Drake S K, Zimmer M A, Miller C L, Falke J J
Department of Chemistry and Biochemistry, University of Colorado, Boulder 80309-0215, USA.
Biochemistry. 1997 Aug 12;36(32):9917-26. doi: 10.1021/bi9703913.
In calcium signaling pathways regulated by the EF-hand Ca2+ binding motif, proper regulation requires that the equilibrium and kinetics of Ca2+ binding to the EF-hand chelation loop be precisely optimized for each physiological application. Studies of small-molecule organic chelators have shown that metal binding parameters can be tuned both by the nature of the coordinating ligands and by the structural framework to which these ligands are attached. By analogy, the present study tests the relative importance of (i) coordinating side chains and (ii) backbone torsion angle constraints to the tuning of an EF-hand-like Ca2+ chelation loop. A series of engineered chelation loops are generated by modifying Ca2+ binding site of the Escherichia coli galactose binding protein. The resulting loops, each containing an altered coordinating side chain or a Gly substitution, are compared with respect to their metal binding affinities, specificities, and dissociation kinetics. The Gly variants examined include substitutions which eliminate or introduce a Gly at each of the nine chelation loop positions. The results reveal that Gly is not tolerated at loop positions 1, 3, 5, or 8 or at the external coordinating position, where the removal of a key coordinating or hydrophobic side chain destabilizes the protein. In contrast, Gly residues at loop positions 2, 4, 6, and 7, none of which is required for side chain coordination, have little effect on Ca2+ affinity and the ability to discriminate between cations of different size and charge. Kinetic measurements show that some of these Gly residues measurably alter the rates of metal ion association and dissociation, but in each case the two rates are changed by approximately the same factor so that the effects on equilibrium are minor. Overall, Gly residues yield surprisingly small effects at loop positions 2, 4, 6, and 7, especially when compared to the larger equilibrium and kinetic effects observed for coordinating side chain substitutions. It follows that the conserved Gly at position 6 is not required for Ca2+ binding and that constraints on the backbone torsion angles at the non-coordinating side chain positions 2, 4, 6, and 7 play a relatively minor role in tuning metal binding parameters. Instead, specific coordinating side chains optimize the metal binding parameters of the GBP chelation loop for its protein context and biological application.
在由EF手型Ca²⁺结合基序调控的钙信号通路中,恰当的调控要求Ca²⁺与EF手型螯合环结合的平衡和动力学针对每种生理应用精确优化。对小分子有机螯合剂的研究表明,金属结合参数可以通过配位配体的性质以及这些配体所连接的结构框架来调节。以此类推,本研究测试了(i)配位侧链和(ii)主链扭转角限制对类EF手型Ca²⁺螯合环调节的相对重要性。通过修饰大肠杆菌半乳糖结合蛋白的Ca²⁺结合位点,生成了一系列工程化的螯合环。将所得的环,每个都含有一个改变的配位侧链或一个甘氨酸取代,就其金属结合亲和力、特异性和解离动力学进行比较。所研究的甘氨酸变体包括在九个螯合环位置中的每个位置消除或引入一个甘氨酸的取代。结果表明,在环位置1、3、5或8或外部配位位置,甘氨酸是不能被容忍的,在这些位置去除关键的配位或疏水侧链会使蛋白质不稳定。相比之下,环位置2、4、6和7处的甘氨酸残基,其侧链配位并非必需,对Ca²⁺亲和力以及区分不同大小和电荷阳离子的能力几乎没有影响。动力学测量表明,其中一些甘氨酸残基可显著改变金属离子结合和解离的速率,但在每种情况下,这两个速率的变化因子大致相同,因此对平衡的影响较小。总体而言,甘氨酸残基在环位置2、4、6和7处产生的影响惊人地小,特别是与配位侧链取代所观察到的更大的平衡和动力学效应相比。由此可见,位置6处保守的甘氨酸对于Ca²⁺结合并非必需,并且在非配位侧链位置2、4、6和7处对主链扭转角的限制在调节金属结合参数方面起相对较小的作用。相反,特定的配位侧链针对其蛋白质环境和生物学应用优化了GBP螯合环的金属结合参数。