1AC3
SOLUTION STRUCTURE OF AN RNA-DNA HYBRID DUPLEX CONTAINING A 3'-THIOFORMACETAL LINKER AND AN RNA A-TRACT, NMR, 8 STRUCTURES
1AC3 の概要
| エントリーDOI | 10.2210/pdb1ac3/pdb |
| 分子名称 | ANTISENSE HYBRID DUPLEX, DNA (5'-D(*(TCP)P*TP*GP*CP*GP*C)-3') (2 entities in total) |
| 機能のキーワード | rna, dna, antisense oligonucleotides, thioformacetal backbone modification, hybrid duplex, dna-rna hybrid complex, dna-rna hybrid |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 7468.89 |
| 構造登録者 | |
| 主引用文献 | Cross, C.W.,Rice, J.S.,Gao, X. Solution structure of an RNA x DNA hybrid duplex containing a 3'-thioformacetal linker and an RNA A-tract. Biochemistry, 36:4096-4107, 1997 Cited by PubMed Abstract: Neutral and achiral backbone linkers are promising replacements for the phosphodiester linkages of antisense oligonucleotides that target mRNA sequences. Results are presented here for the solution structure elucidation by NMR of an RNA x DNA hybrid duplex, r(GCGCAAAACGCG) x d(CGCGTT-SCH2O-TTGCGC) (designated RIII), containing a 3'-thioformacetal (3'-TFMA) backbone substitution in the DNA strand. The 3'-thioformacetal linker can be accommodated in the hybrid duplex in a conformation that is drastically different from its form in a DNA x DNA duplex but close to that of the canonical A-form helix, reflecting the sequence requirement for hybridization. While the global features of RIII are similar to what are described in the literature, the 3'-TFMA modification drives sugar puckers of the adjacent residues to more C3'-endo-like conformations and causes distortions in related twist angles and helical rises. The helical conformation analyses of each of the two strands and the hybrid duplex enable a clear account of the conformational variability of both the DNA and RNA strands. The A-tract in the RNA strand features an overall straight helix and a more prominent bend at the 3'-end CG step. The structure of RIII provides a structural basis for the improved thermal stability of RIII compared to the corresponding DNA x DNA duplex and insights into the factors that are important concerns for the design of new, effective antisense oligonucleotides. PubMed: 9100003DOI: 10.1021/bi962382k 主引用文献が同じPDBエントリー |
| 実験手法 | SOLUTION NMR |
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