Solvent-Slaved Motions in the Hydride Tunneling Reaction Catalyzed by Human Glycolate Oxidase
Solvent-Slaved Motions in the Hydride Tunneling Reaction Catalyzed by Human Glycolate Oxidase
复制标题
人乙醇酸氧化酶催化的氢化物隧道反应中的溶剂从动运动
DOI:
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发表时间:
2016
期刊:
影响因子:
--
通讯作者:
G. Gadda
中科院分区:
文献类型:
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作者:
Elvira Romero;Safieh Tork Ladani;D. Hamelberg;G. Gadda
Enzyme motions facilitate many hydride-transfer reactions involving quantum mechanical (QM) tunneling. The evidence mainly comes from the determination of kinetic isotope effects (KIEs) and their temperature dependence that have been used to reveal interesting characteristics of human glycolate oxidase (HsGOX). Previous studies have shown that HsGOX oxidizes glycolate to glyoxylate via a hydride-transfer mechanism to an enzyme-associated FMN. Here, we investigate the temperature effect on the anaerobic rate of flavin reduction (kred) for HsGOX with glycolate and [2R-2H]glycolate. While the kred values for HsGOX are temperature-dependent, their KIEs on the kred values (Dkred) do not change as the temperature is varied. This is consistent with the involvement of QM hydride tunneling in the highly optimized active site of HsGOX. We show that the enzyme motions are slaved by the fluctuations in the bulk solvent after determining the kred and Dkred for HsGOX at various solvent viscosities and constant temperat...
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影响因子:
2.9
作者:
O. Quaye;G. Lountos;F. Fan;A. Orville;G. Gadda
通讯作者:
O. Quaye;G. Lountos;F. Fan;A. Orville;G. Gadda
影响因子:
2.9
作者:
Feng, CJ;Kedia, RV;Enemark, JH
通讯作者:
Enemark, JH
影响因子:
2.9
作者:
Hammes, Gordon G.;Benkovic, Stephen J.;Hammes-Schiffer, Sharon
通讯作者:
Hammes-Schiffer, Sharon
影响因子:
15
作者:
Knapp, MJ;Rickert, K;Klinman, JP
通讯作者:
Klinman, JP
影响因子:
16.6
作者:
Klinman JP;Kohen A
通讯作者:
Kohen A