Costantini Lindsey, Snapp Erik
Department of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, New York.
Curr Protoc Cell Biol. 2013 Sep 24;60:21.7.1-21.7.29. doi: 10.1002/0471143030.cb2107s60.
This unit describes approaches and tools for studying the dynamics and organization of endoplasmic reticulum (ER) membranes and proteins in living cells using fluorescence microscopy. The ER plays a key role in secretory protein biogenesis, calcium regulation, and lipid synthesis. However, study of these processes has often been restricted to biochemical assays that average millions of lysed cells or imaging of static fixed cells. With new fluorescent protein (FP) reporter tools, sensitive commercial microscopes, and photobleaching techniques, investigators can interrogate the behaviors of ER proteins, membranes, and stress pathways in single live cells. Solutions are described for imaging challenges relevant to the ER, including the mobility of ER membranes, a range of ER structures, and the influence of post-translational modifications on FP reporters. Considerations for performing photobleaching assays for ER proteins are discussed. Finally, reporters and drugs for studying misfolded secretory protein stress and the unfolded protein response are described.
本单元介绍了利用荧光显微镜研究活细胞内质网(ER)膜和蛋白质的动力学及组织的方法和工具。内质网在分泌蛋白生物合成、钙调节和脂质合成中起关键作用。然而,这些过程的研究通常局限于对数百万裂解细胞进行平均的生化分析或对静态固定细胞的成像。借助新型荧光蛋白(FP)报告工具、灵敏的商用显微镜和光漂白技术,研究人员可以在单个活细胞中探究内质网蛋白、膜和应激途径的行为。文中描述了针对与内质网相关的成像挑战的解决方案,包括内质网膜的流动性、一系列内质网结构以及翻译后修饰对FP报告分子的影响。讨论了对内质网蛋白进行光漂白分析的注意事项。最后,介绍了用于研究错误折叠的分泌蛋白应激和未折叠蛋白反应的报告分子和药物。