| Literature DB >> 27693721 |
Robb Welty1, Kathleen B Hall2.
Abstract
The tertiary structure of the GTPase center (GAC) of 23S ribosomal RNA (rRNA) as seen in cocrystals is extremely compact. It is stabilized by long-range hydrogen bonds and nucleobase stacking and by a triloop that forms within its three-way junction. Its folding pathway from secondary structure to tertiary structure has not been previously observed, but it was shown to require Mg2+ ions in equilibrium experiments. The fluorescent nucleotide 2-aminopurine was substituted at selected sites within the 60-nt GAC. Fluorescence intensity changes upon addition of MgCl2 were monitored over a time-course from 1ms to 100s as the RNA folds. The folding pathway is revealed here to be hierarchical through several intermediates. Observation of the nucleobases during folding provides a new perspective on the process and the pathway, revealing the dynamics of nucleobase conformational exchange during the folding transitions.Entities:
Keywords: 2-aminopurine fluorescence; GTPase center RNA; RNA folding kinetics; stopped-flow fluorescence
Mesh:
Substances:
Year: 2016 PMID: 27693721 PMCID: PMC5085838 DOI: 10.1016/j.jmb.2016.09.015
Source DB: PubMed Journal: J Mol Biol ISSN: 0022-2836 Impact factor: 5.469