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前沿:一种用于分析调控T细胞发育的激酶的化学遗传系统。

Cutting edge: a chemical genetic system for the analysis of kinases regulating T cell development.

作者信息

Denzel Angela, Hare Katherine J, Zhang Chao, Shokat Kevan, Jenkinson Eric J, Anderson Graham, Hayday Adrian

机构信息

Department of Immunobiology, New Guy's House, Guy's, King's and St. Thomas's School of Medicine, London, United Kingdom.

出版信息

J Immunol. 2003 Jul 15;171(2):519-23. doi: 10.4049/jimmunol.171.2.519.

Abstract

To understand the regulatory activities of kinases in vivo requires their study across a biologically relevant window of activity. To this end, ATP analog-sensitive kinase alleles (ASKAs) specifically sensitive to a competitive inhibitor have been developed. This article tests whether ASKA technology can be applied to complex immunological systems, such as lymphoid development. The results show that when applied to reaggregate thymic organ culture, novel p56(Lck) ASKAs readily expose a dose-dependent correlation of thymocyte development with a range of p56(Lck) activity. By regulating kinase activity, rather than amounts of RNA or protein, ASKA technology offers a general means for assessing the quantitative contributions to immunology of numerous kinases emerging from genomics analyses. It can obviate the generation of multiple lines of mice expressing different levels of kinase transgenes and should permit specific biological effects to be associated with defined biochemical activities.

摘要

要了解激酶在体内的调节活性,需要在生物学相关的活性窗口内对其进行研究。为此,已经开发出了对竞争性抑制剂具有特异性敏感性的ATP类似物敏感激酶等位基因(ASKAs)。本文测试了ASKA技术是否可应用于复杂的免疫系统,如淋巴细胞发育。结果表明,当应用于重组胸腺器官培养时,新型p56(Lck)ASKAs很容易揭示胸腺细胞发育与一系列p56(Lck)活性之间的剂量依赖性相关性。通过调节激酶活性,而不是RNA或蛋白质的量,ASKA技术提供了一种通用方法,用于评估基因组分析中出现的众多激酶对免疫学的定量贡献。它可以避免产生多条表达不同水平激酶转基因的小鼠品系,并且应该能够将特定的生物学效应与明确的生化活性联系起来。

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