Membrane adsorption enhances translocation of antimicrobial peptide buforin 2

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14740%2F23%3A00132213" target="_blank" >RIV/00216224:14740/23:00132213 - isvavai.cz</a>

Výsledek na webu

<a href="https://mkon.nu/ebsa/scientific_program" target="_blank" >https://mkon.nu/ebsa/scientific_program</a>

DOI - Digital Object Identifier

—

Jazyk výsledku

angličtina

Název v původním jazyce

Membrane adsorption enhances translocation of antimicrobial peptide buforin 2

Popis výsledku v původním jazyce

Antibiotic resistance has been identified as one of the top three threats to human public health. Promising alternatives to antibiotics are antimicrobial peptides (AMPs) that can selectively kill bacterial cells. Buforin 2 (BF2) is an AMP that kills bacteria via intracellular interactions rather than membrane lysis. BF2 membrane translocation is known to be independent of any cellular receptor because BF2 can readily enter bacterial cells and vesicles that contain only lipids in their membrane. However, the free energy barrier for BF2 translocation across a symmetric membrane suggests a non-spontaneous process, demonstrating our poor understanding of the molecular details of how BF2 crosses biological membranes. Here, we show that inducing membrane asymmetry by BF2 adsorption on one leaflet significantly enhances BF2 translocation across bilayers, indicating that membrane asymmetry may act as a driving force for membrane transport. Our results shed light on the crowding effect of AMP on antibacterial activity and are expected to be helpful in the design of new AMPs.

Název v anglickém jazyce

Membrane adsorption enhances translocation of antimicrobial peptide buforin 2

Popis výsledku anglicky

Antibiotic resistance has been identified as one of the top three threats to human public health. Promising alternatives to antibiotics are antimicrobial peptides (AMPs) that can selectively kill bacterial cells. Buforin 2 (BF2) is an AMP that kills bacteria via intracellular interactions rather than membrane lysis. BF2 membrane translocation is known to be independent of any cellular receptor because BF2 can readily enter bacterial cells and vesicles that contain only lipids in their membrane. However, the free energy barrier for BF2 translocation across a symmetric membrane suggests a non-spontaneous process, demonstrating our poor understanding of the molecular details of how BF2 crosses biological membranes. Here, we show that inducing membrane asymmetry by BF2 adsorption on one leaflet significantly enhances BF2 translocation across bilayers, indicating that membrane asymmetry may act as a driving force for membrane transport. Our results shed light on the crowding effect of AMP on antibacterial activity and are expected to be helpful in the design of new AMPs.

Druh

O - Ostatní výsledky

CEP obor

—

OECD FORD obor

10608 - Biochemistry and molecular biology

Projekt

<a href="/cs/project/LX22NPO5103" target="_blank" >LX22NPO5103: Národní institut virologie a bakteriologie</a><br>

Návaznosti

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Rok uplatnění

2023

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů