| Literature DB >> 27121751 |
Rubina Parmar1, Jennifer L S Willoughby1, Jingxuan Liu1, Donald J Foster1, Benjamin Brigham1, Christopher S Theile1, Klaus Charisse1, Akin Akinc1, Erin Guidry2, Yi Pei2, Walter Strapps2, Mark Cancilla2, Matthew G Stanton2, Kallanthottathil G Rajeev1, Laura Sepp-Lorenzino1, Muthiah Manoharan1, Rachel Meyers1, Martin A Maier1, Vasant Jadhav3.
Abstract
Small interfering RNA (siRNA)-mediated silencing requires siRNA loading into the RNA-induced silencing complex (RISC). Presence of 5'-phosphate (5'-P) is reported to be critical for efficient RISC loading of the antisense strand (AS) by anchoring it to the mid-domain of the Argonaute2 (Ago2) protein. Phosphorylation of exogenous duplex siRNAs is thought to be accomplished by cytosolic Clp1 kinase. However, although extensive chemical modifications are essential for siRNA-GalNAc conjugate activity, they can significantly impair Clp1 kinase activity. Here, we further elucidated the effect of 5'-P on the activity of siRNA-GalNAc conjugates. Our results demonstrate that a subset of sequences benefit from the presence of exogenous 5'-P. For those that do, incorporation of 5'-(E)-vinylphosphonate (5'-VP), a metabolically stable phosphate mimic, results in up to 20-fold improved in vitro potency and up to a threefold benefit in in vivo activity by promoting Ago2 loading and enhancing metabolic stability.Entities:
Keywords: Clp1 kinase; RISC loading; oligonucleotides; phosphate mimic; siRNA
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Year: 2016 PMID: 27121751 DOI: 10.1002/cbic.201600130
Source DB: PubMed Journal: Chembiochem ISSN: 1439-4227 Impact factor: 3.164