Rational targeting of Wzb phosphatase and Wzc kinase interaction inhibits extracellular polysaccharides synthesis and biofilm formation in Acinetobacter baumannii. (June 2020)

• Record Type: Journal Article
• Authors: Tiwari, Monalisa; Panwar, Shruti; Kothidar, Akansha; Tiwari, Vishvanath
• Is Part Of: Carbohydrate research. Volume 492(2020)
• Publication Date: 2020-06
• Subjects: Acinetobacter baumannii -- Wzb-wzc interaction -- Wzb protein -- Wzc protein -- Tyrosine kinase -- Tyrosine phosphatase -- Exopolysaccharides -- Antibiotics -- Membrane proteins -- Biofilm; Carbohydrates -- Periodicals; Chemistry, Organic -- Periodicals; Biochemistry -- Periodicals; Carbohydrates -- Periodicals; Chimie organique -- Périodiques; Glucides -- Périodiques; Biochemistry; Carbohydrates; Chemistry, Organic; Periodicals; Electronic journals; 507.78
• DOI: 10.1016/j.carres.2020.108025
• Languages: English
• ISSNs: 0008-6215

Abstract

Abstract: Acinetobacter baumannii is an opportunistic nosocomial pathogen, and responsible for high mortality and morbidity. Biofilm formation is one of the resistance determinants, where extracellular polysaccharide (EPS) is an essential component. EPS synthesis and its export is regulated by the bacterial Wza-Wzb-Wzc system. Wzc exhibits auto-phosphorylation protein tyrosine kinase activity, while Wzb is a protein tyrosine phosphatase. Wzb mediates dephosphorylation of Wzc. Dephosphorylated Wzc is required for the export of the EPS through porin Wza-Wzc complex. It shows that the interaction of Wzb with Wzc is critical for the export of EPS. Therefore, if the Wzb-Wzc interaction is inhibited, then it might hinder the EPS transport and diminish the biofilm formation. In this study, we have modelled the Wzb, and Wzc proteins and further validated using PSVS, ProSA, RAMPAGE, and PDBsum. The modelled proteins were used for protein-protein docking. The docked protein-protein complex was minimized by Schrodinger software using OPLS_2005 force field. The binding site of the minimized Wzb-Wzc complex was identified by Sitemap. The high throughput virtual screening identified Labetalol hydrochloride and 4-{1-hydroxy-2-[(1-methyl-3-phenylpropyl) amino] propyl} phenol from FDA-approved drug library based on their interaction at the interface of Wzb-Wzc complex. The inhibitor-protein complex was further undergone molecular mechanics analysis using Generalized Born model and Solvent Accessibility (MMGBSA) to estimate the binding free energies. The lead was also used to generate the pharmacophore model and screening the molecule with antimicrobial scaffold. The identified lead was experimentally validated for its effect on EPS quantity and biofilm formation by A. baumannii . Wzb-Wzc interaction is essential for biofilm and EPS export; hence, the identified lead might be useful to regulate the biofilm formation by A. baumannii . Graphical abstract: Image 1 Highlights: EPS synthesis and its export in A. baumannii is regulated by the bacterial Wza-Wzb-Wzc system. Dephosphorylated Wzc is required for the export of the EPS through porin Wza-Wzc complex. Labetalol hydrochloride and 4-{1-hydroxy-2-[(1-methyl-3-phenylpropyl)amino] propyl} phenol bind at interface of complex. Pharmacophore model was generated for lead and screening the molecule with antimicrobial scaffold. Lead was experimentally validated for its effect on EPS quantity and biofilm formation by A. baumannii.