Nystoriak Matthew A, Nieves-Cintrón Madeline, Navedo Manuel F
Department of Pharmacology, University of California Davis, Davis, CA, USA.
Biochim Biophys Acta. 2013 Jul;1833(7):1657-64. doi: 10.1016/j.bbamcr.2012.10.027. Epub 2012 Nov 1.
Advances in imaging technology have allowed optical analysis of Ca(2+)-permeable ion channel activity. Here, we briefly review novel developments in optical recording of L-type voltage-dependent Ca(2+) channel (LTCC) function with high spatial and temporal resolution. Underlying principles supporting the use of total internal reflection fluorescence (TIRF) microscopy for optical measurement of channel activity and new functional characteristics of LTCCs revealed by application of this approach are discussed. Visualization of Ca(2+) influx through single LTCCs ("LTCC sparklets") has demonstrated that channel activity is regionally heterogeneous and that clustered channels are capable of operating in a cooperative, or "coupled" manner. In light of these findings, we describe a current molecular model for the local control of LTCC activity and coupled gating in physiological and pathological contexts. This article is part of a Special Issue entitled: 12th European Symposium on Calcium.
成像技术的进步使得对钙离子通透离子通道活性进行光学分析成为可能。在此,我们简要回顾利用高空间和时间分辨率对L型电压依赖性钙通道(LTCC)功能进行光学记录的新进展。文中讨论了支持使用全内反射荧光(TIRF)显微镜进行通道活性光学测量的基本原理,以及应用该方法所揭示的LTCC的新功能特性。通过单个LTCC(“LTCC小火花”)对钙离子内流的可视化已证明通道活性存在区域异质性,并且成簇的通道能够以协同或“耦合”方式运作。鉴于这些发现,我们描述了一种当前的分子模型,用于在生理和病理情况下对LTCC活性和耦合门控进行局部控制。本文是名为“第12届欧洲钙研讨会”的特刊的一部分。