13C-NMR of the deoxyribose sugars in four DNA oligonucleotide duplexes: assignment and structural features.
13C-NMR of the deoxyribose sugars in four DNA oligonucleotide duplexes: assignment and structural features.
复制标题
四种 DNA 寡核苷酸双链体中脱氧核糖的 13C-NMR:分配和结构特征。
DOI:
10.1021/bi00175a011
复制
发表时间:
1994
期刊:
影响因子:
2.9
通讯作者:
Borer,PN
中科院分区:
文献类型:
--
作者:
LaPlante,SR;Zanatta,N;Hakkinen,A;Wang,AH;Borer,PN
November 24, 19939 abstract: Natural-abundance 13C-NMR spectra have been obtained for four self-complementary DNA oligonucleotides:[d (TAGCGCTA)] 2,[d (GGTATACC)] 2,[d (CG) 3] 2, and [d (TCGCG)] 2; this paperfocuses on the deoxyribose resonances. Assignments were made by a combination of the two-dimensional proton-detected heteronuclear correlation experiment and comparison of ID spectra, accounting for 31P coupling, base composition, and similarities in chemical shift versus temperature profiles (5 vs T). Large shielding and deshielding of the sugar resonances(between 2.0 and-1.9 ppm) are observed upon thermal dissociation of the duplex. The shapes of the 8 vs T profiles correlate strongly with the purine/pyrimidine nature of the base attached at Cl'in these duplexes that have a substantial fraction of residues within alternating purine-pyrimidine sequences. The correlation is primarily associated with changes in the equilibrium distribution of furanose pseudorotational states that mayarise inpart from the relief of interstrand purine-purine steric clashes.