Membrane‐Associated Nucleobase‐Functionalized β‐Peptides (β‐PNAs) Affecting Membrane Support and Lipid Composition

Abstract: Protein‐membrane interactions are essential to maintain membrane integrity and control membrane morphology and composition. Cytoskeletal proteins in particular are known to interact to a high degree with lipid bilayers and to line the cytoplasmic side of the plasma membrane with an extensive network structure. In order to gain a better mechanistical understanding of the protein–membrane interplay and possible membrane signaling, we started to develop a model system based on β‐peptide nucleic acids (β‐PNAs). These β‐peptides are known to form stable hydrogen‐bonded aggregates due to their helical secondary structure, which serve to pre‐organize the attached nucleobases. After optimization of the β‐PNA solid‐phase peptide synthesis and validation of helix formation, the ability of the novel β‐PNAs to dimerize and interact with lipid bilayers was investigated by both fluorescence and circular dichroism spectroscopy. It was shown that duplex formation occurs rapidly and with high specificity and could also be detected on the surfaces of the lipid bilayers. Hereby, the potential of a β‐PNA‐based peptide system to mimic membrane‐associated protein networks could be demonstrated.

Location
Deutsche Nationalbibliothek Frankfurt am Main
Extent
Online-Ressource
Language
Englisch

Bibliographic citation
Membrane‐Associated Nucleobase‐Functionalized β‐Peptides (β‐PNAs) Affecting Membrane Support and Lipid Composition ; volume:21 ; number:18 ; year:2020 ; pages:2599-2603 ; extent:5
ChemBioChem ; 21, Heft 18 (2020), 2599-2603 (gesamt 5)

Creator
Höger, Geralin A.
Wiegand, Markus
Worbs, Brigitte
Diederichsen, Ulf

DOI
10.1002/cbic.202000172
URN
urn:nbn:de:101:1-2022061805263223656534
Rights
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Last update
15.08.2025, 7:20 AM CEST

Data provider

This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.

Associated

Other Objects (12)