Mediterranean Institute of Neurobiology, INSERM U901 Marseille, France.
Front Mol Neurosci. 2009 Dec 4;2:15. doi: 10.3389/neuro.02.015.2009. eCollection 2009.
This review briefly discusses the main approaches for monitoring chloride (Cl(-)), the most abundant physiological anion. Noninvasive monitoring of intracellular Cl(-) ([Cl(-)]i) is a challenging task owing to two main difficulties: (i) the low transmembrane ratio for Cl(-), approximately 10:1; and (ii) the small driving force for Cl(-), as the Cl(-) reversal potential (E(Cl)) is usually close to the resting potential of the cells. Thus, for reliable monitoring of intracellular Cl(-), one has to use highly sensitive probes. From several methods for intracellular Cl(-) analysis, genetically encoded chloride indicators represent the most promising tools. Recent achievements in the development of genetically encoded chloride probes are based on the fact that yellow fluorescent protein (YFP) exhibits Cl(-)-sensitivity. YFP-based probes have been successfully used for quantitative analysis of Cl(-) transport in different cells and for high-throughput screening of modulators of Cl(-)-selective channels. Development of a ratiometric genetically encoded probe, Clomeleon, has provided a tool for noninvasive estimation of intracellular Cl(-) concentrations. While the sensitivity of this protein to Cl(-) is low (EC(50) about 160 mM), it has been successfully used for monitoring intracellular Cl(-) in different cell types. Recently a CFP-YFP-based probe with a relatively high sensitivity to Cl(-) (EC(50) about 30 mM) has been developed. This construct, termed Cl-Sensor, allows ratiometric monitoring using the fluorescence excitation ratio. Of particular interest are genetically encoded probes for monitoring of ion channel distribution and activity. A new molecular probe has been constructed by introducing into the cytoplasmic domain of the Cl(-)-selective glycine receptor (GlyR) channel the CFP-YFP-based Cl-Sensor. This construct, termed BioSensor-GlyR, has been successfully expressed in cell lines. The new genetically encoded chloride probes offer means of screening pharmacological agents, analysis of Cl(-) homeostasis and functions of Cl(-)-selective channels under different physiological and pathological conditions.
本文简要讨论了监测氯离子(Cl(-))的主要方法,Cl(-)是最丰富的生理阴离子。由于两个主要困难,非侵入性监测细胞内 Cl(-) ([Cl(-)])是一项具有挑战性的任务:(i)Cl(-)的跨膜比值低,约为 10:1;(ii)Cl(-)的驱动力小,因为 Cl(-)反转电位(E(Cl))通常接近细胞的静息电位。因此,为了可靠地监测细胞内 Cl(-),必须使用高灵敏度的探针。在几种细胞内 Cl(-)分析方法中,遗传编码的氯离子指示剂代表最有前途的工具。遗传编码的氯离子探针的最新进展基于以下事实:黄色荧光蛋白(YFP)表现出 Cl(-)敏感性。基于 YFP 的探针已成功用于不同细胞中 Cl(-)转运的定量分析,以及 Cl(-)选择性通道调节剂的高通量筛选。比率型遗传编码探针 Clomeleon 的开发为非侵入性估计细胞内 Cl(-)浓度提供了一种工具。虽然该蛋白对 Cl(-)的灵敏度较低(EC(50)约 160 mM),但它已成功用于监测不同细胞类型中的细胞内 Cl(-)。最近,开发了一种对 Cl(-)具有相对高灵敏度(EC(50)约 30 mM)的基于 CFP-YFP 的探针,该探针称为 Cl-Sensor,允许使用荧光激发比进行比率监测。特别感兴趣的是用于监测离子通道分布和活性的遗传编码探针。通过将基于 CFP-YFP 的 Cl-Sensor 引入 Cl(-)选择性甘氨酸受体(GlyR)通道的细胞质结构域,构建了一种新型分子探针。该构建体,称为 BioSensor-GlyR,已成功在细胞系中表达。新型遗传编码氯离子探针为筛选药理学试剂、分析 Cl(-)稳态和不同生理和病理条件下 Cl(-)选择性通道的功能提供了手段。