Awasthi Mayanka, Sushmita Kumari, Kaushik Manish Singh, Ranjan Peeyush, Kateriya Suneel
Department of Cell Biology and Molecular Genetics, University of Maryland, College Park, MD 20742, USA.
Laboratory of Optobiology, School of Biotechnology, Jawaharlal Nehru University, New Delhi 110067, India.
Life (Basel). 2020 Oct 28;10(11):259. doi: 10.3390/life10110259.
Light-gated ion channel and ion pump rhodopsins are widely used as optogenetic tools and these can control the electrically excitable cells as (1) they are a single-component system i.e., their light sensing and ion-conducting functions are encoded by the 7-transmembrane domains and, (2) they show fast kinetics with small dark-thermal recovery time. In cellular signaling, a signal receptor, modulator, and the effector components are involved in attaining synchronous regulation of signaling. Optical modulation of the multicomponent network requires either receptor to effector encoded in a single ORF or direct modulation of the effector domain through bypassing all upstream players. Recently discovered modular rhodopsins like rhodopsin guanylate cyclase (RhoGC) and rhodopsin phosphodiesterase (RhoPDE) paves the way to establish a proof of concept for utilization of complex rhodopsin (modular rhodopsin) for optogenetic applications. Light sensor coupled modular system could be expressed in any cell type and hence holds great potential in the advancement of optogenetics 2.0 which would enable manipulating the entire relevant cell signaling system. Here, we had identified 50 novel modular rhodopsins with variant domains and their diverse cognate signaling cascades encoded in a single ORF, which are associated with specialized functions in the cells. These novel modular algal rhodopsins have been characterized based on their sequence and structural homology with previously reported rhodopsins. The presented novel modular rhodopsins with various effector domains leverage the potential to expand the optogenetic tool kit to regulate various cellular signaling pathways across the diverse biological model systems.
光门控离子通道和离子泵视紫红质被广泛用作光遗传学工具,它们能够控制电可兴奋细胞,原因如下:(1)它们是单组分系统,即其光感应和离子传导功能由7个跨膜结构域编码;(2)它们具有快速动力学,暗热恢复时间短。在细胞信号传导中,信号受体、调节剂和效应器组件参与实现信号的同步调节。对多组分网络的光学调制需要单个开放阅读框(ORF)中编码的受体到效应器,或者通过绕过所有上游元件直接调制效应器结构域。最近发现的模块化视紫红质,如视紫红质鸟苷酸环化酶(RhoGC)和视紫红质磷酸二酯酶(RhoPDE),为利用复杂视紫红质(模块化视紫红质)进行光遗传学应用建立概念验证铺平了道路。光传感器耦合模块化系统可以在任何细胞类型中表达,因此在光遗传学2.0的发展中具有巨大潜力,这将能够操纵整个相关的细胞信号系统。在这里,我们鉴定了50种具有变体结构域的新型模块化视紫红质,它们在单个开放阅读框中编码了不同的同源信号级联,这些信号级联与细胞中的特定功能相关。这些新型模块化藻类视紫红质已根据其与先前报道的视紫红质的序列和结构同源性进行了表征。所展示的具有各种效应器结构域的新型模块化视紫红质利用了扩展光遗传学工具包的潜力,以调节不同生物模型系统中的各种细胞信号通路。