IMPROVED RADIOLABELED SUBSTRATES FOR SOLUBLE EPOXIDE HYDROLASE

Citation
B. Borhan et al., IMPROVED RADIOLABELED SUBSTRATES FOR SOLUBLE EPOXIDE HYDROLASE, Analytical biochemistry, 231(1), 1995, pp. 188-200
Citations number
43
Categorie Soggetti
Biology
Journal title
ISSN journal
00032697
Volume
231
Issue
1
Year of publication
1995
Pages
188 - 200
Database
ISI
SICI code
0003-2697(1995)231:1<188:IRSFSE>2.0.ZU;2-F
Abstract
Two rapid assays for the soluble epoxide hydrolase (sEH) are described . First, a sensitive radiometric assay based on thin-layer chromatogra phy of [C-14]-cis-9,10-epoxystearic acid and its corresponding diol ([ C-14]-9,10-dihydroxystearic acid) is described. The cis fatty acid oxi de exhibits higher specific activity of hydration with sEH from mouse, rat, human, and potato compared to trans-stilbene oxide (TSO). The K- m and V-max obtained for [C-14]-cis-9,10-epoxystearic acid with mouse sEH are 11.0 mu M and 3460 nmol/min/mg protein, respectively. [C-14]-c is-9,10-Epoxystearic acid might more closely mimic the structures of n atural substrates for sEH. Second, [2-H-3]-trans-1,3-diphenylpropene o xide ([H-3]-tDPPO) and [2-H-3]-cis-1,3-diphenylpropene oxide ([H-3]-cD PPO) were synthesized and rapid radiometric assays for epoxide hydrola ses (EHs) were developed by differential partitioning of the epoxide i nto iso-octane and its corresponding diol into aqueous phase containin g methanol. It was shown that sEHs from mouse, rat, human, and potato rapidly hydrolyze [H-3]-tDPPO and in comparison to TSO have 20-, 49-, 28-, and 7-fold higher rates, respectively. Mouse sEH hydrates [H-3]-t DPPO at 26,200 nmol/min/mg protein, and a K-m of 2.80 mu M is observed . (C) 1995 Academic Press, Inc.