Revealing quantum mechanical effects in enzyme catalysis with large-scale electronic structure simulation. Issue 2 (6th December 2018)

• Record Type: Journal Article
• Authors: Yang, Zhongyue; Mehmood, Rimsha; Wang, Mengyi; Qi, Helena W.; Steeves, Adam H.; Kulik, Heather J.
• Is Part Of: Reaction chemistry & engineering. Volume 4:Issue 2(2019)
• Page Start: 298
• Page End: 315
• Publication Date: 2018-12-06
• Subjects: Reaction mechanisms (Chemistry) -- Periodicals; Chemical engineering -- Periodicals; Chemical engineering; Reaction mechanisms (Chemistry); Periodicals; 547.705
• DOI: 10.1039/c8re00213d
• Languages: English
• ISSNs: 2058-9883

Abstract

Abstract : Large scale quantum mechanical simulation systematically reveals length scales over which electronically driven interactions occur at enzyme active sites. Abstract : Enzymes have evolved to facilitate challenging reactions at ambient conditions with specificity seldom matched by other catalysts. Computational modeling provides valuable insight into catalytic mechanism, and the large size of enzymes mandates multi-scale, quantum mechanical-molecular mechanical (QM/MM) simulations. Although QM/MM plays an essential role in balancing simulation cost to enable sampling with the full QM treatment needed to understand electronic structure in enzyme active sites, the relative importance of these two strategies for understanding enzyme mechanism is not well known. We explore challenges in QM/MM for studying the reactivity and stability of three diverse enzymes: i) Mg 2+ -dependent catechol O -methyltransferase (COMT), ii) radical enzyme choline trimethylamine lyase (CutC), and iii) DNA methyltransferase (DNMT1), which has structural Zn 2+ binding sites. In COMT, strong non-covalent interactions lead to long range coupling of electronic structure properties across the active site, but the more isolated nature of the metallocofactor in DNMT1 leads to faster convergence of some properties. We quantify these effects in COMT by computing covariance matrices of by-residue electronic structure properties during dynamics and along the reaction coordinate. In CutC, we observe spontaneous bond cleavage following initiation events, highlighting the importance of sampling and dynamics. We use electronic structure analysis to quantify the relative importance of CHO and OHO non-covalent interactions in imparting reactivity. These three diverse cases enable us to provide some general recommendations regarding QM/MM simulation of enzymes.