Journal article

NMR study of the p-DNA duplex [(4'->2')-3'-desoxyribopyranosyl-(m5CGDDTTm5CG)2] and comparison with its p-RNA analogue

The detn. of the soln. 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 analog 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 qual. conformational anal. than p-RNA. [on SciFinder (R)]


    • LCAN-ARTICLE-2001-001

    Record created on 2006-02-27, modified on 2016-08-08


  • There is no available fulltext. Please contact the lab or the authors.

Related material