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      Nucleic acid 3'-end recognition by the Argonaute2 PAZ domain.

      Nature Structural & Molecular Biology
      Argonaute Proteins, Binding Sites, Drosophila Proteins, chemistry, metabolism, Nuclear Magnetic Resonance, Biomolecular, Nucleic Acids, Protein Binding, Protein Conformation, RNA, Small Interfering, RNA-Induced Silencing Complex, Solutions

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          Abstract

          We describe the solution structures of the Argonaute2 PAZ domain bound to RNA and DNA oligonucleotides. The structures reveal a unique mode of single-stranded nucleic acid binding in which the two 3'-terminal nucleotides are buried in a hydrophobic cleft. We propose that the PAZ domain contributes to the specific recognition of siRNAs by providing a binding pocket for their characteristic two-nucleotide 3' overhangs.

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