NMR (13)C-relaxation study of base and sugar dynamics in GCAA RNA hairpin tetraloop
Jazyk angličtina Země Anglie, Velká Británie Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
17937486
DOI
10.1080/07391102.2007.10507173
PII: d=3028&c=4243&p=16223&do=detail
Knihovny.cz E-zdroje
- MeSH
- adenin chemie MeSH
- biologické modely * MeSH
- cytosin chemie MeSH
- konformace nukleové kyseliny MeSH
- magnetická rezonanční spektroskopie MeSH
- molekulární sekvence - údaje MeSH
- párování bází MeSH
- puriny chemie MeSH
- RNA chemie MeSH
- sacharidy chemie MeSH
- sekvence nukleotidů MeSH
- vodíková vazba MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- adenin MeSH
- cytosin MeSH
- puriny MeSH
- RNA MeSH
- sacharidy MeSH
Intramolecular dynamics of a 14-mer RNA hairpin including GCAA tetraloop was investigated by (13)C NMR relaxation. R(1) and R(1rho) relaxation rates were measured for all protonated base carbons as well as for C1' carbons of ribose sugars at several magnetic field strengths. The data has been interpreted in the framework of modelfree analysis [G. Lipari and A. Szabo. J Am Chem Soc 104, 4546-4559 (1982); G. Lipari and A. Szabo. J Am Chem Soc 104, 4559-4570 (1982)] characterizing the internal dynamics of the molecule by order parameters and correlation times for fast motions on picosecond to nanosecond time scale and by contributions of the chemical exchange. The fast dynamics reveals a rather rigid stem and a significantly more flexible loop. The cytosine and the last adenine bases in the loop as well as all the loop sugars exhibit a significant contribution of conformational equilibrium on microsecond to millisecond time scale. The high R(1rho) values detected on both base and sugar moieties of the loop indicate coordinated motions in this region. A semiquantitative analysis of the conformational equilibrium suggests the exchange rates on the order of 10(4) s(-1). The results are in general agreement with dynamics studies of GAAA loops by NMR relaxation and fluorescent spectroscopy and support the data on the GCAA loop dynamics obtained by MD simulations.
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