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首页> 外文期刊>Biochimica et biophysica acta. Molecular cell research >Capturing single L-type Ca2+ channel function with optics
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Capturing single L-type Ca2+ channel function with optics

机译:使用光学器件捕获单个L型Ca2 +通道功能

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摘要

Advances in imaging technology have allowed optical analysis of Ca2+-permeable ion channel activity. Here, we briefly review novel developments in optical recording of L-type voltage-dependent Ca2+ 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 Ca2+ 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.
机译:成像技术的进步已允许对Ca2 +渗透性离子通道活性进行光学分析。在这里,我们简要地回顾具有高时空分辨率的L型电压依赖性Ca2 +通道(LTCC)功能的光学记录的新进展。讨论了支持使用全内反射荧光(TIRF)显微镜对通道活性进行光学测量的基本原理,以及通过应用该方法揭示的LTCC的新功能特性。通过单个LTCC(“ LTCC小火花”)对Ca2 +流入的可视化表明,通道活动在区域上是异质的,并且群集通道能够以协作或“耦合”的方式运行。根据这些发现,我们描述了一种当前的分子模型,用于在生理和病理环境中对LTCC活性进行局部控制和耦合门控。本文是名为“第十二届欧洲钙研讨会”的特刊的一部分。

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