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.
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CITATION STYLE
Nakagawa, O., Ono, S., Tsujimoto, A., Li, Z., & Sasaki, S. (2006). Fluorescence detection of 8-oxoguanosine by G-clamp derivatives. Nucleic Acids Symposium Series (2004), (50), 21–22. https://doi.org/10.1093/nass/nrl011
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