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细菌视紫红质酸蓝和酸紫形式的光电压动力学:无净电荷转移的证据。

Photovoltage kinetics of the acid-blue and acid-purple forms of bacteriorhodopsin: evidence for no net charge transfer.

作者信息

Moltke S, Heyn M P

机构信息

Department of Physics, Freie Universität Berlin, Germany.

出版信息

Biophys J. 1995 Nov;69(5):2066-73. doi: 10.1016/S0006-3495(95)80077-9.

Abstract

Time-resolved photovoltage measurements were performed with the acid-blue (bR605A) and acid-purple (bR565A) forms of bacteriorhodopsin (bR) in the time range from 25 ns to 100 s. The bR605A and bR565A pigments were formed by titration with H2SO4 in the absence and presence of 150 mM KCI, respectively. Qualitatively the kinetics of the charge displacement in these two states are similar and consist of two fast phases in one direction (100 ns bandwidth limited and approximately 1 microsecond) followed by a decay in the opposite direction via one component for bR605A (4.4 +/- 0.6 ms) or two components for bR565A (33 +/- 8 microseconds and 3.6 +/- 0.5 ms). The transient photovoltage signal returns exactly to the initial value after several milliseconds, well before the passive discharge of the electrical measuring system at 2 s. We conclude that no net charge transfer occurs in either bR605A or bR565A. The direction of the fast components is opposite that of net proton translocation in bR at pH 7. So, if the charge that moves back and forth is due to a proton, it moves first in the direction of the cytoplasmic side of the membrane (< 1 microsecond) and returns to its initial position via the 4.4 ms (bR605A) or the 33 microseconds and 3.6 ms (bR565A) decay components. The amplitude of the charge motion in both low pH forms is too large to be due to isomerization alone and is comparable to one of the major components in bR at pH 7.2

摘要

在25纳秒至100秒的时间范围内,对细菌视紫红质(bR)的酸蓝(bR605A)和酸紫(bR565A)形式进行了时间分辨光电压测量。bR605A和bR565A色素分别通过在不存在和存在150 mM KCl的情况下用H2SO4滴定形成。定性地说,这两种状态下电荷位移的动力学是相似的,包括一个方向上的两个快速阶段(100纳秒带宽限制且约为1微秒),随后bR605A通过一个成分(4.4±0.6毫秒)或bR565A通过两个成分(33±8微秒和3.6±0.5毫秒)在相反方向上衰减。瞬态光电压信号在几毫秒后精确地回到初始值,远早于2秒时电测量系统的被动放电。我们得出结论,在bR605A或bR565A中都没有发生净电荷转移。快速成分的方向与pH 7时bR中净质子转运的方向相反。因此,如果来回移动的电荷是由于质子引起的,它首先朝着膜的细胞质侧方向移动(<1微秒),并通过4.4毫秒(bR605A)或33微秒和3.6毫秒(bR565A)的衰减成分回到其初始位置。两种低pH形式中电荷运动的幅度太大,不可能仅由异构化引起,并且与pH 7.2时bR中的一个主要成分相当。

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