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定义编码激酶、磷酸转移和CheY结合活性结构域的CheA片段的表达。

Expression of CheA fragments which define domains encoding kinase, phosphotransfer, and CheY binding activities.

作者信息

Swanson R V, Schuster S C, Simon M I

机构信息

Division of Biology, California Institute of Technology, Pasadena 91125.

出版信息

Biochemistry. 1993 Aug 3;32(30):7623-9. doi: 10.1021/bi00081a004.

DOI:10.1021/bi00081a004
PMID:8347572
Abstract

The histidine protein kinase CheA is a central component of the Escherichia coli chemotaxis system. The autophosphorylation activity of CheA is controlled by membrane-bound chemoreceptors and by the CheW coupling protein. CheA phosphorylates the CheY and CheB proteins which respectively control the direction of flagellar rotation and the level of receptor adaptation, thereby regulating the cells' chemotactic response. Genes encoding three polypeptide fragments of CheA were constructed and expressed in order to better define the functional organization of the wild-type protein. These fragments allowed the identification of regions of the protein responsible for CheY binding, phosphotransfer, and kinase activity. The kinase domain was expressed as a 30-kDa polypeptide corresponding to the central portion of the wild-type protein which contains sequences homologous to other histidine kinases. It was able to phosphorylate a 15-kDa amino-terminal phosphotransfer domain which was separately expressed and purified. This latter domain is capable of phosphotransfer to CheY despite the fact that it lacks the ability to stably bind CheY. CheY was immobilized to a dextran matrix through a single cysteine residue which was introduced into the protein at a position far removed from the active site. A stable binding site for CheY was mapped to a segment between the site of autophosphorylation and the kinase domain by using surface plasmon resonance to detect binding to the immobilized CheY. The region of the kinase which tightly binds the unphosphorylated substrate may play an important role in regulating the specificity of the signal transducing system.

摘要

组氨酸蛋白激酶CheA是大肠杆菌趋化系统的核心组成部分。CheA的自磷酸化活性受膜结合化学感受器和CheW偶联蛋白的控制。CheA使CheY和CheB蛋白磷酸化,它们分别控制鞭毛旋转方向和受体适应水平,从而调节细胞的趋化反应。构建并表达了编码CheA三个多肽片段的基因,以便更好地确定野生型蛋白的功能组织。这些片段有助于鉴定该蛋白中负责与CheY结合、磷酸转移和激酶活性的区域。激酶结构域作为一种30 kDa的多肽表达,对应于野生型蛋白的中央部分,其中包含与其他组氨酸激酶同源的序列。它能够使单独表达和纯化的15 kDa氨基末端磷酸转移结构域磷酸化。尽管后者缺乏稳定结合CheY的能力,但它能够将磷酸转移给CheY。通过将一个半胱氨酸残基引入到远离活性位点的位置,使CheY固定在葡聚糖基质上。利用表面等离子体共振检测与固定化CheY的结合,将CheY的一个稳定结合位点定位到自磷酸化位点和激酶结构域之间的一段区域。激酶中紧密结合未磷酸化底物的区域可能在调节信号转导系统的特异性方面发挥重要作用。

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Biochemistry. 1993 Aug 3;32(30):7623-9. doi: 10.1021/bi00081a004.
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