RNA kink-turns as molecular elbows: hydration, cation binding, and large-scale dynamics
Language English Country United States Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
Grant support
GR067507
Wellcome Trust - United Kingdom
PubMed
16698544
DOI
10.1016/j.str.2006.02.012
PII: S0969-2126(06)00178-X
Knihovny.cz E-resources
- MeSH
- Cations chemistry MeSH
- Nucleic Acid Conformation * MeSH
- Crystallography, X-Ray MeSH
- RNA, Ribosomal chemistry MeSH
- Binding Sites MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Cations MeSH
- RNA, Ribosomal MeSH
The presence of Kink-turns (Kt) at key functional sites in the ribosome (e.g., A-site finger and L7/L12 stalk) suggests that some Kink-turns can confer flexibility on RNA protuberances that regulate the traversal of tRNAs during translocation. Explicit solvent molecular dynamics demonstrates that Kink-turns can act as flexible molecular elbows. Kink-turns are associated with a unique network of long-residency static and dynamical hydration sites that is intimately involved in modulating their conformational dynamics. An implicit solvent conformational search confirms the flexibility of Kink-turns around their X-ray geometries and identifies a second low-energy region with open structures that could correspond to Kink-turn geometries seen in solution experiments. An extended simulation of Kt-42 with the factor binding site (helices 43 and 44) shows that the local Kt-42 elbow-like motion fully propagates beyond the Kink-turn, and that there is no other comparably flexible site in this rRNA region. Kink-turns could mediate large-scale adjustments of distant RNA segments.
References provided by Crossref.org
RNA kink-turns are highly anisotropic with respect to lateral displacement of the flanking stems
RNA Structural Dynamics As Captured by Molecular Simulations: A Comprehensive Overview
Molecular mechanism of preQ1 riboswitch action: a molecular dynamics study
Theoretical studies of RNA catalysis: hybrid QM/MM methods and their comparison with MD and QM
Conformations of flanking bases in HIV-1 RNA DIS kissing complexes studied by molecular dynamics