Structural insights into the regulatory mechanism Of IP3 receptor

被引:98
作者
Bosanac, I
Michikawa, T
Mikoshiba, K
Ikura, M
机构
[1] Univ Toronto, Ontario Canc Inst, Div Mol & Struct Biol, Toronto, ON M5G 2M9, Canada
[2] Univ Toronto, Dept Med Biophys, Toronto, ON M5G 2M9, Canada
[3] Univ Tokyo, Inst Med Sci, Div Mol Neurobiol, Dept Basic Med Sci, Tokyo 1088639, Japan
[4] Japan Sci & Technol Corp, Calcium Oscillat Project, Int Cooperat Res Project, Tokyo 1080071, Japan
[5] RIKEN, Brain Sci Inst, Dev Neurobiol Lab, Wako, Saitama 3510198, Japan
[6] Univ Tokyo, Inst Med Sci, Dept Basic Med Sci, Div Neural Signal Informat,NIT,IMSUT, Tokyo 1088639, Japan
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH | 2004年 / 1742卷 / 1-3期
关键词
calcium signaling; IP3; IP3 receptor structure;
D O I
10.1016/j.bbamcr.2004.09.016
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Inositol 1,4,5-trisphosphate receptors (IP3R) are intracellular Ca2+ release channels whose opening requires binding of two intracellular messengers IP3 and Ca2+. The regulation of IP3R function has also been shown to involve a variety of cellular proteins. Recent biochemical and structural analyses have deepened our understanding of how the IP3-operated Ca2+ channel functions. Specifically, the atomic resolution structure of the IP3-binding region has provided a sound structural basis for the receptor interaction with the natural ligand. Electron microscopic studies have also shed light on the overall shape of the tetrameric receptor. This review aims to provide comprehensive overview of the current information available on the structure and function relationship of IP3R. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:89 / 102
页数:14
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