Nucleic Acids Research, 1982, Vol. 10, No. 11 3573-3588
© 1982
CHEMISTRY |
Binding of [(dien)PtCl]Cl to poly(dG-dC).poly(dG-dC) facilitates the B
Z conformational transition
*Department of Chemistry, Columbia University New York, NY 10027
The Cancer Center/Institute of Cancer Research, Columbia University College of Physicians and Surgeons New York, NY 10032, USA
Received February 10, 1982. Revised May 4, 1982. Accepted May 13, 1982.
Chlorodiethylenetriamineplatinum(II) chloride, [(dien)ptCl]Cl bound to 
10% of the nucleotide bases of poly(dG-dC)· poly(dG-dC) reduces the amount of ethanol necessary to bring about the B
Z conformational transition in proportion to the amount of platinum complex bound as monitored by CD spectroscopy. The transition may be effected by 25% ethanol with 9.3% of the bases modified and by 36% ethanol with 5.4% of the bases modified. With an unmodified polymer an ethanol concentration of 55–60% is necessary to bring about the transition. The assignment of the Z conformation was supported by P NMR spectroscopy. This covalent modification of the DNA is reversed by treatment with cyanide ion after which the normal amount of ethanol is necessary to achieve the transition. The platinum complex shows no enhanced binding to DNA in the Z versus the B conformation. Between 20 and 33% (saturation binding) modification, [(dien)PtCl]Cl binds cooperatively to the heterocopolymer as judged by CD spectroscopy. At. this high level of modification it is no longer possible to induce the 1 DNA structure with ethanol. When [(dien)PtCl]Cl is bound to preformed (with ethanol) Z DNA at saturating levels the CD spectrum is altered but reverts to the spectrum of highly modified DNA upon removal of ethanol. The antitumor drug cis-diamminedichloroplatinum(II), cis-DDP, binds to poly(dG-dC)·poly(dG-dC) and alters the CD spectrum. It does not facilitate the BZ conformational change, however, and actually prevents it from happening even at very high ethanol concentrations.
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