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Analysis of conventional and unconventional trafficking of CFTR and other membrane proteins

Authors
 Heon Yung Gee  ;  Joo Young Kim  ;  Min Goo Lee 
Citation
 Methods in Molecular Biology (Clifton, N.J.), Vol.1270 : 137-154, 2015 
Journal Title
 Methods in Molecular Biology (Clifton, N.J.) 
Issue Date
2015
MeSH
Cell Line ; Cystic Fibrosis Transmembrane Conductance Regulator/metabolism* ; Endocytosis ; Fluorescent Antibody Technique ; Humans ; Immunohistochemistry ; Membrane Proteins/metabolism* ; Microscopy, Fluorescence ; Protein Transport ; Secretory Pathway
Keywords
Membrane protein ; Unconventional trafficking ; Cystic fibrosis transmembrane conductance regulator (CFTR) ; Surface biotinylation ; Immunofluorescence staining
Abstract
The cystic fibrosis transmembrane conductance regulator (CFTR) is a polytopic transmembrane protein that functions as a cAMP-activated anion channel at the apical membrane of epithelial cells. Mutations in CFTR cause cystic fibrosis and are also associated with monosymptomatic diseases in the lung, pancreas, intestines, and vas deferens. Many disease-causing CFTR mutations, including the deletion of a single phenylalanine residue at position 508 (ΔF508-CFTR), result in protein misfolding and trafficking defects. Therefore, intracellular trafficking of wild-type and mutant CFTR has been studied extensively, and results from these studies significantly contribute to our general understanding of mechanisms involved in the cell-surface trafficking of membrane proteins. CFTR is a glycoprotein that undergoes complex N-glycosylation as it passes through Golgi-mediated conventional exocytosis. Interestingly, results from recent studies revealed that CFTR and other membrane proteins can reach the plasma membrane via an unconventional alternative route that bypasses Golgi in specific cellular conditions. Here, we describe methods that have been used to investigate the conventional and unconventional surface trafficking of CFTR. With appropriate modifications, the protocols described in this chapter can also be applied to studies investigating the intracellular trafficking of other plasma membrane proteins.
Full Text
http://link.springer.com/protocol/10.1007%2F978-1-4939-2309-0_11
DOI
10.1007/978-1-4939-2309-0_11
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Pharmacology (약리학교실) > 1. Journal Papers
Yonsei Authors
Kim, Joo Young(김주영) ORCID logo https://orcid.org/0000-0003-2623-1491
Lee, Min Goo(이민구) ORCID logo https://orcid.org/0000-0001-7436-012X
Gee, Heon Yung(지헌영) ORCID logo https://orcid.org/0000-0002-8741-6177
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/155697
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