| Literature DB >> 31251560 |
Lawrence R Walker1, Elaine M Marzluff2, Julia A Townsend1, William C Resager1, Michael T Marty1.
Abstract
Antimicrobial peptides (AMPs) are generally cationic and amphipathic peptides that show potential applications to combat the growing threat of antibiotic resistant infections. AMPs are known to interact with bacterial membranes, but their mechanisms of toxicity and selectivity are poorly understood, in part because it is challenging to characterize AMP oligomeric complexes within lipid bilayers. Here, we used native mass spectrometry to measure the stoichiometry of AMPs inserted into lipoprotein nanodiscs with different lipid components. Titrations of increasing peptide concentration and collisional activation experiments reveal that AMPs can exhibit a range of behaviors from nonspecific incorporation into the nanodisc to formation of specific complexes. This new approach to characterizing formation of AMP complexes within lipid membranes will provide unique insights into AMP mechanisms.Entities:
Year: 2019 PMID: 31251560 PMCID: PMC6635019 DOI: 10.1021/acs.analchem.9b02261
Source DB: PubMed Journal: Anal Chem ISSN: 0003-2700 Impact factor: 6.986