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红光发射的荧光蛋白和光激活蛋白的工程学进展。

Advances in engineering of fluorescent proteins and photoactivatable proteins with red emission.

机构信息

Department of Anatomy and Structural Biology and Gruss-Lipper Biophotonics Center, Albert Einstein College of Medicine, Bronx, NY 10461, USA.

出版信息

Curr Opin Chem Biol. 2010 Feb;14(1):23-9. doi: 10.1016/j.cbpa.2009.10.011. Epub 2009 Nov 14.

Abstract

Monomeric fluorescent proteins of different colors are widely used to study behavior and targeting of proteins in living cells. Fluorescent proteins that irreversibly change their spectral properties in response to light irradiation of a specific wavelength, or photoactivate, have become increasingly popular to image intracellular dynamics and superresolution protein localization. Until recently, however, no optimized monomeric red fluorescent proteins and red photoactivatable proteins have been available. Furthermore, monomeric fluorescent proteins, which change emission from blue to red simply with time, so-called fluorescent timers, were developed to study protein age and turnover. Understanding of chemical mechanisms of the chromophore maturation or photoactivation into a red form will further advance engineering of fluorescent timers and photoactivatable proteins with enhanced and novel properties.

摘要

不同颜色的单体荧光蛋白被广泛用于研究活细胞中蛋白质的行为和靶向。不可逆地改变其光谱特性以响应特定波长的光照射或光激活的荧光蛋白已越来越受欢迎,用于成像细胞内动力学和超分辨率蛋白质定位。然而,直到最近,还没有优化的单体红色荧光蛋白和红色光激活蛋白可用。此外,单体荧光蛋白,即所谓的荧光定时器,随着时间的推移简单地从蓝色变为红色,被开发用于研究蛋白质的年龄和周转率。对生色团成熟或光激活成红色形式的化学机制的理解将进一步推进具有增强和新颖特性的荧光定时器和光激活蛋白的工程。

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