Slippage and uncoupling in P-type cation pumps; implications for energy transduction mechanisms and regulation of metabolism

被引:44
作者
Berman, MC [1 ]
机构
[1] Univ Cape Town, Div Chem Pathol, Fac Hlth Sci, ZA-7925 Cape Town, South Africa
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 2001年 / 1513卷 / 02期
关键词
P-type ATPase slippage; uncoupling; variable stoichiometry; channel; occluded cation; partial denaturation; heat production;
D O I
10.1016/S0005-2736(01)00356-X
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
P-type ATPases couple scalar and vectorial events under optimized states. A number of procedures and conditions lead to uncoupling or slippage. A key branching point in the catalytic cycle is at the cation-bound form of EI-P, where isomerization to E-2-P leads to coupled transport. and hydrolysis leads to uncoupled release of cations to the cis membrane surface. The phenomenon of slippage supports a channel model for active transport. Ability to occlude cations within the channel is essential for coupling. Uncoupling and slippage appear to be inherent properties of P-type cation pumps, and are significant contributors to standard metabolic rate. Heat production is favored in the uncoupled state. A number of disease conditions, include ageing, ischemia and cardiac failure, result in uncoupling of either the Ca2+-ATPase or Na+/K--ATPase. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:95 / 121
页数:27
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