Nishikawa Taichi, Murakami Midori, Kouyama Tsutomu
Department of Physics, Graduate School of Science, Nagoya University, Nagoya 464-8602, Japan.
J Mol Biol. 2005 Sep 16;352(2):319-28. doi: 10.1016/j.jmb.2005.07.021.
The atomic structure of the trans isomer of bacteriorhodopsin was determined previously by using a 3D crystal belonging to the space group P622. Here, a structure is reported for another isomer with the 13-cis, 15-syn retinal in a dark-adapted crystal. Structural comparison of the two isomers indicates that retinal isomerization around the C13[double bond]C14 and the C15[double bond]N bonds is accompanied by noticeable displacements of a few residues in the vicinity of the retinal Schiff base and small re-arrangement of the hydrogen-bonding network in the proton release channel. On the other hand, aromatic residues surrounding the retinal polyene chain were found to scarcely move during the dark/light adaptation. This result suggests that variation in the structural rigidity within the retinal-binding pocket is one of the important factors ensuring the stereospecific isomerization of retinal.
嗜盐菌视紫红质反式异构体的原子结构先前已通过使用属于空间群P622的三维晶体得以确定。在此,报道了一种在暗适应晶体中具有13-顺式、15-顺式视黄醛的另一种异构体的结构。两种异构体的结构比较表明,围绕C13=C14和C15=N键的视黄醛异构化伴随着视黄醛席夫碱附近一些残基的明显位移以及质子释放通道中氢键网络的微小重排。另一方面,发现在暗/光适应过程中,围绕视黄醛多烯链的芳香族残基几乎没有移动。这一结果表明,视黄醛结合口袋内结构刚性的变化是确保视黄醛立体特异性异构化的重要因素之一。