Mechanosensitive ion channels and the peptide inhibitor GsMTx-4: History, properties, mechanisms and pharmacology

被引:139
|
作者
Bowman, Charles L. [1 ]
Gottlieb, Philip A.
Suchyna, Thomas M.
Murphy, Yolanda K.
Sachs, Frederick
机构
[1] SUNY Buffalo, Ctr Single Mol Biophys, Buffalo, NY 14214 USA
[2] SUNY Buffalo, Dept Physiol & Biophys, Buffalo, NY 14214 USA
关键词
D O I
10.1016/j.toxicon.2006.09.030
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Sensing the energy from mechanical inputs is ubiquitous-and perhaps the oldest form of biological energy transduction. However, the tools available to probe the mechanisms of transduction are far fewer than for the chemical and electric field sensitive transducers. The one pharmacological tool available for mechansensitive ion channels (MSCs) is a peptide (GsMTx-4) isolated from venom of the tarantula, Grammostola spatulata, that blocks cationic MSCs found in non-specialized eukaryotic tissues. In this review, we summarize the current knowledge of GsMTx-4, and discuss the inevitable crosstalk between the MSC behavior and the mechanical properties of the cell cortex. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:249 / 270
页数:22
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