基于质谱法的体外Kinome底物发现。

Q3 Physics and Astronomy
Mass spectrometry Pub Date : 2020-01-01 Epub Date: 2020-03-28 DOI:10.5702/massspectrometry.A0082
Naoyuki Sugiyama
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引用次数: 3

摘要

蛋白激酶介导的蛋白磷酸化是许多生物学事件中最重要的翻译后修饰之一。特定蛋白激酶的功能和生理底物与已知的信号转导元件或治疗靶点高度相关,已经通过各种方法进行了广泛的研究;然而,大多数蛋白激酶尚未被表征。近几十年来,已经开发了许多技术来鉴定蛋白激酶的体外和生理底物。在这篇综述中,我总结了最近使用基于质谱的蛋白质组学分析激酶特征的研究,重点是使用定量磷酸化蛋白质组学方法对人类激酶的体外底物进行大规模鉴定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Mass Spectrometry-Based Discovery of <i>in vitro</i> Kinome Substrates.

Mass Spectrometry-Based Discovery of <i>in vitro</i> Kinome Substrates.

Mass Spectrometry-Based Discovery of <i>in vitro</i> Kinome Substrates.

Mass Spectrometry-Based Discovery of in vitro Kinome Substrates.

Protein phosphorylation mediated by protein kinases is one of the most significant posttranslational modifications in many biological events. The function and physiological substrates of specific protein kinases, which are highly associated with known signal transduction elements or therapeutic targets, have been extensively studied using various approaches; however, most protein kinases have not yet been characterized. In recent decades, many techniques have been developed for the identification of in vitro and physiological substrates of protein kinases. In this review, I summarize recent studies profiling the characteristics of kinases using mass spectrometry-based proteomics, focusing on the large-scale identification of in vitro substrates of the human kinome using a quantitative phosphoproteomics approach.

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来源期刊
Mass spectrometry
Mass spectrometry Physics and Astronomy-Instrumentation
CiteScore
1.90
自引率
0.00%
发文量
3
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