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Live-Cell Imaging of Physiologically Relevant Metal Ions Using Genetically Encoded FRET-Based Probes

机译:使用基于遗传编码的基于FRET的探针的生理相关金属离子的活细胞成像

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Essential biochemical reactions and processes within living organisms are coupled to subcellular fluctuations of metal ions. Disturbances in cellular metal ion homeostasis are frequently associated with pathological alterations, including neurotoxicity causing neurodegeneration, as well as metabolic disorders or cancer. Considering these important aspects of the cellular metal ion homeostasis in health and disease, measurements of subcellular ion signals are of broad scientific interest. The investigation of the cellular ion homeostasis using classical biochemical methods is quite difficult, often even not feasible or requires large cell numbers. Here, we report of genetically encoded fluorescent probes that enable the visualization of metal ion dynamics within individual living cells and their organelles with high temporal and spatial resolution. Generally, these probes consist of specific ion binding domains fused to fluorescent protein(s), altering their fluorescent properties upon ion binding. This review focuses on the functionality and potential of these genetically encoded fluorescent tools which enable monitoring (sub)cellular concentrations of alkali metals such as K + , alkaline earth metals including Mg 2+ and Ca 2+ , and transition metals including Cu + /Cu 2+ and Zn 2+ . Moreover, we discuss possible approaches for the development and application of novel metal ion biosensors for Fe 2+ /Fe 3+ , Mn 2+ and Na + .
机译:生物体内的必需生化反应和过程偶联到金属离子的亚细胞波动。细胞金属离子稳态中的扰动通常与病理改变相关,包括导致神经变性的神经毒性,以及代谢障碍或癌症。考虑到健康和疾病中细胞金属离子稳态的这些重要方面,亚细胞离子信号的测量具有广泛的科学兴趣。使用经典生化方法对细胞离子稳态的研究非常困难,甚至不可行或需要大的细胞数。在这里,我们报告了遗传编码的荧光探针,使单个活细胞和它们的细胞器内的金属离子动力学的可视化具有高的时间和空间分辨率。通常,这些探针由与荧光蛋白稠合的特定离子结合结构域组成,在离子结合时改变它们的荧光性质。本综述重点介绍了这些遗传编码的荧光工具的功能和潜力,其能够在包括Mg 2+和Ca 2+的K +,碱土金属如K +,包括Cu + / Cu的过渡金属(包括Cu + / Cu)的碱金属的监测(子)细胞浓度2+和Zn 2+。此外,我们讨论了Fe 2+ / Fe 3+,Mn 2+和Na +的新型金属离子体传感器的开发和应用的可能方法。

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