Computational mechanistic study of human liver glycerol 3‐phosphate dehydrogenase using ONIOM method. (30th June 2020)

• Record Type: Journal Article
• Authors: Yildiz, Ibrahim; Sizirici Yildiz, Banu
• Is Part Of: Journal of physical organic chemistry. Volume 33:Number 11(2020)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2020-06-30
• Subjects: amber -- DFT -- glycerol 3‐phosphate dehydrogenase -- hydride transfer -- NADH; Chemistry, Physical organic -- Periodicals; 547.1
• DOI: 10.1002/poc.4104
• Languages: English
• ISSNs: 0894-3230

Abstract

Abstract: Human liver glycerol 3‐phosphate dehydrogenase catalyzes transfer of a hydride anion from NADH to dihydroxyacetone phosphate (DHAP) forming L‐glycerol 3‐phosphate and NAD + in a single step reaction. It is proposed that a hydride ion is transferred from NADH to the carbonyl carbon of DHAP through a general acid catalysis in which the carbonyl oxygen of DHAP is protonated by a nearby acidic residue. Based on the crystal structure of enzyme, it was suggested that one of the active site lysine residues (Lys120/Lys204) might act as general acid for the protonation of the carbonyl oxygen at DHAP. In this study, we formulated a number of computational systems to study the hydride transfer mechanism including main active site amino acid side chains, NADH cofactor, and DHAP. The calculations involved ONIOM method consisting of DFT and molecular mechanics (MM). We evaluated the energetics of the hydride transfer process in different model systems while probing the roles of active site residues, Lys120/Lys204/Asp260. Based on calculations, protonated Asp260 has more favorable energetics to act as the general acid catalysis as compared to Lys120/204 residues. Abstract : In this study, we employed a hybrid QM‐MM approach using ONIOM method to formulate computational models to analyze geometries and energetics of hydride transfer mechanisms from NADH to DHAP for hlGPDH. Based on calculations, protonated Asp260 has more favorable energetics to act as the general acid catalysis as compared to Lys120/204 residues during the hydride transfer process.