Elementary events underlying voltage-dependent G-protein inhibition of N-type calcium channels

被引:105
|
作者
Patil, PG
deLeon, M
Reed, RR
Dubel, S
Snutch, TP
Yue, DT
机构
[1] JOHNS HOPKINS UNIV, SCH MED, DEPT BIOMED ENGN, PROGRAM MOL & CELLULAR SYST PHYSIOL, BALTIMORE, MD 21205 USA
[2] JOHNS HOPKINS UNIV, SCH MED, DEPT NEUROSCI & MOLEC BIOL, BALTIMORE, MD 21205 USA
[3] JOHNS HOPKINS UNIV, SCH MED, DEPT GENET, BALTIMORE, MD 21205 USA
[4] JOHNS HOPKINS UNIV, SCH MED, HOWARD HUGHES MED INST, BALTIMORE, MD 21205 USA
[5] UNIV BRITISH COLUMBIA, BIOTECHNOL LAB, VANCOUVER, BC V6T 1Z3, CANADA
基金
美国国家卫生研究院; 英国医学研究理事会; 美国国家科学基金会;
关键词
D O I
10.1016/S0006-3495(96)79444-4
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Voltage-dependent G-protein inhibition of N-type calcium channels reduces presynaptic calcium entry, sharply attenuating neurotransmitter release, Studies in neurons demonstrate that G-proteins have multiple modulatory effects on N-type channels, The observed changes may reflect genuine complexity in G-protein action and/or the intricate interactions of multiple channels and receptors in neurons. Expression of recombinant M2-muscarinic receptors and N-type channels in HEK 293 cells allowed voltage-dependent inhibition to be studied in isolation. In this system, receptor-activated G-proteins had only one effect: a 10-fold increase in the time required for channels to first open following membrane depolarization. There were no changes in gating after the channel first opened, and unitary currents were not detectably altered by modulation. Despite its simplicity, this single change successfully accounts for the complex alterations in whole-cell current observed during G-protein inhibition in neurons.
引用
收藏
页码:2509 / 2521
页数:13
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