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细菌视紫红质光循环过程中视网膜席夫碱与Asp85和Asp96的连接性:局部可及模型

Connectivity of the retinal Schiff base to Asp85 and Asp96 during the bacteriorhodopsin photocycle: the local-access model.

作者信息

Brown L S, Dioumaev A K, Needleman R, Lanyi J K

机构信息

Department of Physiology and Biophysics, University of California, Irvine 92697, USA.

出版信息

Biophys J. 1998 Sep;75(3):1455-65. doi: 10.1016/S0006-3495(98)74064-0.

Abstract

In the recently proposed local-access model for proton transfers in the bacteriorhodopsin transport cycle (Brown et al. 1998. Biochemistry. 37:3982-3993), connection between the retinal Schiff base and Asp85 (in the extracellular direction) and Asp96 (in the cytoplasmic direction)is maintained as long as the retinal is in its photoisomerized state. The directionality of the proton translocation is determined by influences in the protein that make Asp85 a proton acceptor and, subsequently, Asp96 a proton donor. The idea of concurrent local access of the Schiff base in the two directions is now put to a test in the photocycle of the D115N/D96N mutant. The kinetics had suggested that there is a single sequence of intermediates, L<-->M1<-->M2<-->N, and the M2-->M1 reaction depends on whether a proton is released to the extracellular surface. This is now confirmed. We find that at pH 5, where proton release does not occur, but not at higher pH, the photostationary state created by illumination with yellow light contains not only the M1 and M2 states, but also the L and the N intermediates. Because the L and M1 states decay rapidly, they can be present only if they are in equilibrium with later intermediates of the photocycle. Perturbation of this mixture with a blue flash caused depletion of the M intermediate, followed by its partial recovery at the expense of the L state. The change in the amplitude of the C=O stretch band at 1759 cm-1 demonstrated protonation of Asp85 in this process. Thus, during the reequilibration the Schiff base lost its proton to Asp85. Because the N state, also present in the mixture, arises by protonation of the Schiff base from the cytoplasmic surface, these results fulfill the expectation that under the conditions tested the extracellular access of the Schiff base would not be lost at the time when there is access in the cytoplasmic direction. Instead, the connectivity of the Schiff base flickers rapidly (with the time constant of the M1<-->M2 equilibration) between the two directions during the entire L-to-N segment of the photocycle.

摘要

在最近提出的细菌视紫红质转运循环中质子转移的局部通道模型中(Brown等人,1998年。《生物化学》。37:3982 - 3993),只要视黄醛处于光异构化状态,视黄醛席夫碱与Asp85(在细胞外方向)和Asp96(在细胞质方向)之间的连接就得以维持。质子转运的方向性由蛋白质中的影响因素决定,这些因素使Asp85成为质子受体,随后使Asp96成为质子供体。现在,在D115N/D96N突变体的光循环中对席夫碱在两个方向上同时存在局部通道这一观点进行了测试。动力学研究表明存在单一的中间体序列,即L<-->M1<-->M2<-->N,并且M2-->M1反应取决于质子是否释放到细胞外表面。现在这一点得到了证实。我们发现,在pH 5时,质子不会释放,但在较高pH时则会释放,用黄光照射产生的光稳态不仅包含M1和M2状态,还包含L和N中间体。由于L和M1状态迅速衰减,只有当它们与光循环的后续中间体处于平衡时才会存在。用蓝光闪光扰动这种混合物会导致M中间体减少,随后以L状态为代价部分恢复。1759 cm-1处C = O伸缩带振幅的变化表明在此过程中Asp85发生了质子化。因此,在重新平衡过程中,席夫碱将质子转移给了Asp85。由于混合物中也存在的N状态是由细胞质表面的席夫碱质子化产生的,这些结果符合预期,即在测试条件下,当存在细胞质方向的通道时,席夫碱的细胞外通道不会丧失。相反,在光循环的整个L到N阶段,席夫碱在两个方向之间快速闪烁(以M1<-->M2平衡的时间常数)。

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