Suppression of SARS‐CoV‐2 Replication with Stabilized and Click‐Chemistry Modified siRNAs. Issue 38 (12th August 2022)

• Record Type: Journal Article
• Authors: Traube, Franziska R.; Stern, Marcel; Tölke, Annika J.; Rudelius, Martina; Mejías‐Pérez, Ernesto; Raddaoui, Nada; Kümmerer, Beate M.; Douat, Céline; Streshnev, Filipp; Albanese, Manuel; Wratil, Paul R.; Gärtner, Yasmin V.; Nainytė, Milda; Giorgio, Grazia; Michalakis, Stylianos; Schneider, Sabine; Streeck, Hendrik; Müller, Markus; Keppler, Oliver T.; Carell, Thomas
• Is Part Of: Angewandte Chemie international edition. Volume 61:Issue 38(2022)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2022-08-12
• Subjects: Corona pandemic -- SARS-CoV-2 -- antiviral compounds -- siRNA -- peptide RNA conjugates; Chemistry -- Periodicals; 540
• DOI: 10.1002/anie.202204556
• Languages: English
• ISSNs: 1433-7851

Abstract

Abstract: The emergence of more transmissible or aggressive variants of SARS‐CoV‐2 requires the development of antiviral medication that is quickly adjustable to evolving viral escape mutations. Here we report the synthesis of chemically stabilized small interfering RNA (siRNA) against SARS‐CoV‐2. The siRNA can be further modified with receptor ligands such as peptides using Cu I ‐catalysed click‐chemistry. We demonstrate that optimized siRNAs can reduce viral loads and virus‐induced cytotoxicity by up to five orders of magnitude in cell lines challenged with SARS‐CoV‐2. Furthermore, we show that an ACE2‐binding peptide‐conjugated siRNA is able to reduce virus replication and virus‐induced apoptosis in 3D mucociliary lung microtissues. The adjustment of the siRNA sequence allows a rapid adaptation of their antiviral activity against different variants of concern. The ability to conjugate the siRNA via click‐chemistry to receptor ligands facilitates the construction of targeted siRNAs for a flexible antiviral defence strategy. Abstract : siRNAs protect cells from SARS‐CoV‐2 and can be quickly adjusted to variants of concern. An alkyne moiety was integrated at the 3′ end of the siRNA to enable chemical modification of the siRNA via Cu I ‐catalysed click‐chemistry. Following this strategy, the siRNA can be conjugated to receptor ligands such as hACE2‐binding peptides, which allows target‐specific delivery.