Catalytic site occupancy during ATP synthase catalysis

被引:68
作者
Boyer, PD [1 ]
机构
[1] Univ Calif Los Angeles, Inst Mol Biol, Los Angeles, CA 90095 USA
关键词
ATP synthase; F-1-ATPase; bi-site activation; ATP and ADP binding;
D O I
10.1016/S0014-5793(02)02293-7
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
An early proposal was that for rapid ATP synthesis by the rotational ATP synthase, a specific second site must bind ADP and P-i, and for rapid ATP hydrolysis a different second site must bind ATP. Such bi-site activation was considered to occur whether or not an ADP or ATP was at a third site. In contrast, a more recent proposal is that rapid ATP hydrolysis requires that all three sites have bound ADP or ATP present. However, discovery that one second site binds ADP better than ATP, together with other data and considerations support the earlier proposal. The retention or rebinding of ADP can explain why three sites fill during hydrolysis as ATP concentration is increased although bi-site activation still prevails. (C) 2002 Published by Elsevier Science B.V. on behalf of the Federation of European Biochemical Societies.
引用
收藏
页码:29 / 32
页数:4
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