Identification of a Chemical Inhibitor with a Novel Scaffold Targeting Decaprenylphosphoryl-β-D-Ribose Oxidase (DprE1)

Abstract

Background: Tuberculosis is the second leading cause of death from infectious diseases worldwide. Multidrug-resistant Mycobacterium tuberculosis is spreading throughout the world, creating a crisis. Hence, there is a need to develop anti-tuberculosis drugs with novel structures and versatile mechanisms of action. background: Tuberculosis is the second leading cause of death from infectious diseases worldwide. Multidrug-resistant Mycobacterium tuberculosis is spreading throughout the world, creating a crisis situation. There is a need to develop anti-tuberculosis drugs with novel structures that have new mechanisms of action. Objective: In this study, we identified antimicrobial compounds with a novel skeleton that inhibits mycobacterium decaprenylphosphoryl-β-D-ribose oxidase (DprE1). objective: This study aimed to identify antimicrobial compounds with a novel skeleton that inhibits mycobacterium Decaprenylphosphoryl-β-D-ribose oxidase (DprE1). Methods: A multi-step, in silico, structure-based drug screening identified potential DprE1 inhibitors from a library of 154,118 compounds. We experimentally verified the growth inhibitory effects of the eight selected candidate compounds against Mycobacterium smegmatis. Molecular dynamics simulations were performed to understand the mechanism of molecular interactions between DprE1 and ompound 4. Results: Eight compounds were selected through in silico screening. Compound 4 showed strong growth inhibition against M. smegmatis. Molecular dynamics simulation (50 ns) predicted direct and stable binding of Compound 4 to the active site of DprE1. method: A multi-step in silico structure-based drug screening identified potential DprE1 inhibitors from a library of 154,118 compounds. The growth inhibitory effect of the eight selected candidate compounds on Mycobacterium smegmatis was experimentally verified. Molecular dynamics simulations were performed to understand the mechanism of molecular interactions between DprE1 and Compound 4. Conclusion: The structural analysis of the novel scaffold in Compound 4 can pave way for anti-tuberculosis drug development and discovery. other: NA