Simorre J P, Zimmermann G R, Mueller L, Pardi A
Department of Chemistry and Biochemistry, University of Colorado at Boulder 80309-0215, USA.
J Biomol NMR. 1996 Mar;7(2):153-6. doi: 10.1007/BF00203825.
A triple resonance HNC-TOCSY-CH experiment is described for correlating the guanosine imino proton and H8 resonances in 13C-/15N-labeled RNAs. Sequential assignment of the exchangeable imino protons in Watson-Crick base pairs is generally made independently of the assignment of the nonexchangeable base protons. This H(NC)-TOCSY-(C)H experiment makes it possible to unambiguously link the assignment of the guanosine H8 resonances with sequential assignment of the guanosine imino proton resonances. 2D H(NC)-TOCSY-(C)H spectra are presented for two isotopically labeled RNAs, a 30-nucleotide lead-dependent ribozyme known as the leadzyme, and a 48-nucleotide hammerhead ribozyme-RNA substrate complex. The results obtained on these two RNAs demonstrate that this HNC-TOCSY-CH experiment is an important tool for resonance assignment of isotopically labeled RNAs.
本文描述了一种用于关联13C-/15N标记的RNA中鸟苷亚氨基质子和H8共振的三重共振HNC-TOCSY-CH实验。沃森-克里克碱基对中可交换亚氨基质子的顺序归属通常独立于不可交换碱基质子的归属。这种H(NC)-TOCSY-(C)H实验使得明确将鸟苷H8共振的归属与鸟苷亚氨基质子共振的顺序归属联系起来成为可能。给出了两种同位素标记RNA的二维H(NC)-TOCSY-(C)H谱,一种是30个核苷酸的铅依赖核酶(称为铅酶),另一种是48个核苷酸的锤头状核酶-RNA底物复合物。在这两种RNA上获得的结果表明,这种HNC-TOCSY-CH实验是同位素标记RNA共振归属的重要工具。