13C-NMR of ribosyl A-A-A, A-A-G, AND A-U-G Synthesis and Assignment Article

Stone, MP, Winkle, SA, McFarland, GD et al. (1985). 13C-NMR of ribosyl A-A-A, A-A-G, AND A-U-G Synthesis and Assignment . Biophysical Chemistry, 23(1-2), 129-138. 10.1016/0301-4622(85)80071-5

cited authors

  • Stone, MP; Winkle, SA; McFarland, GD; Yoo, MC; Borer, PN

abstract

  • The three RNA trinucleotides; ApApA, ApApG, and ApUpG, have been synthesized in sufficient quantity to obtain natural abundance 13C{1H}-NMR spectra at strand concentrations between 4 and 100 mM. Comparisons between 70°C spectra of the three trimers and their consistuent dimers ApA, ApG, ApU, and UpG allow secure assignments to be made for most of the resonances. This paper describes the syntheses and 13C assignments of the oligomers. © 1985.

authors

publication date

  • January 1, 1985

published in

Digital Object Identifier (DOI)

start page

  • 129

end page

  • 138

volume

  • 23

issue

  • 1-2