Connexin and gap junction degradation

被引:37
作者
Berthoud, VM
Tadros, PN
Beyer, EC
机构
[1] Univ Chicago, Dept Pediat, Chicago, IL 60637 USA
[2] Washington Univ, Sch Med, Div Cardiovasc, St Louis, MO 63110 USA
来源
METHODS-A COMPANION TO METHODS IN ENZYMOLOGY | 2000年 / 20卷 / 02期
关键词
D O I
10.1006/meth.1999.0935
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Many of the subunit proteins (connexins) that form gap junctions are rather dynamic, with half-lives of only a few hours. Thus, alterations in connexin turnover and degradation may represent significant mechanisms for the regulation of intercellular communication. We describe a pharmacological approach to determining pathways of connexin degradation. Cell cultures are left untreated or treated with inhibitors of lysosomal or proteasomal proteolysis. Changes in connexin levels, localization, or decay curves (derived from pulse-chase experiments) are assessed by immunoblotting, immunofluorescence, and immunoprecipitation, respectively. Such experiments have provided evidence that connexin43 degradation involves both the lysosome and the proteasome, (C) 2000 Academic Press.
引用
收藏
页码:180 / 187
页数:8
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