Details

Autor(en) / Beteiligte

• Rajeev, Kallanthottathil G.
• Nair, Jayaprakash K.
• Jayaraman, Muthusamy
• Charisse, Klaus
• Taneja, Nate
• O'Shea, Jonathan
• Willoughby, Jennifer L. S.
• Yucius, Kristina
• Nguyen, Tuyen
• Shulga-Morskaya, Svetlana
• Milstein, Stuart
• Liebow, Abigail
• Querbes, William
• Borodovsky, Anna
• Fitzgerald, Kevin
• Maier, Martin A.
• Manoharan, Muthiah

Titel

Hepatocyte-Specific Delivery of siRNAs Conjugated to Novel Non-nucleosidic Trivalent N-Acetylgalactosamine Elicits Robust Gene Silencing in Vivo

Ist Teil von

• Chembiochem : a European journal of chemical biology, 2015-04, Vol.16 (6), p.903-908

Ort / Verlag

Weinheim: WILEY-VCH Verlag

Erscheinungsjahr

2015

Quelle

Wiley Online Library - AutoHoldings Journals

Beschreibungen/Notizen

• We recently demonstrated that siRNAs conjugated to triantennary N‐acetylgalactosamine (GalNAc) induce robust RNAi‐mediated gene silencing in the liver, owing to uptake mediated by the asialoglycoprotein receptor (ASGPR). Novel monovalent GalNAc units, based on a non‐nucleosidic linker, were developed to yield simplified trivalent GalNAc‐conjugated oligonucleotides under solid‐phase synthesis conditions. Synthesis of oligonucleotide conjugates using monovalent GalNAc building blocks required fewer synthetic steps compared to the previously optimized triantennary GalNAc construct. The redesigned trivalent GalNAc ligand maintained optimal valency, spatial orientation, and distance between the sugar moieties for proper recognition by ASGPR. siRNA conjugates were synthesized by sequential covalent attachment of the trivalent GalNAc to the 3′‐end of the sense strand and resulted in a conjugate with in vitro and in vivo potency similar to that of the parent trivalent GalNAc conjugate design. Sugar goes straight to the liver: An siRNA conjugate bearing three N‐acetylgalactosamine moieties, each sequentially attached by a non‐nucleosidic linker, was recognized by the asialoglycoprotein receptor with high affinity. The resulting liver‐specific delivery of the conjugate for robust RNAi‐mediated gene silencing in vivo shows potential for delivery of oligonucleotide therapeutics into hepatocytes.