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The binding of substituted cis ‐Pt(II)‐diammines to duplex DNA
Author(s) -
McCarthy Sharon L.,
Hinde Robert J.,
Miller Kenneth J.,
Anderson Janet S.,
Basch Harold,
Krauss Morris
Publication year - 1990
Publication title -
biopolymers
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.556
H-Index - 125
eISSN - 1097-0282
pISSN - 0006-3525
DOI - 10.1002/bip.360290412
Subject(s) - chemistry , substituent , guanine , dna , stereochemistry , pentamer , van der waals force , ligand (biochemistry) , duplex (building) , crystallography , molecular mechanics , molecular dynamics , computational chemistry , molecule , nucleotide , receptor , biochemistry , organic chemistry , gene
The results of a study of the binding to DNA of substituted cis ‐Pt(II) diammines, ( cis ‐DP) are presented. Computer modeling of a series of cis ‐Pt(NH 2 R) 2 +2 —where R = H, CH 3 , cyclopropyl, cyclobutyl, and cyclopentyl—to N7(G) atoms of two adjacent intrastrand guanine bases in a square planar complex in a pentamer duplex of DNA were performed. The stability of the complexes is studied by calculating the relative conformational energy of the cis ‐DP–DNA complexes with molecular mechanics ( MM ) and the intrinsic binding energy, which is the relative binding energy for ligand replacement in the presence of the substituents R with quantum mechanics. In the model, the receptor site geometry and the conformation of the DNA is changed little in the accommodation of the series of monosubstituted diammines. These diammines bind to one family of DNA conformations, denoted as IC in a previous study, and this suggests that a common conformational feature in the DNA may exist to explain the smooth trend in activity. The slight increase in van der Waals energy resulting from an increasing number of atoms in the substituents is countered by a larger decrease in the ligand replacement energy as the substituent increases in size. This overall decrease in relative energy is consistent with the slight decrease in activity as the substituent size increases.