Modulation of the kinetics and the steady-state level of intermediates of mitochondrial coupled reactions by inhibitors and uncouplers.
Modulation of the kinetics and the steady-state level of intermediates of mitochondrial coupled reactions by inhibitors and uncouplers.
复制标题
通过抑制剂和解偶联剂调节线粒体偶联反应的动力学和中间体的稳态水平。
DOI:
10.1021/bi00300a035
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发表时间:
1984
期刊:
影响因子:
2.9
通讯作者:
Hatefi,Y
中科院分区:
文献类型:
--
作者:
Yagi,T;Matsuno-Yagi,A;Vik,SB;Hatefi,Y
Takao Yagi, Akemi Matsuno-Yagi, Steven B. Vik,* and Youssef Hatefi* abstract:(1) In oxidative phosphorylation and ATP-driven uphill electron transfer from succinate to NAD, double-reciprocal plots of rates vs. substrate concentrations of the en-ergy-driven reactions are a family of parallel linesat several fixed subsaturating concentrations of the substrates or at several moderate concentrations of the inhibitorsof the en-ergy-yielding reactions. Thus, as shown elsewhere [Hatefi, Y., Yagi, T., Phelps, D. C „Wong, S.-Y „Vik, S. B., & Galante, YM (1982) Proc. Natl. Acad. Sci. USA 79, 1756-1760], partial uncoupling decreases the V $£ x and in-creases the K%¡ 9 of the substrates of the energy-driven reac-tions, resulting in a decrease of X/Km as a function of increased uncoupling. However, partial limitation of the flow rates of the energy-yielding reactions decreases both the V^ l% and the K^ 99 of the substrates of the energy-driven reactions, resulting in no change in V „„IK „. This is true as long as the rate limitation is moderate (eg,< 60%), under which con-ditions the steady-state membrane potential () remains essentially unchanged. At high inhibition of the energy-yielding reactions, or at moderate inhibition inthe presence of low levels of an uncoupler to cause partial uncoupling, then the family of double-reciprocal plots is no longer parallel and tends to converge toward the left. Under these conditions, steady-state and VmiJKm also decrease as inhibition is increased.(2) The relationship between the magnitude of steady-state and the rate of the energy-driven reaction was studied in oxidative phosphorylation, ATP-driven electron transfer from succinate to NAD, and respiration-driven uniport