Abstract
8-Oxoguanosine, which is derived by the oxidation of guanosine (dG), is known to induce transversion mutations (G:C-->T:A) in DNA. The compounds with small molecular weight for recognizing 8-oxoG were designed on the basis of the structure of the G-clamp, which is reported to have selective affinity toward guanosine. The G-clamp derivatives with the additional binding units toward 8-oxoG were effectively synthesized and named "8-oxoG-clamps". Binding properties were measured by fluorescence quenching of 8-oxoG-clamps. Among the synthesized derivatives, 8-oxoG-clamp with N-benzyloxycarbonyl (Cbz) unit completely discriminated 8-oxoG from other nucleosides by fluorescence quenching.
Original language | English |
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Pages (from-to) | 21-22 |
Number of pages | 2 |
Journal | Nucleic acids symposium series (2004) |
Issue number | 50 |
DOIs | |
Publication status | Published - 2006 |
All Science Journal Classification (ASJC) codes
- Medicine(all)