Environment‐Responsive Peptide Dimers Bind and Stabilize Double‐Stranded RNA

Abstract: Double‐stranded RNAs (dsRNA) possess immense potential for biomedical applications. However, their therapeutic utility is limited by low stability and poor cellular uptake. Different strategies have been explored to enhance the stability of dsRNA, including the incorporation of modified nucleotides, and the use of diverse carrier systems. Nevertheless, these have not resulted in a broadly applicable approach thereby preventing the wide‐spread application of dsRNA for therapeutic purposes. Herein, we report the design of dimeric stapled peptides based on the RNA‐binding protein TAV2b. These dimers are obtained via disulfide formation and mimic the natural TAV2b assembly. They bind and stabilize dsRNA in the presence of serum, protecting it from degradation. In addition, peptide binding also promotes cellular uptake of dsRNA. Importantly, peptide dimers monomerize under reducing conditions which results in a loss of RNA binding. These findings highlight the potential of peptide‐based RNA binders for the stabilization and protection of dsRNA, representing an appealing strategy towards the environment‐triggered release of RNA. This can broaden the applicability of dsRNA, such as short interfering RNAs (siRNA), for therapeutic applications.

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

Bibliographic citation
Environment‐Responsive Peptide Dimers Bind and Stabilize Double‐Stranded RNA ; day:31 ; month:08 ; year:2023 ; extent:7
Angewandte Chemie / International edition. International edition ; (31.08.2023) (gesamt 7)

Creator
McLoughlin, Niall M.
Albers, Marvin A.
Collado Camps, Estel
Paulus, Jannik
Ran, Youri A.
Neubacher, Saskia
Hennig, Sven
Brock, Roland
Großmann, Tom N.

DOI
10.1002/anie.202308028
URN
urn:nbn:de:101:1-2023083115425683735638
Rights
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Last update
14.08.2025, 10:46 AM CEST

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