| Literature DB >> 32175733 |
Venkatesh Mayandi1,2, Qingxiao Xi1, Eunice Tze Leng Goh1, Siew Kwan Koh3, Thomas Yong Jie Toh1, Veluchamy Amutha Barathi1,4,5, Mobashar Hussain Urf Turabe Fazil6, Madhavi Latha Somaraju Chalasani6, Jayasudha Varadarajan1, Darren Shu Jeng Ting1,7, Roger W Beuerman1,5, Lai Wah Chan8, Rupesh Agrawal9, Timothy Mark Sebastian Barkham10, Lei Zhou3,4,5, Navin Kumar Verma1,6,11, Rajamani Lakshminarayanan1,5,8.
Abstract
Here, we present a rational approach that enhances the membrane selectivity of a prolific pore-forming peptide, melittin, based on experimental observations that the cationic polymer, ε-polylysine, disrupts bacterial membranes with greater affinity over mammalian cells when compared to poly-l-lysine and poly-d-lysine. We systematically replaced three α-lysine residues in melittin with ε-lysine residues and identified key residues that are important for cytotoxicity. We then assessed the antimicrobial properties of the modified peptides which carry two or three ε-lysyl residues. Two modified melittin peptides displayed rapid bactericidal properties against antibiotic-resistant strains, low innate resistance development by pathogenic bacteria, remained nonimmunogenic for T lymphocytes, and increased bioavailability in tear fluids. In proof-of-concept in vivo experiments, one of the peptides was noncytotoxic for ocular surfaces and had comparable antimicrobial efficacy to that of fluoroquinolone antibiotics. The results uncover a simple and potential strategy that can enhance the membrane selectivity of cytolytic peptides by ε-lysylation.Entities:
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Year: 2020 PMID: 32175733 DOI: 10.1021/acs.jmedchem.9b01846
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446