2E4I
Human Telomeric DNA mixed-parallel/antiparallel quadruplex under Physiological Ionic Conditions Stabilized by Proper Incorporation of 8-Bromoguanosines
2E4I の概要
| エントリーDOI | 10.2210/pdb2e4i/pdb |
| 分子名称 | DNA (5'-D(*DAP*(BGM)P*DGP*DGP*DTP*DTP*DAP*(BGM)P*DGP*DGP*DTP*DTP*DAP*(BGM)P*(BGM)P*DGP*DTP*DTP*DAP*(BGM)P*DGP*DG)-3') (1 entity in total) |
| 機能のキーワード | telomere, quadruplex, mixed-parallel/antiparallel, dna |
| タンパク質・核酸の鎖数 | 1 |
| 化学式量合計 | 7377.98 |
| 構造登録者 | Matsugami, A.,Xu, Y.,Noguchi, Y.,Sugiyama, H.,Katahira, M. (登録日: 2006-12-11, 公開日: 2007-12-11, 最終更新日: 2024-05-29) |
| 主引用文献 | Matsugami, A.,Xu, Y.,Noguchi, Y.,Sugiyama, H.,Katahira, M. Structure of a human telomeric DNA sequence stabilized by 8-bromoguanosine substitutions, as determined by NMR in a K+ solution Febs J., 274:3545-3556, 2007 Cited by PubMed Abstract: The structure of human telomeric DNA is controversial; it depends upon the sequence contexts and the methodologies used to determine it. The solution structure in the presence of K(+) is particularly interesting, but the structure is yet to be elucidated, due to possible conformational heterogeneity. Here, a unique strategy is applied to stabilize one such structure in a K(+) solution by substituting guanosines with 8-bromoguanosines at proper positions. The resulting spectra are cleaner and led to determination of the structure at a high atomic resolution. This demonstrates that the application of 8-bromoguanosine is a powerful tool to overcome the difficulty of nucleic acid structure determination arising from conformational heterogeneity. The obtained structure is a mixed-parallel/antiparallel quadruplex. The structure of telomeric DNA was recently reported in another study, in which stabilization was brought about by mutation and resultant additional interactions [Luu KN, Phan AT, Kuryavyi V, Lacroix L & Patel DJ (2006) Structure of the human telomere in K(+) solution: an intramolecular (3+1) G-quadruplex scaffold. J Am Chem Soc 128, 9963-9970]. The structure of the guanine tracts was similar between the two. However, a difference was seen for loops connecting guanine tracts, which may play a role in the higher order arrangement of telomeres. Our structure can be utilized to design a small molecule which stabilizes the quadruplex. This type of molecule is supposed to inhibit a telomerase and thus is expected to be a candidate anticancer drug. PubMed: 17561958DOI: 10.1111/j.1742-4658.2007.05881.x 主引用文献が同じPDBエントリー |
| 実験手法 | SOLUTION NMR |
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