| Literature DB >> 28879611 |
Robbin Schnieders1, Christian Richter1, Sven Warhaut1, Vanessa de Jesus1, Sara Keyhani1, Elke Duchardt-Ferner2, Heiko Keller2, Jens Wöhnert2, Lars T Kuhn3, Alexander L Breeze3, Wolfgang Bermel4, Harald Schwalbe5, Boris Fürtig6.
Abstract
Recently, 15N-detected multidimensional NMR experiments have been introduced for the investigation of proteins. Utilization of the slow transverse relaxation of nitrogen nuclei in a 15N-TROSY experiment allowed recording of high quality spectra for high molecular weight proteins, even in the absence of deuteration. Here, we demonstrate the applicability of three 15N-detected H-N correlation experiments (TROSY, BEST-TROSY and HSQC) to RNA. With the newly established 15N-detected BEST-TROSY experiment, which proves to be the most sensitive 15N-detected H-N correlation experiment, spectra for five RNA molecules ranging in size from 5 to 100 kDa were recorded. These spectra yielded high resolution in the 15N-dimension even for larger RNAs since the increase in line width with molecular weight is more pronounced in the 1H- than in the 15N-dimension. Further, we could experimentally validate the difference in relaxation behavior of imino groups in AU and GC base pairs. Additionally, we showed that 15N-detected experiments theoretically should benefit from sensitivity and resolution advantages at higher static fields but that the latter is obscured by exchange dynamics within the RNAs.Keywords: 15N direct detection; BEST-TROSY; Exchange; Field dependence; Line width analysis; RNA
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Year: 2017 PMID: 28879611 DOI: 10.1007/s10858-017-0132-7
Source DB: PubMed Journal: J Biomol NMR ISSN: 0925-2738 Impact factor: 2.835