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使用重组靶向发光探针测量钙离子浓度。

Measurements of Ca²⁺ concentration with recombinant targeted luminescent probes.

作者信息

Ottolini Denis, Calì Tito, Brini Marisa

机构信息

Department of Biomedical Sciences, University of Padova, Padova, Italy.

出版信息

Methods Mol Biol. 2013;937:273-91. doi: 10.1007/978-1-62703-086-1_17.

Abstract

In the last two decades the study of Ca(2+) homeostasis in living cells has been enhanced by the explosive development of genetically encoded Ca(2+)-indicators. The cloning of the Ca(2+)-sensitive photoprotein aequorin and of the green fluorescent protein (GFP) from the jellyfish Aequorea victoria has been enormously advantageous. As polypeptides, aequorin and GFP allow their endogenous production in cell systems as diverse as bacteria, yeast, slime molds, plants, and mammalian cells. Moreover, it is possible to specifically localize them within the cell by including defined targeting signals in the amino acid sequence. These two proteins have been extensively engineered to obtain several recombinant probes for different biological parameters, among which Ca(2+) concentration reporters are probably the most relevant. The GFP-based Ca(2+) probes and aequorin are widely employed in the study of intracellular Ca(2+) homeostasis. The new generation of bioluminescent probes that couple the Ca(2+) sensitivity of aequorin to GFP fluorescence emission allows real-time measurements of subcellular Ca(2+) changes in single cell imaging experiments and the video-imaging of Ca(2+) concentrations changes in live transgenic animals that express GFP-aequorin bifunctional probes.

摘要

在过去二十年中,基因编码钙指示剂的迅猛发展推动了对活细胞中钙离子稳态的研究。来自维多利亚多管水母的钙敏感光蛋白水母发光蛋白和绿色荧光蛋白(GFP)的克隆带来了极大便利。作为多肽,水母发光蛋白和绿色荧光蛋白能够在诸如细菌、酵母、黏菌、植物和哺乳动物细胞等多种细胞系统中内源性产生。此外,通过在氨基酸序列中包含特定的靶向信号,可以将它们特异性地定位在细胞内。这两种蛋白质经过广泛改造,以获得用于不同生物学参数的多种重组探针,其中钙离子浓度报告基因可能最为重要。基于绿色荧光蛋白的钙离子探针和水母发光蛋白被广泛应用于细胞内钙离子稳态的研究。新一代生物发光探针将水母发光蛋白的钙离子敏感性与绿色荧光蛋白的荧光发射相结合,能够在单细胞成像实验中实时测量亚细胞钙离子变化,并对表达绿色荧光蛋白 - 水母发光蛋白双功能探针的活体转基因动物中的钙离子浓度变化进行视频成像。

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