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使用光毒性荧光蛋白KillerRed的生色团辅助光灭活(CALI)。

Chromophore-assisted light inactivation (CALI) using the phototoxic fluorescent protein KillerRed.

作者信息

Bulina Maria E, Lukyanov Konstantin A, Britanova Olga V, Onichtchouk Daria, Lukyanov Sergey, Chudakov Dmitriy M

机构信息

Institute of Bioorganic Chemistry, Russian Academy of Sciences, Miklukho-Maklaya 16/10, Moscow 117997, Russia.

出版信息

Nat Protoc. 2006;1(2):947-53. doi: 10.1038/nprot.2006.89.

Abstract

The phototoxic red fluorescent GFP-like protein KillerRed has recently been described. The phototoxicity of KillerRed exceeds that of EGFP by at least 1,000-fold, making it the first fully genetically encoded photosensitizer. KillerRed opens up new possibilities for precise light-induced cell killing and target protein inactivation. Because KillerRed is encoded by a gene, it can be expressed in a spatially and temporally regulated manner, under a chosen promoter, and fused with the desired protein of interest or localization signal. Here we provide a protocol for target protein inactivation in cell culture using KillerRed. As KillerRed is a new tool, the protocol focuses on aspects that will allow users to maximize the potential of this protein, guiding the design of chimeric constructs, recommended control experiments and preferred illumination parameters. The protocol, which describes target protein visualization and subsequent inactivation, is a 2- or 3-d procedure.

摘要

最近发现了一种具有光毒性的红色荧光类绿色荧光蛋白(GFP)——杀伤红蛋白(KillerRed)。杀伤红蛋白的光毒性比增强型绿色荧光蛋白(EGFP)至少高1000倍,使其成为首个完全由基因编码的光敏剂。杀伤红蛋白为精确的光诱导细胞杀伤和靶蛋白失活开辟了新的可能性。由于杀伤红蛋白由基因编码,它可以在选定的启动子控制下,以空间和时间调控的方式表达,并与所需的目标蛋白或定位信号融合。在此,我们提供了一种利用杀伤红蛋白在细胞培养中使靶蛋白失活的方法。由于杀伤红蛋白是一种新工具,该方法着重于能让用户最大化发挥这种蛋白潜力的方面,指导嵌合构建体的设计、推荐的对照实验以及优选的光照参数。该方法描述了靶蛋白的可视化及随后的失活过程,是一个为期2天或3天的实验步骤。

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