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用于光遗传学应用的近红外光响应合成环二鸟苷单磷酸模块。

Near-infrared light responsive synthetic c-di-GMP module for optogenetic applications.

作者信息

Ryu Min-Hyung, Gomelsky Mark

机构信息

Department of Molecular Biology, University of Wyoming , 1000 East University Avenue, Dept. 3944, Laramie, Wyoming 82071, United States.

出版信息

ACS Synth Biol. 2014 Nov 21;3(11):802-10. doi: 10.1021/sb400182x. Epub 2014 Jan 28.

Abstract

Enormous potential of cell-based therapeutics is hindered by the lack of effective means to control genetically engineered cells in mammalian tissues. Here, we describe a synthetic module for remote photocontrol of engineered cells that can be adapted for such applications. The module involves photoactivated synthesis of cyclic dimeric GMP (c-di-GMP), a stable small molecule that is not produced by higher eukaryotes and therefore is suitable for orthogonal regulation. The key component of the photocontrol module is an engineered bacteriophytochrome diguanylate cyclase, which synthesizes c-di-GMP from GTP in a light-dependent manner. Bacteriophytochromes are particularly attractive photoreceptors because they respond to light in the near-infrared window of the spectrum, where absorption by mammalian tissues is minimal, and also because their chromophore, biliverdin IXα, is naturally available in mammalian cells. The second component of the photocontrol module, a c-di-GMP phosphodiesterase, maintains near-zero background levels of c-di-GMP in the absence of light, which enhances the photodynamic range of c-di-GMP concentrations. In the E. coli model used in this study, the intracellular c-di-GMP levels could be upregulated by light by >50-fold. Various c-di-GMP-responsive proteins and riboswitches identified in bacteria can be linked downstream of the c-di-GMP-mediated photocontrol module for orthogonal regulation of biological activities in mammals as well as in other organisms lacking c-di-GMP signaling. Here, we linked the photocontrol module to a gene expression output via a c-di-GMP-responsive transcription factor and achieved a 40-fold photoactivation of gene expression.

摘要

基于细胞的疗法的巨大潜力因缺乏在哺乳动物组织中控制基因工程细胞的有效手段而受到阻碍。在此,我们描述了一种用于工程细胞远程光控的合成模块,该模块可适用于此类应用。该模块涉及环二聚体鸟苷酸(c-di-GMP)的光活化合成,c-di-GMP是一种稳定的小分子,高等真核生物不会产生,因此适用于正交调节。光控模块的关键组件是一种工程化的细菌光敏色素二鸟苷酸环化酶,它以光依赖的方式从GTP合成c-di-GMP。细菌光敏色素是特别有吸引力的光感受器,因为它们对光谱中近红外窗口的光有反应,在该窗口中哺乳动物组织的吸收最小,还因为它们的发色团胆绿素IXα在哺乳动物细胞中天然存在。光控模块的第二个组件,一种c-di-GMP磷酸二酯酶,在无光条件下维持c-di-GMP的背景水平接近零,这增强了c-di-GMP浓度的光动力学范围。在本研究使用的大肠杆菌模型中,细胞内c-di-GMP水平可通过光照上调50倍以上。在细菌中鉴定出的各种c-di-GMP响应蛋白和核糖开关可连接到c-di-GMP介导的光控模块下游,用于对哺乳动物以及其他缺乏c-di-GMP信号的生物体中的生物活性进行正交调节。在此处,我们通过一个c-di-GMP响应转录因子将光控模块与基因表达输出相连接,并实现了基因表达40倍的光激活。

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