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隐藻视蛋白通道的多样性。

Diversity of Chlamydomonas channelrhodopsins.

机构信息

Center for Membrane Biology, Department of Biochemistry and Molecular Biology, University of Texas Medical School, Houston, TX, USA.

出版信息

Photochem Photobiol. 2012 Jan-Feb;88(1):119-28. doi: 10.1111/j.1751-1097.2011.01027.x. Epub 2011 Nov 29.

DOI:10.1111/j.1751-1097.2011.01027.x
PMID:22044280
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3253254/
Abstract

Channelrhodopsins act as photoreceptors for control of motility behavior in flagellates and are widely used as genetically targeted tools to optically manipulate the membrane potential of specific cell populations ("optogenetics"). The first two channelrhodopsins were obtained from the model organism Chlamydomonas reinhardtii (CrChR1 and CrChR2). By homology cloning we identified three new channelrhodopsin sequences from the same genus, CaChR1, CyChR1 and CraChR2, from C. augustae, C. yellowstonensis and C. raudensis, respectively. CaChR1 and CyChR1 were functionally expressed in HEK293 cells, where they acted as light-gated ion channels similar to CrChR1. However, both, which are similar to each other, differed from CrChR1 in current kinetics, inactivation, light intensity dependence, spectral sensitivity and dependence on the external pH. These results show that extensive channelrhodopsin diversity exists even within the same genus, Chlamydomonas. The maximal spectral sensitivity of CaChR1 was at 520 nm at pH 7.4, about 40 nm redshifted as compared to that of CrChR1 under the same conditions. CaChR1 was successfully expressed in Pichia pastoris and exhibited an absorption spectrum identical to the action spectrum of CaChR1-generated photocurrents. The redshifted spectra and the lack of fast inactivation in CaChR1- and CyChR1-generated currents are features desirable for optogenetics applications.

摘要

通道蛋白视紫红质作为鞭毛运动行为控制的光受体,被广泛用作遗传靶向工具,以光学方式操纵特定细胞群体的膜电位(“光遗传学”)。前两种通道蛋白视紫红质来自模式生物莱茵衣藻(CrChR1 和 CrChR2)。通过同源克隆,我们从同一属中鉴定出三种新的通道蛋白视紫红质序列,分别来自 C. augustae、C. yellowstonensis 和 C. raudensis 的 CaChR1、CyChR1 和 CraChR2。CaChR1 和 CyChR1 在 HEK293 细胞中表达,它们作为光门控离子通道与 CrChR1 相似。然而,这两个与 CrChR1 相似的通道蛋白在电流动力学、失活、光强依赖性、光谱敏感性和对外界 pH 值的依赖性方面存在差异。这些结果表明,即使在同一属的莱茵衣藻中,也存在广泛的通道蛋白视紫红质多样性。CaChR1 的最大光谱灵敏度在 pH 7.4 时为 520nm,与相同条件下的 CrChR1 相比,红移约 40nm。CaChR1 在毕赤酵母中成功表达,其吸收光谱与 CaChR1 产生的光电流的作用光谱相同。CaChR1 和 CyChR1 产生的电流中红移的光谱和缺乏快速失活是光遗传学应用所需的特征。

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