Stability and proton transfer in DNA base pairs of AMD473–DNA adduct

Abstract

We investigate the energetics of four different adducts of cisplatin analogue cis-[PtCl2(NH3)(2-picoline)] (AMD473) with a duplex DNA using DFT/ONIOM methods to probe their stabilities. Further, we study the possibilities of proton transfer between DNA base pairs of the most stable drug–DNA adduct. The adduct b (2-picoline trans to 30-G and 2-methyl group directs to the DNA major groove) is found to be the most stable configuration among all the possible adducts. From the proton transfer analysis we found that the single proton transfer between N1 position of guanine (G) and N3 position of cytosine (C) of each GC pair gives a structure energetically as stable as the original one.