Inaguma Asumi, Tsukamoto Hisao, Kato Hideaki E, Kimura Tetsunari, Ishizuka Toru, Oishi Satomi, Yawo Hiromu, Nureki Osamu, Furutani Yuji
From the Department of Life and Coordination-Complex Molecular Science, Institute for Molecular Science, 38 Nishigo-Naka, Myodaiji, Okazaki 444-8585, Japan, PRESTO, Japan Science and Technology Agency (JST), 4-1-8 Honcho Kawaguchi, Saitama 332-0012, Japan, Department of Structural Molecular Science, Graduate University for Advanced Studies (SOKENDAI), 38 Nishigo-Naka, Myodaiji, Okazaki 444-8585, Japan.
From the Department of Life and Coordination-Complex Molecular Science, Institute for Molecular Science, 38 Nishigo-Naka, Myodaiji, Okazaki 444-8585, Japan, Department of Structural Molecular Science, Graduate University for Advanced Studies (SOKENDAI), 38 Nishigo-Naka, Myodaiji, Okazaki 444-8585, Japan.
J Biol Chem. 2015 May 1;290(18):11623-34. doi: 10.1074/jbc.M115.642256. Epub 2015 Mar 21.
Channelrhodopsin-2 (ChR2) from the green alga Chlamydomonas reinhardtii functions as a light-gated cation channel that has been developed as an optogenetic tool to stimulate specific nerve cells in animals and control their behavior by illumination. The molecular mechanism of ChR2 has been extensively studied by a variety of spectroscopic methods, including light-induced difference Fourier transform infrared (FTIR) spectroscopy, which is sensitive to structural changes in the protein upon light activation. An atomic structure of channelrhodopsin was recently determined by x-ray crystallography using a chimera of channelrhodopsin-1 (ChR1) and ChR2. Electrophysiological studies have shown that ChR1/ChR2 chimeras are less desensitized upon continuous illumination than native ChR2, implying that there are some structural differences between ChR2 and chimeras. In this study, we applied light-induced difference FTIR spectroscopy to ChR2 and ChR1/ChR2 chimeras to determine the molecular basis underlying these functional differences. Upon continuous illumination, ChR1/ChR2 chimeras exhibited structural changes distinct from those in ChR2. In particular, the protonation state of a glutamate residue, Glu-129 (Glu-90 in ChR2 numbering), in the ChR chimeras is not changed as dramatically as in ChR2. Moreover, using mutants stabilizing particular photointermediates as well as time-resolved measurements, we identified some differences between the major photointermediates of ChR2 and ChR1/ChR2 chimeras. Taken together, our data indicate that the gating and desensitizing processes in ChR1/ChR2 chimeras are different from those in ChR2 and that these differences should be considered in the rational design of new optogenetic tools based on channelrhodopsins.
来自莱茵衣藻的通道视紫红质-2(ChR2)作为一种光门控阳离子通道发挥作用,它已被开发成为一种光遗传学工具,用于刺激动物体内特定的神经细胞,并通过光照来控制其行为。ChR2的分子机制已通过多种光谱方法进行了广泛研究,包括光诱导差分傅里叶变换红外(FTIR)光谱,该方法对光激活后蛋白质的结构变化敏感。最近,通过X射线晶体学使用通道视紫红质-1(ChR1)和ChR2的嵌合体确定了通道视紫红质的原子结构。电生理研究表明,ChR1/ChR2嵌合体在持续光照下比天然ChR2脱敏程度更低,这意味着ChR2与嵌合体之间存在一些结构差异。在本研究中,我们将光诱导差分FTIR光谱应用于ChR2和ChR1/ChR2嵌合体,以确定这些功能差异背后的分子基础。在持续光照下,ChR1/ChR2嵌合体表现出与ChR2不同的结构变化。特别是,ChR嵌合体中谷氨酸残基Glu-129(按照ChR2编号为Glu-90)的质子化状态变化不如ChR2中那么显著。此外,我们使用稳定特定光中间体的突变体以及时间分辨测量,确定了ChR2和ChR1/ChR2嵌合体主要光中间体之间的一些差异。综上所述,我们的数据表明,ChR1/ChR2嵌合体中的门控和脱敏过程与ChR2中的不同,在基于通道视紫红质的新型光遗传学工具的合理设计中应考虑这些差异。