Rapid and specific purification of Argonaute-small RNA complexes from crude cell lysates

45Citations
Citations of this article
150Readers
Mendeley users who have this article in their library.

Abstract

Small interfering RNAs (siRNAs) direct Argonaute proteins, the core components of the RNA-induced silencing complex (RISC), to cleave complementary target RNAs. Here, we describe a method to purify active RISC containing a single, unique small RNA guide sequence. We begin by capturing RISC using a complementary 2'-O-methyl oligonucleotide tethered to beads. Unlike other methods that capture RISC but do not allow its recovery, our strategy purifies active, soluble RISC in good yield. The method takes advantage of the finding that RISC partially paired to a target through its siRNA guide dissociates more than 300 times faster than a fully paired siRNA in RISC. We use this strategy to purify fly Ago1- and Ago2-RISC, as well as mouse AGO2-RISC. The method can discriminate among RISCs programmed with different guide strands, making it possible to deplete and recover specific RISC populations. Endogenous microRNA:Argonaute complexes can also be purified from cell lysates. Our method scales readily and takes less than a day to complete. Copyright © 2013 RNA Society.

Author supplied keywords

Cite

CITATION STYLE

APA

Flores-Jasso, C. F., Salomon, W. E., & Zamore, P. D. (2013). Rapid and specific purification of Argonaute-small RNA complexes from crude cell lysates. RNA, 19(2), 271–279. https://doi.org/10.1261/rna.036921.112

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free