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一种简单的体外方法来测量蛋白激酶的自动磷酸化。

A simple in vitro method to measure autophosphorylation of protein kinases.

机构信息

Division of Biological Sciences, University of Missouri, Columbia, MO 65211, USA.

出版信息

Plant Methods. 2013 Jun 26;9(1):22. doi: 10.1186/1746-4811-9-22.

Abstract

Receptor-like protein kinases (RLKs) are a large and important group of plant proteins involved in numerous aspects of development and stress response. Within this family, homo-oligermization of receptors followed by autophosphorylation of the intracellular protein kinase domain appears to be a widespread mechanism to regulate protein kinase activity. In vitro studies of several RLKs have identified autophosphorylation sites involved in regulation of catalytic activity and signaling in vivo. Recent work has established that multiple RLKs are biochemically active when expressed in E. coli and readily autophosphorylate prior to purification or subsequent manipulation. This observation has led us to develop a simplified method for assaying RLK phosphorylation status as an indirect measure of intrinsic autophosphorylation activity. The method involves expressing a recombinant RLK protein kinase domain in E. coli, followed by SDS-PAGE of boiled cell lysate, and sequential staining with the phosphoprotein stain Pro-Q Diamond and a colloidal Coomassie total protein stain. We show this method can be used to measure and quantify in vitro autophosphorylation levels of recombinant wildtype and mutant versions of the Arabidopsis RLK HAESA, as well as to detect transphosphorylation activity of recombinant HAESA against a protein kinase inactive version of itself. Our method has several advantages over traditional protein kinase assays. It does not require protein purification, transfer, blotting, or radioactive reagents. It allows for rapid and quantitative assessment of autophosphorylation levels and should have general utility in the study of any autophosphorylating protein kinase expressed in E. coli.

摘要

受体样蛋白激酶(RLKs)是一大类重要的植物蛋白,参与了发育和应激反应的多个方面。在这个家族中,受体的同源寡聚化,随后是细胞内蛋白激酶结构域的自磷酸化,似乎是一种广泛存在的调节蛋白激酶活性的机制。对几种 RLKs 的体外研究已经确定了参与体内催化活性和信号转导调节的自磷酸化位点。最近的工作表明,当在大肠杆菌中表达时,多个 RLKs 在纯化前或后续操作前就具有生物化学活性,并且容易发生自磷酸化。这一观察结果促使我们开发了一种简化的方法来检测 RLK 的磷酸化状态,作为内在自磷酸化活性的间接测量。该方法涉及在大肠杆菌中表达重组 RLK 蛋白激酶结构域,然后煮沸细胞裂解物进行 SDS-PAGE,并用磷酸蛋白染色剂 Pro-Q Diamond 和胶体考马斯亮蓝总蛋白染色剂进行连续染色。我们表明,该方法可用于测量和定量体外重组拟南芥 RLK HAESA 的野生型和突变体版本的自磷酸化水平,以及检测重组 HAESA 对自身蛋白激酶失活版本的转磷酸化活性。与传统的蛋白激酶测定方法相比,我们的方法具有几个优点。它不需要蛋白纯化、转移、印迹或放射性试剂。它允许快速和定量评估自磷酸化水平,并且应该在研究任何在大肠杆菌中表达的自磷酸化蛋白激酶中具有普遍的应用价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c7e9/3702502/56a28df21609/1746-4811-9-22-1.jpg

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