| Literature DB >> 26661511 |
Elke Duchardt-Ferner1, Sina R Gottstein-Schmidtke1, Julia E Weigand2, Oliver Ohlenschläger3, Jan-Philip Wurm1, Christian Hammann4, Beatrix Suess2, Jens Wöhnert5.
Abstract
To ensure appropriate metabolic regulation, riboswitches must discriminate efficiently between their target ligands and chemically similar molecules that are also present in the cell. A remarkable example of efficient ligand discrimination is a synthetic neomycin-sensing riboswitch. Paromomycin, which differs from neomycin only by the substitution of a single amino group with a hydroxy group, also binds but does not flip the riboswitch. Interestingly, the solution structures of the two riboswitch-ligand complexes are virtually identical. In this work, we demonstrate that the local loss of key intermolecular interactions at the substitution site is translated through a defined network of intramolecular interactions into global changes in RNA conformational dynamics. The remarkable specificity of this riboswitch is thus based on structural dynamics rather than static structural differences. In this respect, the neomycin riboswitch is a model for many of its natural counterparts.Entities:
Keywords: RNA structures; aminoglycoside; ligand specificity; riboswitches; structural biology
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Year: 2015 PMID: 26661511 DOI: 10.1002/anie.201507365
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336