NMR Study of the p-DNA Duplex [(4→?2')-3'-Desoxyribopyranosyl-(ᵐ⁵CGDDTTᵐ⁵CG)₂] and Comparison with its p-RNA Analogue
DOI:
https://doi.org/10.2533/chimia.2001.852Keywords:
p-DNA, Duplex formation, NMR solution structure, Pentapyranosyl nucleic acids, p-RNAAbstract
The determination of the solution structure of small non-natural oligopeptides and oligonucleotides by NMR, which is one of the main research topics of our group, is illustrated on the example of an 8-mer p-DNA duplex. p-DNA, the 3'-desoxy analogue of p-RNA, forms an highly selective pairing system but its pairing strength is less than that of analogous p-RNA sequences. The NMR study reveals that the backbone of p-DNA corresponds more closely to the conformation predicted for pentapyranose nucleic acids by qualitative conformational analysis than p-RNA.Downloads
Published
2001-10-31
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Scientific Articles
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Copyright (c) 2001 Swiss Chemical Society
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
How to Cite
[1]
Chimia 2001, 55, 852, DOI: 10.2533/chimia.2001.852.