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拟南芥SnRK2.6/OST1:K50N和D160A突变体的克隆、表达、纯化、结晶及初步X射线分析

SnRK2.6/OST1 from Arabidopsis thaliana: cloning, expression, purification, crystallization and preliminary X-ray analysis of K50N and D160A mutants.

作者信息

Yunta Cristina, Martinez-Ripoll Martin, Albert Armando

机构信息

Departamento de Cristalografía y Biología Estructural, Instituto de Química Física Rocasolano, Consejo Superior de Investigaciones Científicas, Serrano 119, 28006 Madrid, Spain.

出版信息

Acta Crystallogr Sect F Struct Biol Cryst Commun. 2011 Mar 1;67(Pt 3):364-8. doi: 10.1107/S1744309110053807. Epub 2011 Feb 25.

Abstract

The SnRK2.6 (SNF1-related kinase 2.6) gene from Arabidopsis thaliana encodes the serine/threonine protein kinase SnRK2.6/OST1 (OPEN STOMATA 1). It plays a central role in the drought-tolerance mechanism. OST1 is in fact the main positive effector in the hydric stress response. The SnRK2.6 gene was cloned into the pGEX4T1 plasmid, mutated and expressed in Escherichia coli, allowing purification to homogeneity in two chromatographic steps. Various OST1 mutants yielded crystals using vapour-diffusion techniques, but only one mutant showed a good diffraction pattern. Its crystals diffracted to 2.8 Å resolution and belonged to space group P222(1), with unit-cell parameters a=77.7, b=99.4, c=108.4 Å. A promising molecular-replacement solution was found using the structure of the kinase domain of the yeast AMP-activated protein kinase SNF1 (PDB entry 3hyh) as the search model.

摘要

来自拟南芥的SnRK2.6(蔗糖非发酵-1相关蛋白激酶2.6)基因编码丝氨酸/苏氨酸蛋白激酶SnRK2.6/OST1(开放气孔1)。它在耐旱机制中起核心作用。事实上,OST1是水分胁迫响应中的主要正向效应因子。SnRK2.6基因被克隆到pGEX4T1质粒中,进行突变并在大肠杆菌中表达,通过两步色谱法可将其纯化至同质状态。使用气相扩散技术,各种OST1突变体都产生了晶体,但只有一个突变体显示出良好的衍射图谱。其晶体衍射分辨率达到2.8 Å,属于空间群P222(1),晶胞参数a=77.7、b=99.4、c=108.4 Å。以酵母AMP激活的蛋白激酶SNF1的激酶结构域结构(PDB登录号3hyh)作为搜索模型,找到了一个有前景的分子置换解决方案。

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