The Riddet Institute, Palmerston North, New Zealand.
Biophys J. 2013 Apr 16;104(8):1731-9. doi: 10.1016/j.bpj.2013.02.049.
The dynamical behavior of biomacromolecules is a fundamental property regulating a large number of biological processes. Protein dynamics have been widely shown to play a role in enzyme catalysis; however, the interplay between substrate dynamics and enzymatic activity is less understood. We report insights into the role of dynamics of substrates in the enzymatic activity of PME from Erwinia chrysanthemi, a processive enzyme that catalyzes the hydrolysis of methylester groups from the galacturonic acid residues of homogalacturonan chains, the major component of pectin. Extensive molecular dynamics simulations of this PME in complex with decameric homogalacturonan chains possessing different degrees and patterns of methylesterification show how the carbohydrate substitution pattern governs the dynamics of the substrate in the enzyme's binding cleft, such that substrate dynamics represent a key prerequisite for the PME biological activity. The analyses reveal that correlated rotations around glycosidic bonds of monosaccharide subunits at and immediately adjacent to the active site are a necessary step to ensure substrate processing. Moreover, only substrates with the optimal methylesterification pattern attain the correct dynamical behavior to facilitate processive catalysis. This investigation is one of the few reported examples of a process where the dynamics of a substrate are vitally important.
生物大分子的动力学行为是调节许多生物过程的基本性质。蛋白质动力学已被广泛证明在酶催化中起作用;然而,底物动力学和酶活性之间的相互作用还不太清楚。我们报告了对果胶主要成分半乳糖醛酸残基甲酯基团水解的连续酶 Erwinia chrysanthemi 中的 PME 酶活性中底物动力学作用的深入了解。该 PME 与具有不同程度和模式甲酯化的十聚体同源半乳糖醛酸链的复合物的广泛分子动力学模拟表明,碳水化合物取代模式如何控制酶结合裂缝中底物的动力学,使得底物动力学成为 PME 生物学活性的关键前提。分析表明,位于和紧邻活性位点的单糖亚基的糖苷键周围的相关旋转是确保底物加工的必要步骤。此外,只有具有最佳甲酯化模式的底物才能获得正确的动力学行为,从而促进连续催化。这项研究是少数报道的底物动力学至关重要的过程之一。