Abstract The essential role played by local and collective motions in RNA function has led to a growing interest in the characterization of RNA dynamics. Recent investigations have revealed that even relatively simple RNAs experience complex motions over multiple time scales covering the entire msā??ps motional range. In this work, we use deuterium solid-state NMR to systematically investigate motions in HIV-1 TAR RNA as a function of hydration. We probe dynamics at three uridine residues in different structural environments ranging from helical to completely unrestrained. We observe distinct and substantial changes in 2H solid-state relaxation times and lineshapes at each site as hydration levels increase. By comparing solid-state and solution state 13C relaxation measurements, we establish that nsā??Ī¼s motions that may be indicative of collective dynamics suddenly arise in the RNA as hydration reaches a critical point coincident with the onset of bulk hydration. Beyond that point, we observe smaller changes in relaxation rates and lineshapes in these highly hydrated solid samples, compared to the dramatic activation of motion occurring at moderate hydration.
Content Type Journal Article
Pages 133-142
DOI 10.1007/s10858-009-9355-6
Authors
Greg L. Olsen, University of Washington Department of Chemistry Box 351700 Seattle WA 98195 USA
Michael F. Bardaro, University of Washington Department of Chemistry Box 351700 Seattle WA 98195 USA
Dorothy C. Echodu, University of Washington Department of Chemistry Box 351700 Seattle WA 98195 USA
Gary P. Drobny, University of Washington Department of Chemistry Box 351700 Seattle WA 98195 USA
Gabriele Varani, University of Washington Department of Chemistry Box 351700 Seattle WA 98195 USA
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