Publication | Open Access
Structure/cleavage-based insights into helical perturbations at bulge sites within T. thermophilus Argonaute silencing complexes
30
Citations
24
References
2017
Year
Protein AssemblyBiomolecular Structure PredictionStructural BioinformaticsMolecular BiologyHelical PerturbationsProtein FoldingProtein X-ray CrystallographyBulge SitesBulge SiteMulti-protein AssemblyBiophysicsBulge BaseBiochemistryDna ReplicationConformational StudyStructural BiologyArgonaute Silencing ComplexesNatural SciencesProtein EngineeringSystematic Structural StudyMedicine
We have undertaken a systematic structural study of Thermus thermophilus Argonaute (TtAgo) ternary complexes containing single-base bulges positioned either within the seed segment of the guide or target strands and at the cleavage site. Our studies establish that single-base bulges 7T8, 5A6 and 4A5 on the guide strand are stacked-into the duplex, with conformational changes localized to the bulge site, thereby having minimal impact on the cleavage site. By contrast, single-base bulges 6'U7' and 6'A7' on the target strand are looped-out of the duplex, with the resulting conformational transitions shifting the cleavable phosphate by one step. We observe a stable alignment for the looped-out 6'N7' bulge base, which stacks on the unpaired first base of the guide strand, with the looped-out alignment facilitated by weakened Watson-Crick and reversed non-canonical flanking pairs. These structural studies are complemented by cleavage assays that independently monitor the impact of bulges on TtAgo-mediated cleavage reaction.
| Year | Citations | |
|---|---|---|
Page 1
Page 1