Rationally designed foldameric adjuvants enhance antibiotic efficacy


Journal

Molecular systems design & engineering
ISSN: 2058-9689
Titre abrégé: Mol Syst Des Eng
Pays: England
ID NLM: 101683399

Informations de publication

Date de publication:
04 Jan 2022
Historique:
received: 17 08 2021
accepted: 06 10 2021
entrez: 7 2 2022
pubmed: 8 2 2022
medline: 8 2 2022
Statut: epublish

Résumé

The negative membrane potential of bacterial cells influences crucial cellular processes. Inspired by the molecular scaffold of the antimicrobial peptide PGLa, we have developed antimicrobial foldamers with a computer-guided design strategy. The novel PGLa analogues induce sustained membrane hyperpolarization. When co-administered as an adjuvant, the resulting compounds - PGLb1 and PGLb2 - have substantially reduced the level of antibiotic resistance of multi-drug resistant

Identifiants

pubmed: 35127141
doi: 10.1039/d1me00118c
pii: d1me00118c
pmc: PMC8724909
doi:

Types de publication

Journal Article

Langues

eng

Pagination

21-33

Informations de copyright

This journal is © The Royal Society of Chemistry.

Déclaration de conflit d'intérêts

There are no conflicts to declare.

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Auteurs

Kaushik Nath Bhaumik (KN)

Department of Medical Chemistry, University of Szeged Dóm tér 8 Szeged HU-6720 Hungary martinek.tamas@med.u-szeged.hu.

Anasztázia Hetényi (A)

Department of Medical Chemistry, University of Szeged Dóm tér 8 Szeged HU-6720 Hungary martinek.tamas@med.u-szeged.hu.

Gábor Olajos (G)

Department of Medical Chemistry, University of Szeged Dóm tér 8 Szeged HU-6720 Hungary martinek.tamas@med.u-szeged.hu.

Ana Martins (A)

Synthetic and Systems Biology Unit, Biological Research Centre, Eötvös Loránd Research Network (ELKH) Szeged Hungary.

Réka Spohn (R)

Synthetic and Systems Biology Unit, Biological Research Centre, Eötvös Loránd Research Network (ELKH) Szeged Hungary.

Lukács Németh (L)

Institute of Food Engineering, University of Szeged Szeged Hungary.

Balázs Jojart (B)

Institute of Food Engineering, University of Szeged Szeged Hungary.

Petra Szili (P)

Synthetic and Systems Biology Unit, Biological Research Centre, Eötvös Loránd Research Network (ELKH) Szeged Hungary.
Doctoral School of Multidisciplinary Medical Sciences, University of Szeged Szeged Hungary.

Anett Dunai (A)

Synthetic and Systems Biology Unit, Biological Research Centre, Eötvös Loránd Research Network (ELKH) Szeged Hungary.

Pramod K Jangir (PK)

Synthetic and Systems Biology Unit, Biological Research Centre, Eötvös Loránd Research Network (ELKH) Szeged Hungary.

Lejla Daruka (L)

Synthetic and Systems Biology Unit, Biological Research Centre, Eötvös Loránd Research Network (ELKH) Szeged Hungary.
Doctoral School of Biology, Faculty of Science and Informatics, University of Szeged Szeged Hungary.

Imre Földesi (I)

Department of Laboratory Medicine, University of Szeged Szeged Hungary.

Diána Kata (D)

Doctoral School of Biology, Faculty of Science and Informatics, University of Szeged Szeged Hungary.

Csaba Pál (C)

Synthetic and Systems Biology Unit, Biological Research Centre, Eötvös Loránd Research Network (ELKH) Szeged Hungary.

Tamás A Martinek (TA)

Department of Medical Chemistry, University of Szeged Dóm tér 8 Szeged HU-6720 Hungary martinek.tamas@med.u-szeged.hu.

Classifications MeSH