State Key Laboratory of Microbial Metabolism, Joint International Research Laboratory of Metabolic and Developmental Sciences, School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai 200240, China.
Int J Mol Sci. 2019 Feb 18;20(4):877. doi: 10.3390/ijms20040877.
As a polyene antibiotic of great pharmaceutical significance, pimaricin has been extensively studied to enhance its productivity and effectiveness. In our previous studies, pre-reaction state (PRS) has been validated as one of the significant conformational categories before macrocyclization, and is critical to mutual recognition and catalytic preparation in thioesterase (TE)-catalyzed systems. In our study, molecular dynamics (MD) simulations were conducted on pimaricin TE-polyketide complex and PRS, as well as pre-organization state (POS), a molecular conformation possessing a pivotal intra-molecular hydrogen bond, were detected. Conformational transition between POS and PRS was observed in one of the simulations, and POS was calculated to be energetically more stable than PRS by 4.58 kcal/mol. The structural characteristics of PRS and POS-based hydrogen-bonding, and hydrophobic interactions were uncovered, and additional simulations were carried out to rationalize the functions of several key residues (Q29, M210, and R186). Binding energies, obtained from MM/PBSA calculations, were further decomposed to residues, in order to reveal their roles in product release. Our study advanced a comprehensive understanding of pimaricin TE-catalyzed macrocyclization from the perspectives of conformational change, protein-polyketide recognition, and product release, and provided potential residues for rational modification of pimaricin TE.
作为一种具有重要医药意义的多烯抗生素,制霉菌素的生产效率和效果得到了广泛的研究。在我们之前的研究中,预反应态(PRS)被验证为大环化前的重要构象类别之一,对于硫酯酶(TE)催化体系中的相互识别和催化准备至关重要。在我们的研究中,对制霉菌素 TE-聚酮复合物和 PRS 进行了分子动力学(MD)模拟,并检测到预组织态(POS),这是一种具有关键分子内氢键的分子构象。在一次模拟中观察到 POS 和 PRS 之间的构象转变,并且通过 4.58 kcal/mol 的能量计算发现 POS 比 PRS 更稳定。揭示了 PRS 和 POS 基于氢键和疏水相互作用的结构特征,并进行了额外的模拟以合理化几个关键残基(Q29、M210 和 R186)的功能。通过 MM/PBSA 计算获得的结合能进一步分解到残基上,以揭示它们在产物释放中的作用。我们的研究从构象变化、蛋白质-聚酮识别和产物释放的角度推进了对制霉菌素 TE 催化大环化的全面理解,并为制霉菌素 TE 的合理修饰提供了潜在的残基。