Rinnenthal Jörg, Richter Christian, Nozinovic Senada, Fürtig Boris, Lopez Jakob J, Glaubitz Clemens, Schwalbe Harald
Institute for Organic Chemistry and Chemical Biology, Center for Biomolecular Magnetic Resonance, Johann Wolfgang Goethe-University, Max-von-Laue-Strasse 7, Frankfurt/Main, Germany.
J Biomol NMR. 2009 Sep;45(1-2):143-55. doi: 10.1007/s10858-009-9343-x. Epub 2009 Jul 28.
We have analyzed the relaxation properties of all (31)P nuclei in an RNA cUUCGg tetraloop model hairpin at proton magnetic field strengths of 300, 600 and 900 MHz in solution. Significant H, P dipolar contributions to R (1) and R (2) relaxation are observed in a protonated RNA sample at 600 MHz. These contributions can be suppressed using a perdeuterated RNA sample. In order to interpret the (31)P relaxation data (R (1), R (2)), we measured the (31)P chemical shift anisotropy (CSA) by solid-state NMR spectroscopy under various salt and hydration conditions. A value of 178.5 ppm for the (31)P CSA in the static state (S (2) = 1) could be determined. In order to obtain information about fast time scale dynamics we performed a modelfree analysis on the basis of our relaxation data. The results show that subnanosecond dynamics detected around the phosphodiester backbone are more pronounced than the dynamics detected for the ribofuranosyl and nucleobase moieties of the individual nucleotides (Duchardt and Schwalbe, J Biomol NMR 32:295-308, 2005; Ferner et al., Nucleic Acids Res 36:1928-1940, 2008). Furthermore, the dynamics of the individual phosphate groups seem to be correlated to the 5' neighbouring nucleobases.
我们在溶液中,于300、600和900兆赫的质子磁场强度下,分析了RNA cUUCGg四环模型发夹中所有磷(³¹P)核的弛豫特性。在600兆赫的质子化RNA样品中,观察到氢-磷偶极对R(1)和R(2)弛豫有显著贡献。使用全氘代RNA样品可抑制这些贡献。为了解释磷(³¹P)弛豫数据(R(1)、R(2)),我们在各种盐和水合条件下,通过固态核磁共振光谱法测量了磷(³¹P)化学位移各向异性(CSA)。可确定静态(S(2)=1)下磷(³¹P)CSA的值为178.5 ppm。为了获得关于快速时间尺度动力学的信息,我们基于弛豫数据进行了无模型分析。结果表明,在磷酸二酯主链周围检测到的亚纳秒动力学比在单个核苷酸的呋喃核糖基和核碱基部分检测到的动力学更明显(Duchardt和Schwalbe,《生物分子核磁共振杂志》32:295 - 308,2005;Ferner等人,《核酸研究》36:1928 - 1940,2008)。此外,各个磷酸基团的动力学似乎与5'相邻核碱基相关。