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细菌视紫红质光循环中细胞质表面质子摄取与视黄醛再异构化的关系:理解pH变化以及N和O中间体复杂动力学的尝试。

Relationship of proton uptake on the cytoplasmic surface and reisomerization of the retinal in the bacteriorhodopsin photocycle: an attempt to understand the complex kinetics of the pH changes and the N and O intermediates.

作者信息

Cao Y, Brown L S, Needleman R, Lanyi J K

机构信息

Department of Physiology and Biophysics, University of California, Irvine 92717.

出版信息

Biochemistry. 1993 Sep 28;32(38):10239-48. doi: 10.1021/bi00089a046.

Abstract

In the bacteriorhodopsin photocycle the recovery of the initial BR state from the M intermediate occurs via the N and O intermediates. The molecular events in this process include reprotonation of the Schiff base and the subsequent uptake of a proton from the cytoplasmic side, as well as reisomerization of the retinal from 13-cis to all-trans. We have studied the kinetics of the intermediates and the proton uptake. At moderately low pH little of the N state accumulates, and the O state dominates in the reactions that lead from M to BR. The proton uptake lags behind the formation of O, suggesting the sequence N(0)<==>O(0) + H+ (from the bulk)-->O(+1)-->BR+H+ (to the bulk), where the superscripts indicate the net protonation state of the protein relative to BR. Together with a parallel study of ours at moderately high pH, these results suggest that the sequence of proton uptake and retinal reisomerization depends on pH: at low pH the isomerization occurs first and O accumulates, but at high pH the isomerization is delayed and therefore N accumulates. Although this model contains too many rate constants for rigorous testing, we find that it will generate most of the characteristic pH-dependent kinetic features of the photocycle with few assumptions other than pH dependency for protonation at the proton release and uptake steps.

摘要

在细菌视紫红质光循环中,从M中间体恢复到初始BR状态是通过N和O中间体进行的。这个过程中的分子事件包括席夫碱的再质子化以及随后从细胞质侧摄取一个质子,还有视黄醛从13-顺式异构化为全反式。我们研究了中间体的动力学和质子摄取。在适度低pH值下,几乎没有N状态积累,并且在从M到BR的反应中O状态占主导。质子摄取滞后于O的形成,这表明反应顺序为N(0)<==>O(0) + H+(来自本体)-->O(+1)-->BR + H+(到本体),其中上标表示蛋白质相对于BR的净质子化状态。连同我们在适度高pH值下的平行研究,这些结果表明质子摄取和视黄醛异构化的顺序取决于pH值:在低pH值下,异构化首先发生且O积累,但在高pH值下,异构化延迟,因此N积累。尽管这个模型包含太多速率常数难以进行严格测试,但我们发现它将产生光循环中大多数特征性的pH依赖性动力学特征,除了在质子释放和摄取步骤中质子化的pH依赖性外几乎不需要其他假设。

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