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{"title":"Probing Endoplasmic Reticulum Dynamics using Fluorescence Imaging and Photobleaching Techniques","authors":"Lindsey Costantini, Erik Snapp","doi":"10.1002/0471143030.cb2107s60","DOIUrl":null,"url":null,"abstract":"<p>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. <i>Curr. Protoc. Cell Biol</i>. 60:21.7.1-21.7.29. © 2013 by John Wiley & Sons, Inc.</p>","PeriodicalId":40051,"journal":{"name":"Current Protocols in Cell Biology","volume":"60 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2018-02-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/0471143030.cb2107s60","citationCount":"18","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Cell Biology","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/0471143030.cb2107s60","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 18
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Abstract
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. Curr. Protoc. Cell Biol . 60:21.7.1-21.7.29. © 2013 by John Wiley & Sons, Inc.
利用荧光成像和光漂白技术探测内质网动力学
本单元描述了使用荧光显微镜研究活细胞内质网(ER)膜和蛋白质的动力学和组织的方法和工具。内质网在分泌蛋白生物生成、钙调节和脂质合成中起关键作用。然而,对这些过程的研究通常局限于平均数百万裂解细胞的生化分析或静态固定细胞的成像。有了新的荧光蛋白(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询问内质网蛋白、膜和应激途径的行为。描述了与内质网相关的成像挑战的解决方案,包括内质网膜的移动性,内质网结构的范围,以及翻译后修饰对FP报告的影响。讨论了内质网蛋白进行光漂白试验的考虑因素。最后,介绍了用于研究错误折叠分泌蛋白应激和未折叠蛋白反应的载体和药物。咕咕叫。Protoc。细胞生物学。60:21.7.1-21.7.29。©2013 by John Wiley &儿子,Inc。
本文章由计算机程序翻译,如有差异,请以英文原文为准。