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Title: Equilibrium binding of benzo(. alpha. )pyrene tetrol to synthetic polynucleotides: Sequence selectivity, thermodynamic properties, and ionic strength dependence

Journal Article · · Biochemistry; (USA)
DOI:https://doi.org/10.1021/bi00420a055· OSTI ID:6905872
; ;  [1]
  1. Univ. of California, San Francisco (USA)

The authors have investigated the equilibrium binding of racemic 7r,8t,9t,10c-tetrahydroxy-7,8,9,10-tetrahydrobenzo({alpha})pyrene to the double-stranded, synthetic polynucleotides poly(d(A-T)), poly(d(G-C)), and poly(d(G-m{sup 5}C)) at low binding ratios. Difference absorption spectroscopy shows a 10-nm red shift for binding to poly(d(A-T)) and an 11-nm red shift for binding to either poly(d(G-C)) or poly(d(G-m{sup 5}C)). The value of {Delta}{epsilon} for binding is approximately the same for all three hydrocarbon-polynucleotide complexes. Binding of this neutral polycyclic aromatic hydrocarbon derivative to these polynucleotides is dependent upon ionic strength and temperature. Analysis of complex formation employing polyelectrolyte theory shows a greater release of counterions associated with binding to poly(d(A-T)) than with the other two polynucleotides (0.5 and ca. 0.36, respectively). Thus, sequence-selective binding of this hydrocarbon in DNA would be expected to change dependent on salt concentration. The temperature dependence of binding was studied at 100 mM Na{sup +} where the equilibrium binding constants for poly(d(A-T)) and poly(d(G-m{sup 5}C)) are roughly equivalent and 6-fold greater than the binding affinity for poly(d(G-C)).

OSTI ID:
6905872
Journal Information:
Biochemistry; (USA), Vol. 27:20; ISSN 0006-2960
Country of Publication:
United States
Language:
English