health, National Eye Institute
Language: English
Subfield: Spectroscopy
Field: Chemistry
Domain: Physical Sciences
Open Access status: green
OpenAlex ID: W2025323356
