Chen Yuting, Lu Linjie, Ye Shixin
Shanghai Key Laboratory of Regulatory Biology, Institute of Biomedical Sciences and School of Life Sciences, East China Normal University (ECNU), Shanghai, China.
Université Pierre-et-Marie-Curie, Laboratory of Computational and Quantitative Biology (LCQB), Institute of Biology Paris-Seine, Paris, France.
Yale J Biol Med. 2017 Dec 19;90(4):599-610. eCollection 2017 Dec.
Nature has invented photoreceptor proteins that are involved in sensing and response to light in living organisms. Genetic code expansion (GCE) technology has provided new tools to transform light insensitive proteins into novel photoreceptor proteins. It is achieved by the site-specific incorporation of unnatural amino acids (Uaas) that carry light sensitive moieties serving as "pigments" that react to light via photo-decaging, cross-linking, or isomerization. Over the last two decades, various proteins including ion channels, GPCRs, transporters, and kinases have been successfully rendered light responsive owing to the functionalities of Uaas. Very recently, Cas9 protein has been engineered to enable light activation of genomic editing by CRISPR. Those novel proteins have not only led to discoveries of dynamic protein conformational changes with implications in diseases, but also facilitated the screening of ligand-protein and protein-protein interactions of pharmacological significance. This review covers the genetic editing principles for genetic code expansion and design concepts that guide the engineering of light-sensitive proteins. The applications have brought up a new concept of "optoproteomics" that, in contrast to "optogenetics," aims to combine optical methods and site-specific proteomics for investigating and intervening in biological functions.
自然界已经发明了光感受器蛋白,这些蛋白参与生物体对光的感知和响应。遗传密码扩展(GCE)技术提供了新工具,可将对光不敏感的蛋白转化为新型光感受器蛋白。这是通过位点特异性掺入携带光敏部分的非天然氨基酸(Uaa)来实现的,这些光敏部分充当“色素”,通过光脱笼、交联或异构化对光作出反应。在过去二十年中,由于Uaa的功能,包括离子通道、GPCR、转运蛋白和激酶在内的各种蛋白已成功实现光响应。最近,Cas9蛋白经过工程改造,能够通过CRISPR实现基因组编辑的光激活。这些新型蛋白不仅带来了对与疾病相关的动态蛋白构象变化的发现,还促进了具有药理学意义的配体-蛋白和蛋白-蛋白相互作用的筛选。本综述涵盖了遗传密码扩展的基因编辑原理以及指导光敏蛋白工程的设计概念。这些应用提出了一个“光蛋白质组学”的新概念,与“光遗传学”不同,它旨在将光学方法和位点特异性蛋白质组学结合起来,用于研究和干预生物学功能。