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PMID: 8532537 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Synthesis and NMR of RNA with selective isotopic enrichment in the bases.

Nucleic acids research ·Vol. 23 ·No. 23 ·1995-12-11 ·Pages 4913-21

SantaLucia J, Shen LX, Cai Z, Lewis H, Tinoco I

Abstract

Efficient syntheses of pyrimidine and purine nucleosides and nucleotides with selective 13C enrichment in the base moieties are described. Uridine and cytidine are labeled at position C6 and adenosine and guanosine are labeled at position C8. The selectively labeled nucleosides were converted to nucleoside triphosphates and used with in vitro transcription to synthesize labeled RNA. Isotope-edited 12C and 13C sub-spectra of a omega 1-1/2-X-filtered NOESY experiment are demonstrated to be useful for making resonance assignments and for deriving structural information in large (> 20 nt) RNA molecules. The labeled RNAs also allow heteronuclear J-couplings and relaxation parameters to be measured without complications from 13C-13C J-couplings.

MeSH Terms
Adenine/chemical synthesis Cytidine/chemical synthesis Guanosine/chemical synthesis Magnetic Resonance Spectroscopy Purine Nucleosides/chemical synthesis Pyrimidine Nucleosides/chemical synthesis RNA/chemical synthesis,chemistry Uracil/chemical synthesis Uridine/chemical synthesis
Chemicals
Purine Nucleosides Pyrimidine Nucleosides Guanosine Uracil Cytidine RNA Adenine Uridine
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
SantaLucia J
Department of Chemistry, Lawrence Berkeley Laboratory, University of California, Berkeley 94720, USA.
Shen L X
Cai Z
Lewis H
Tinoco I
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Article Info
Journal
Nucleic acids research
Abbr.
Nucleic Acids Res
ISSN
0305-1048
Published
1995-12-11
Pages
4913-21
Language
English
Region
England
NLM ID
0411011
PMCID
PMC307483
Subset
IM
Grants
NIGMS NIH HHS · GM10840 · United States
NIGMS NIH HHS · GM14682 · United States
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