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{"title":"Determination of Membrane Protein Distribution on the Nuclear Envelope by Single-Point Single-Molecule FRAP.","authors":"Krishna C Mudumbi, Weidong Yang","doi":"10.1002/cpcb.27","DOIUrl":null,"url":null,"abstract":"<p><p>Nuclear envelope transmembrane proteins (NETs) are synthesized on the endoplasmic reticulum and then transported from the outer nuclear membrane (ONM) to the inner nuclear membrane (INM) in eukaryotic cells. The abnormal distribution of NETs has been associated with many human diseases. However, quantitative determination of the spatial distribution and translocation dynamics of NETs on the ONM and INM is still very limited in currently existing approaches. Here we demonstrate a single-point single-molecule fluorescence recovery after photobleaching (FRAP) microscopy technique that enables quick determination of distribution and translocation rates for NETs in vivo. © 2017 by John Wiley & Sons, Inc.</p>","PeriodicalId":40051,"journal":{"name":"Current Protocols in Cell Biology","volume":"76 ","pages":"21.11.1-21.11.13"},"PeriodicalIF":0.0000,"publicationDate":"2017-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpcb.27","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Cell Biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/cpcb.27","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}
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Abstract
Nuclear envelope transmembrane proteins (NETs) are synthesized on the endoplasmic reticulum and then transported from the outer nuclear membrane (ONM) to the inner nuclear membrane (INM) in eukaryotic cells. The abnormal distribution of NETs has been associated with many human diseases. However, quantitative determination of the spatial distribution and translocation dynamics of NETs on the ONM and INM is still very limited in currently existing approaches. Here we demonstrate a single-point single-molecule fluorescence recovery after photobleaching (FRAP) microscopy technique that enables quick determination of distribution and translocation rates for NETs in vivo. © 2017 by John Wiley & Sons, Inc.
单点单分子FRAP法测定核膜上膜蛋白分布。
真核细胞的核包膜跨膜蛋白(NETs)是在内质网上合成,然后由外核膜(ONM)转运到内核膜(INM)。NETs的异常分布与许多人类疾病有关。然而,在现有的方法中,对网络在ONM和INM上的空间分布和迁移动态的定量确定仍然非常有限。在这里,我们展示了光漂白后单点单分子荧光恢复(FRAP)显微镜技术,可以快速确定体内NETs的分布和易位率。©2017 by John Wiley & Sons, Inc。
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