X-ray structure of the major adduct of the anticancer drug cisplatin with DNA: cis-[Pt(NH3)2(d(pGpG))].

Abstract

Crystals of the adduct of the anticancer drug cis-diamminedichloroplatinum(II), cis-DDP, with d(pGpG), its putative target on DNA in the cancer cell, have been obtained and used in an x-ray crystallographic study to elucidate the molecular structure to atomic resolution. Each of the four crystallographically independent cis-[Pt(NH3)2(d(pGpG))] molecules is comprised of a square-planar platinum atom bonded to two ammonia ligands and two N(7) atoms of guanosine nucleosides from the same chain. Base stacking of the two adjacent guanine rings is completely disrupted by coordination to the cis-(Pt(NH3)2)2+ unit. Comparison of the backbone and deoxyribose ring torsion angles with those found by previous (nuclear magnetic resonance spectroscopy) studies of this adduct in solution demonstrates that the solid state geometry is substantially the same as that in solution. The relevance of these results to the molecular mechanism of action of cis-DDP is discussed.

• Authors: S E Sherman, D Gibson, A H Wang, S J Lippard
• Journal: Science (New York, N.Y.) (Science) Vol. 230 Issue 4724 Pg. 412-7 (Oct 25 1985) ISSN: 0036-8075 [Print] United States
• PMID: 4048939 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)

Chemical References

• Deoxyguanine Nucleotides
• deoxydiguanosine diphosphosphate
• DNA
• Cisplatin

Topics

• Cisplatin (metabolism, pharmacology)
• DNA (metabolism)
• Deoxyguanine Nucleotides (metabolism)
• Humans
• Hydrogen Bonding
• Magnetic Resonance Spectroscopy
• Molecular Conformation
• X-Ray Diffraction