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| Content Provider | Royal Society of Chemistry (RSC) |
|---|---|
| Author | Wang, Peng Zhang, Hui-Juan Wang, Xue-Fei Ai, Xi-Cheng Zhang, Jian-Ping |
| Copyright Year | 2008 |
| Abstract | We have performed systematic spectroscopic titrations to characterize the binding reaction of cationic meso-tetrakis(4-(N-methylpyridiumyl))porphyrin (TMPyP4) with the G-quadruplex (G4) of human telomeric single-strand oligonucleotide d[TAGGG(TTAGGG)3T] (S24), for which special effort was made to examine the TMPyP4-G4 binding stoichiometry, the binding modes, and the conformational conversion of the G4 structure under different potassium ion (K+) concentration. It is found that, in the presence of 0, 10 mM, and 100 mM K+, TMPyP4 forms a complex with the anti-parallel G4 in a TMPyP4-to-G4 molar ratio of 5, 5 and 3, respectively, and the increase of K+ concentration would reduce the binding affinity of TMPyP4 to G4. For the TMPyP4–G4 complex, the end-stacking mode and groove binding mode were presumed mainly by the results of time-resolved fluorescence spectroscopy in the three cases. Most importantly, it is found that TMPyP4 can directly induce the formation of the anti-parallel G4 structure from the single-strand oligonucleotide S24 in the absence of K+, and that it can preferentially induce the conformational conversion of the G4 structure from the hybrid-type to the anti-parallel one in the presence of K+. |
| Starting Page | 948 |
| Ending Page | 955 |
| Page Count | 8 |
| File Format | HTM / HTML PDF |
| ISSN | 1474905X |
| Volume Number | 7 |
| Issue Number | 8 |
| Journal | Photochemical & Photobiological Sciences |
| DOI | 10.1039/b809322a |
| Language | English |
| Publisher | Royal Society of Chemistry |
| Access Restriction | Open |
| Subject Keyword | Special Effort Stoichiometry Spectroscopy Porphyrin G-quadruplex Fluorescence Ion Oligonucleotide S24 (ZVV) Potassium Molar concentration Power Mac G4 |
| Content Type | Text |
| Resource Type | Article |
| Subject | Physical and Theoretical Chemistry |
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