α-Actinin-2 couples to cardiac Kv1.5 channels, regulating current density and channel localization in HEK cells

被引:78
作者
Maruoka, ND [1 ]
Steele, DF [1 ]
Au, BPY [1 ]
Dan, P [1 ]
Zhang, X [1 ]
Moore, EDW [1 ]
Fedida, D [1 ]
机构
[1] Univ British Columbia, Dept Physiol, Vancouver, BC V6T 1Z3, Canada
来源
FEBS LETTERS | 2000年 / 473卷 / 02期
基金
英国医学研究理事会;
关键词
alpha-actinin-2; K+ channel; Kv1.5; gating;
D O I
10.1016/S0014-5793(00)01521-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Voltage-gated K+ (Kv) channels are particularly important in the physiology of excitable cells in the heart and the brain. PSD-95 is known to cluster Shaker channels and NMDA receptors and the latter is known to couple through alpha-actinin-2 to the post-synaptic cytoskeleton [Wyszynski et al, (1997) Nature 385, 439-442], but the mechanisms by which Ky channels are linked to the actin cytoskeleton and clustered at specific sites in the heart are unknown. Here we provide evidence that Kv1.5 channels, widely expressed in the cardiovascular system, bind with alpha-actinin-2, Human Kv1.5 interacts via its N-terminus/core region and can be immunoprecipitated with alpha-actinin-2 both after in vitro translation and from HEK cells expressing both proteins, The ion channels and alpha-actinin-2 colocalize at the membrane in HEK cells, where disruption of the actin cytoskeleton and antisense constructs to alpha-actinin-2 modulate the ion and gating current density. (C) 2000 Federation of European Biochemical Societies.
引用
收藏
页码:188 / 194
页数:7
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