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牛肉心线粒体嵴膜中细胞色素b和泛醌的组织与功能

Organization and function of cytochrome b and ubiquinone in the cristae membrane of beef heart mitochondria.

作者信息

von Jagow G, Link T A, Ohnishi T

出版信息

J Bioenerg Biomembr. 1986 Jun;18(3):157-79. doi: 10.1007/BF00743462.

Abstract

The arrangement and function of the redox centers of the mammalian bc1 complex is described on the basis of structural data derived from amino acid sequence studies and secondary structure predictions and on the basis of functional studies (i.e., EPR data, inhibitor studies, and kinetic experiments). Two ubiquinone reaction centers do exist--a QH2 oxidation center situated at the outer, cytosolic surface of the cristae membrane (Q0 center), and a Q reduction center (Qi center) situated more to the inner surface of the cristae membrane. The Q0 center is formed by the b-566 domain of cytochrome b, the FeS protein, and maybe an additional small subunit, whereas the Qi center is formed by the b-562 domain of cytochrome b and presumably the 13.4 kDa protein ("QP-C"). The "Q binding proteins" are proposed to be protein subunits of the Q reaction centers of various multiprotein complexes. The path of electron flow branches at the Q0 center, half of the electrons flowing via the high-potential cytochrome chain to oxygen and half of the electrons cycling back into the Q pool via the cytochrome b path connecting the two Q reaction centers. During oxidation of QH2, 2H+ are released to the cytosolic space and during reduction of Q, 2H+ are taken up from the matrix side, resulting in a net transport across the membrane of 2H+ per e- flown from QH2 to cytochrome c, the H+ being transported across the membrane as H (H+ + e-) by the mobile carrier Q. The authors correct their earlier view of cytochrome b functioning as a H+ pump, proposing that the redox-linked pK changes of the acidic groups of cytochrome b are involved in the protonation/deprotonation processes taking place during the reduction and oxidation of Q. The reviewers stress that cytochrome b is in equilibrium with the Q pool via the Qi center, but not via the Q0 center. Their view of the mechanisms taking place at the reductase is a Q cycle linked to a Q-pool where cytochrome b is acting as an electron pump.

摘要

基于氨基酸序列研究和二级结构预测得出的结构数据以及功能研究(即电子顺磁共振数据、抑制剂研究和动力学实验),对哺乳动物bc1复合物氧化还原中心的排列和功能进行了描述。确实存在两个泛醌反应中心——一个位于嵴膜外侧胞质表面的QH2氧化中心(Q0中心),以及一个更靠近嵴膜内表面的Q还原中心(Qi中心)。Q0中心由细胞色素b的b - 566结构域、铁硫蛋白以及可能的另一个小亚基形成,而Qi中心由细胞色素b的b - 562结构域以及大概13.4 kDa的蛋白质(“QP - C”)形成。“Q结合蛋白”被认为是各种多蛋白复合物Q反应中心的蛋白质亚基。电子流路径在Q0中心分支,一半电子经高电位细胞色素链流向氧气,另一半电子经连接两个Q反应中心的细胞色素b路径循环回到Q池。在QH2氧化过程中,2个H⁺释放到胞质空间,在Q还原过程中,2个H⁺从基质侧摄取,导致每从QH2流向细胞色素c一个电子,就有2个H⁺跨膜净转运,H⁺通过移动载体Q以H(H⁺ + e⁻)的形式跨膜转运。作者修正了他们早期关于细胞色素b作为H⁺泵起作用的观点,提出细胞色素b酸性基团的氧化还原相关pK变化参与了Q还原和氧化过程中发生的质子化/去质子化过程。审稿人强调细胞色素b通过Qi中心与Q池处于平衡状态,但不是通过Q0中心。他们对还原酶处发生机制的观点是与Q池相连的Q循环,其中细胞色素b作为电子泵起作用。

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