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基因编码荧光工具:照亮内质网到高尔基体运输。

Genetically encoded fluorescent tools: Shining a little light on ER-to-Golgi transport.

机构信息

Division of Biological Sciences, Center for Structural & Functional Neuroscience, University of Montana, Missoula, MT, 59812, USA.

Division of Biological Sciences, Center for Structural & Functional Neuroscience, University of Montana, Missoula, MT, 59812, USA.

出版信息

Free Radic Biol Med. 2022 Apr;183:14-24. doi: 10.1016/j.freeradbiomed.2022.03.004. Epub 2022 Mar 8.

Abstract

Since the first fluorescent proteins (FPs) were identified and isolated over fifty years ago, FPs have become commonplace yet indispensable tools for studying the constitutive secretory pathway in live cells. At the same time, genetically encoded chemical tags have provided a new use for much older fluorescent dyes. Innovation has also produced several specialized methods to allow synchronous release of cargo proteins from the endoplasmic reticulum (ER), enabling precise characterization of sequential trafficking steps in the secretory pathway. Without the constant innovation of the researchers who design these tools to control, image, and quantitate protein secretion, major discoveries about ER-to-Golgi transport and later stages of the constitutive secretory pathway would not have been possible. We review many of the tools and tricks, some 25 years old and others brand new, that have been successfully implemented to study ER-to-Golgi transport in intact and living cells.

摘要

自 50 多年前首次鉴定和分离出荧光蛋白 (FPs) 以来,FPs 已成为研究活细胞中组成性分泌途径的常用且不可或缺的工具。与此同时,基因编码的化学标签为更古老的荧光染料提供了新的用途。创新还产生了几种专门的方法,可允许货物蛋白从内质网 (ER) 同步释放,从而能够精确表征分泌途径中的连续运输步骤。如果没有设计这些工具来控制、成像和定量蛋白质分泌的研究人员的不断创新,关于 ER 到高尔基体运输以及组成性分泌途径的后期阶段的重大发现将是不可能的。我们回顾了许多工具和技巧,其中一些已有 25 年的历史,而另一些则是全新的,这些工具和技巧已成功地用于研究完整和活细胞中的 ER 到高尔基体运输。

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ER-to-Golgi Transport: A Sizeable Problem.内质网到高尔基体的运输:一个相当大的问题。
Trends Cell Biol. 2019 Dec;29(12):940-953. doi: 10.1016/j.tcb.2019.08.007. Epub 2019 Oct 17.

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