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细菌视紫红质在480纳米和570纳米形式之间质子释放活性的可逆抑制以及麻醉诱导的酸碱平衡。

Reversible inhibition of proton release activity and the anesthetic-induced acid-base equilibrium between the 480 and 570 nm forms of bacteriorhodopsin.

作者信息

Boucher F, Taneva S G, Elouatik S, Déry M, Messaoudi S, Harvey-Girard E, Beaudoin N

机构信息

Departement de Chimie-Biologie, Université du Québec à Trois-Rivières, Canada.

出版信息

Biophys J. 1996 Feb;70(2):948-61. doi: 10.1016/S0006-3495(96)79638-8.

Abstract

In purple membrane added with general anesthetics, there exists an acid-base equilibrium between two spectral forms of the pigment: bR570 and bR480 (apparent pKa = 7.3). As the purple 570 nm bacteriorhodopsin is reversibly transformed into its red 480 nm form, the proton pumping capability of the pigment reversibly decreases, as indicated by transient proton release measurements and proton translocation action spectra of mixture of both spectral forms. It happens in spite of a complete photochemical activity in bR480 that is mostly characterized by fast deprotonation and slow reprotonation steps and which, under continuous illumination, bleaches with a yield comparable to that of bR570. This modified photochemical activity has a correlated specific photoelectrical counterpart: a faster proton extrusion current and a slower reprotonation current. The relative areas of all photocurrent phases are reduced in bR480, most likely because its photochemistry is accompanied by charge movements for shorter distances than in the native pigment, reflecting a reversible inhibition of the pumping activity.

摘要

在添加了全身麻醉剂的紫膜中,色素的两种光谱形式:bR570和bR480之间存在酸碱平衡(表观pKa = 7.3)。正如紫色的570 nm细菌视紫红质可逆地转变为其红色的480 nm形式一样,色素的质子泵浦能力也可逆地降低,这由两种光谱形式混合物的瞬态质子释放测量和质子转运作用光谱表明。尽管bR480具有完全的光化学活性,其主要特征是快速去质子化和缓慢的再质子化步骤,并且在连续光照下,其漂白产率与bR570相当,但这种情况仍会发生。这种改变的光化学活性具有相关的特定光电对应物:更快的质子外排电流和更慢的再质子化电流。bR480中所有光电流相的相对面积都减小了,最可能的原因是其光化学过程伴随着比天然色素中更短距离的电荷移动,这反映了泵浦活性的可逆抑制。

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本文引用的文献

3
pH dependence of light-induced proton release by bacteriorhodopsin.
FEBS Lett. 1993 Sep 27;331(1-2):31-4. doi: 10.1016/0014-5793(93)80291-2.
4
Decoupling of photo- and proton cycle in the Asp85-->Glu mutant of bacteriorhodopsin.
EMBO J. 1993 Oct;12(10):3721-7. doi: 10.1002/j.1460-2075.1993.tb06049.x.
8
Proton migration along the membrane surface and retarded surface to bulk transfer.
Nature. 1994 Aug 4;370(6488):379-82. doi: 10.1038/370379a0.
9
Rapid long-range proton diffusion along the surface of the purple membrane and delayed proton transfer into the bulk.
Proc Natl Acad Sci U S A. 1995 Jan 17;92(2):372-6. doi: 10.1073/pnas.92.2.372.

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