Pelc Leslie A, Chen Zhiwei, Gohara David W, Vogt Austin D, Pozzi Nicola, Di Cera Enrico
Edward A. Doisy Department of Biochemistry and Molecular Biology, Saint Louis University School of Medicine , St. Louis, Missouri 63104, United States.
Biochemistry. 2015 Feb 24;54(7):1457-64. doi: 10.1021/acs.biochem.5b00014. Epub 2015 Feb 11.
Although Thr is equally represented as Ser in the human genome and as a nucleophile is as good as Ser, it is never found in the active site of the large family of trypsin-like proteases that utilize the Asp/His/Ser triad. The molecular basis of the preference of Ser over Thr in the trypsin fold was investigated with X-ray structures of the thrombin mutant S195T free and bound to an irreversible active site inhibitor. In the free form, the methyl group of T195 is oriented toward the incoming substrate in a conformation seemingly incompatible with productive binding. In the bound form, the side chain of T195 is reoriented for efficient substrate acylation without causing steric clash within the active site. Rapid kinetics prove that this change is due to selection of an active conformation from a preexisting ensemble of reactive and unreactive rotamers whose relative distribution determines the level of activity of the protease. Consistent with these observations, the S195T substitution is associated with a weak yet finite activity that allows identification of an unanticipated important role for S195 as the end point of allosteric transduction in the trypsin fold. The S195T mutation abrogates the Na(+)-dependent enhancement of catalytic activity in thrombin, activated protein C, and factor Xa and significantly weakens the physiologically important allosteric effects of thrombomodulin on thrombin and of cofactor Va on factor Xa. The evolutionary selection of Ser over Thr in trypsin-like proteases was therefore driven by the need for high catalytic activity and efficient allosteric regulation.
虽然在人类基因组中苏氨酸(Thr)与丝氨酸(Ser)的含量相当,并且作为亲核试剂与丝氨酸一样出色,但在利用天冬氨酸/组氨酸/丝氨酸三联体的一大类胰蛋白酶样蛋白酶的活性位点中从未发现过苏氨酸。通过凝血酶突变体S195T游离态和与不可逆活性位点抑制剂结合态的X射线结构,研究了胰蛋白酶折叠中丝氨酸优于苏氨酸的分子基础。在游离形式下,T195的甲基以一种似乎与有效结合不相容的构象朝向进入的底物。在结合形式下,T195的侧链重新定向以实现有效的底物酰化,而不会在活性位点内引起空间冲突。快速动力学证明这种变化是由于从预先存在的反应性和非反应性旋转异构体集合中选择了一种活性构象,其相对分布决定了蛋白酶的活性水平。与这些观察结果一致,S195T取代与微弱但有限的活性相关,这使得能够确定S195作为胰蛋白酶折叠中变构转导终点的意外重要作用。S195T突变消除了凝血酶、活化蛋白C和因子Xa中钠离子依赖性的催化活性增强,并显著削弱了凝血调节蛋白对凝血酶以及辅因子Va对因子Xa的生理重要变构效应。因此,胰蛋白酶样蛋白酶中丝氨酸优于苏氨酸的进化选择是由对高催化活性和有效变构调节的需求驱动的。