Department of Physiology, University of California, San Francisco, San Francisco, CA 94143-2140, USA.
Cell. 2010 May 28;141(5):834-45. doi: 10.1016/j.cell.2010.03.052.
Toxins have evolved to target regions of membrane ion channels that underlie ligand binding, gating, or ion permeation, and have thus served as invaluable tools for probing channel structure and function. Here, we describe a peptide toxin from the Earth Tiger tarantula that selectively and irreversibly activates the capsaicin- and heat-sensitive channel, TRPV1. This high-avidity interaction derives from a unique tandem repeat structure of the toxin that endows it with an antibody-like bivalency. The "double-knot" toxin traps TRPV1 in the open state by interacting with residues in the presumptive pore-forming region of the channel, highlighting the importance of conformational changes in the outer pore region of TRP channels during activation.
毒素已经进化到能够靶向位于配体结合、门控或离子渗透的膜离子通道的区域,因此它们已成为探测通道结构和功能的宝贵工具。在这里,我们描述了一种来自地球虎蛛的肽毒素,它选择性地和不可逆地激活辣椒素和热敏通道 TRPV1。这种高亲和力的相互作用源自毒素的独特串联重复结构,赋予它类似抗体的二价性。“双结”毒素通过与通道假定的孔形成区域中的残基相互作用,将 TRPV1 困在开放状态,这突出了 TRP 通道外孔区域在激活过程中构象变化的重要性。