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用于定量生物样品中钾离子浓度的基因编码钾离子指示剂的纯化与应用

Purification and Application of Genetically Encoded Potassium Ion Indicators for Quantification of Potassium Ion Concentrations within Biological Samples.

作者信息

Bischof H, Burgstaller S, Vujic N, Madl T, Kratky D, Graier W F, Malli R

机构信息

Gottfried Schatz Research Center, Molecular Biology and Biochemistry, Medical University of Graz, Graz, Austria.

BioTechMed-Graz, Graz, Austria.

出版信息

Curr Protoc Chem Biol. 2019 Sep;11(3):e71. doi: 10.1002/cpch.71.

Abstract

Vital cells maintain a steep potassium ion (K ) gradient across the plasma membrane. Intracellular potassium ion concentrations ([K ]) and especially the [K ] within the extracellular matrix are strictly regulated, the latter within a narrow range of ∼3.5 to 5.0 mM. Alterations of the extracellular K homeostasis are associated with severe pathological alterations and systemic diseases including hypo- or hypertension, heart rate alterations, heart failure, neuronal damage or abnormal skeleton muscle function. In higher eukaryotic organisms, the maintenance of the extracellular [K ] is mainly achieved by the kidney, responsible for K excretion and reabsorption. Thus, renal dysfunctions are typically associated with alterations in serum- or plasma [K ]. Generally, [K ] quantifications within bodily fluids are performed using ion selective electrodes. However, tracking such alterations in experimental models such as mice features several difficulties, mainly due to the small blood volume of these animals, hampering the repetitive collection of sample volumes required for measurements using ion selective electrodes. We have recently developed highly sensitive, genetically encoded potassium ion indicators, the GEPIIs, applicable for in vitro determinations of [K ]. In addition to the determination of [K ] within bodily fluids, GEPIIs proved suitable for the real-time visualization of cell viability over time and the exact determination of the number of dead cells. © 2019 The Authors.

摘要

活细胞维持着跨质膜的陡峭钾离子(K⁺)梯度。细胞内钾离子浓度([K⁺]i),尤其是细胞外基质中的[K⁺]o受到严格调控,后者维持在约3.5至5.0 mM的狭窄范围内。细胞外钾稳态的改变与严重的病理改变和全身性疾病相关,包括低血压或高血压、心率改变、心力衰竭、神经元损伤或骨骼肌功能异常。在高等真核生物中,细胞外[K⁺]o的维持主要通过肾脏来实现,肾脏负责钾的排泄和重吸收。因此,肾功能障碍通常与血清或血浆[K⁺]的改变有关。一般来说,体液中[K⁺]的定量分析是使用离子选择性电极进行的。然而,在小鼠等实验模型中追踪这种变化存在几个困难,主要是由于这些动物的血容量小,妨碍了使用离子选择性电极进行测量所需的重复采集样本量。我们最近开发了高度敏感的、基因编码的钾离子指示剂GEPIIs,适用于体外[K⁺]的测定。除了测定体液中的[K⁺],GEPIIs还被证明适用于实时可视化细胞活力随时间的变化以及准确测定死细胞数量。© 2019作者。

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