ePrints@IIScePrints@IISc Home | About | Browse | Latest Additions | Advanced Search | Contact | Help

A Peptide-Nanoparticle System with Improved Efficacy against Multidrug Resistant Bacteria

Pal, I and Bhattacharyya, D and Kar, RK and Zarena, D and Bhunia, A and Atreya, HS (2019) A Peptide-Nanoparticle System with Improved Efficacy against Multidrug Resistant Bacteria. In: Scientific Reports, 9 (1).

[img]
Preview
PDF
Sci_Rep_9_1_2019.pdf - Published Supplemental Material

Download (5MB) | Preview
[img] Microsoft Word
41598_2019_41005_MOESM2_ESM.docx - Published Supplemental Material

Download (3MB)
Official URL: https://doi.org/10.1038/s41598-019-41005-7

Abstract

The recent rise of multidrug resistant microbial strains requires development of new and novel therapeutic alternatives. In this study, we present a novel antibacterial system that comprises of modified naturally abundant antimicrobial peptides in conjugation with silver nanoparticles. Further, we propose a simple route to incorporate a cysteine residue either at the N- or C-terminal of the parent peptide. Tagging a cysteine residue at the terminals not only enhances the binding propensity of the resultant peptide with the silver nanoparticle, but also increases its antimicrobial property against several pathogenic bacterial strains including K. pneumoniae. The minimum inhibitory concentration (MIC) values of the cysteine tagged nanoconjugates were obtained in the range of 5�15 μM compared to 50 μM for peptides devoid of the cysteines. The origin and mechanism of such improved activity of the conjugates were investigated using NMR spectroscopy and molecular dynamics (MD) simulations. The application of 13 C-isotope labelled media to track the metabolic lifecycle of E. coli cells provided further insights into the system. MD simulations showed that pore formation in membrane bilayer is mediated through a hydrophobic collapse mechanism. The design strategy described herein opens up new-avenues for using biocompatible nanomedicines as a potential alternative to conventional antibiotics. © 2019, The Author(s).

Item Type: Journal Article
Publication: Scientific Reports
Publisher: Nature Publishing Group
Department/Centre: Division of Chemical Sciences > NMR Research Centre (Formerly Sophisticated Instruments Facility)
Date Deposited: 22 Apr 2019 07:40
Last Modified: 22 Apr 2019 07:50
URI: http://eprints.iisc.ac.in/id/eprint/62132

Actions (login required)

View Item View Item