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翻转光开关:光控离子通道

Flipping the Photoswitch: Ion Channels Under Light Control.

作者信息

McKenzie Catherine K, Sanchez-Romero Inmaculada, Janovjak Harald

机构信息

Institute of Science and Technology Austria, Am Campus 1, A-3400, Klosterneuburg, Austria.

出版信息

Adv Exp Med Biol. 2015;869:101-17. doi: 10.1007/978-1-4939-2845-3_6.

Abstract

Nature has incorporated small photochromic molecules, colloquially termed 'photoswitches', in photoreceptor proteins to sense optical cues in phototaxis and vision. While Nature's ability to employ light-responsive functionalities has long been recognized, it was not until recently that scientists designed, synthesized and applied synthetic photochromes to manipulate many of which open rapidly and locally in their native cell types, biological processes with the temporal and spatial resolution of light. Ion channels in particular have come to the forefront of proteins that can be put under the designer control of synthetic photochromes. Photochromic ion channel controllers are comprised of three classes, photochromic soluble ligands (PCLs), photochromic tethered ligands (PTLs) and photochromic crosslinkers (PXs), and in each class ion channel functionality is controlled through reversible changes in photochrome structure. By acting as light-dependent ion channel agonists, antagonist or modulators, photochromic controllers effectively converted a wide range of ion channels, including voltage-gated ion channels, 'leak channels', tri-, tetra- and pentameric ligand-gated ion channels, and temperature-sensitive ion channels, into man-made photoreceptors. Control by photochromes can be reversible, unlike in the case of 'caged' compounds, and non-invasive with high spatial precision, unlike pharmacology and electrical manipulation. Here, we introduce design principles of emerging photochromic molecules that act on ion channels and discuss the impact that these molecules are beginning to have on ion channel biophysics and neuronal physiology.

摘要

自然界已将一些小的光致变色分子(通俗地称为“光开关”)纳入光感受器蛋白中,以感知趋光性和视觉中的光学信号。虽然自然界利用光响应功能的能力早已得到认可,但直到最近科学家们才设计、合成并应用合成光致变色剂来操纵许多生物过程,其中许多光致变色剂在其天然细胞类型中能迅速且局部地打开,具有光的时间和空间分辨率。特别是离子通道已成为可以在合成光致变色剂的设计控制下的蛋白质的前沿领域。光致变色离子通道控制器分为三类:光致变色可溶性配体(PCL)、光致变色 tethered 配体(PTL)和光致变色交联剂(PX),在每一类中,离子通道功能都是通过光致变色剂结构的可逆变化来控制的。通过充当光依赖性离子通道激动剂、拮抗剂或调节剂,光致变色控制器有效地将包括电压门控离子通道、“泄漏通道”、三聚体、四聚体和五聚体配体门控离子通道以及温度敏感离子通道在内的多种离子通道转化为人造光感受器。与“笼形”化合物不同,光致变色剂的控制可以是可逆的,并且与药理学和电操纵不同,具有高空间精度的非侵入性。在这里,我们介绍作用于离子通道的新兴光致变色分子的设计原理,并讨论这些分子开始对离子通道生物物理学和神经元生理学产生的影响。

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