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Interaction between double helix DNA fragments and a new topopyrone acting as human topoisomerase I poison
Authors:Leonardo Scaglioni  Stefania Mazzini  Rosanna Mondelli  Sabrina Dallavalle  Sonia Gattinoni  Stella Tinelli  Giovanni L Beretta  Franco Zunino  Enzio Ragg
Institution:1. Dipartimento di Scienze Molecolari Agroalimentari, Università di Milano, via Celoria 2, 20133 Milano, Italy;2. Department of Experimental Oncology and Laboratories, Fondazione IRCCS Istituto Nazionale dei Tumori, via Venezian 1, 20133 Milano, Italy
Abstract:A water soluble derivative (2) of topopyrones was selected for NMR studies directed to elucidate the mode of binding with specific oligonucleotides. Topopyrone 2 can intercalate into the CG base pairs, but the residence time into the double helix is very short and a fast chemical exchange averaging occurs at room temperature between the free and bound species. The equilibria involved become slow below room temperature, thus allowing to measure a mean lifetime of the complex of ca. 7 ms at 15 °C. Structural models of the complex with d(CGTACG)2 were developed on the basis of DOSY, 2D NOESY and 31P NMR experiments. Topopyrone 2 presents a strong tendency to self-associate. In the presence of oligonucleotide a certain number of ligand molecules are found to externally stack to the double-helix, in addition to a small fraction of the same ligand intercalated. The external binding to the ionic surface of the phosphoribose chains may thus represents the first step of the intercalation process.
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