Live-cell Imaging with Genetically Encoded Protein Kinase Activity Reporters.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
ACS Applied Bio Materials Pub Date : 2018-04-25 Epub Date: 2018-03-17 DOI:10.1247/csf.18003
Gembu Maryu, Haruko Miura, Youichi Uda, Akira T Komatsubara, Michiyuki Matsuda, Kazuhiro Aoki
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引用次数: 21

Abstract

Protein kinases play pivotal roles in intracellular signal transduction, and dysregulation of kinases leads to pathological results such as malignant tumors. Kinase activity has hitherto been measured by biochemical methods such as in vitro phosphorylation assay and western blotting. However, these methods are less useful to explore spatial and temporal changes in kinase activity and its cell-to-cell variation. Recent advances in fluorescent proteins and live-cell imaging techniques enable us to visualize kinase activity in living cells with high spatial and temporal resolutions. Several genetically encoded kinase activity reporters, which are based on the modes of action of kinase activation and phosphorylation, are currently available. These reporters are classified into single-fluorophore kinase activity reporters and Förster (or fluorescence) resonance energy transfer (FRET)-based kinase activity reporters. Here, we introduce the principles of genetically encoded kinase activity reporters, and discuss the advantages and disadvantages of these reporters.Key words: kinase, FRET, phosphorylation, KTR.

基因编码蛋白激酶活性报告基因的活细胞成像。
蛋白激酶在细胞内信号转导中起着关键作用,激酶的失调会导致恶性肿瘤等病理结果。迄今为止,激酶活性一直是通过体外磷酸化测定和western blotting等生化方法来测定的。然而,这些方法在探索激酶活性的时空变化及其细胞间变异方面用处不大。荧光蛋白和活细胞成像技术的最新进展使我们能够以高空间和时间分辨率可视化活细胞中的激酶活性。目前已有几种基于激酶活化和磷酸化作用模式的基因编码激酶活性报告基因。这些报告分为单荧光团激酶活性报告和Förster(或荧光)共振能量转移(FRET)为基础的激酶活性报告。在这里,我们介绍了基因编码激酶活性报告基因的原理,并讨论了这些报告基因的优缺点。关键词:激酶,FRET,磷酸化,KTR。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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