| Literature DB >> 28862339 |
Krishna C Mudumbi1, Weidong Yang1.
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.Entities:
Keywords: Cellular imaging; FRAP; membrane biophysics; super-resolution; transmembrane protein
Mesh:
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Year: 2017 PMID: 28862339 PMCID: PMC5879780 DOI: 10.1002/cpcb.27
Source DB: PubMed Journal: Curr Protoc Cell Biol ISSN: 1934-2616