Profound effects of electrolyte ions are observed on the kinetics and equilibria of DNA-protein interactions and DNA conformational changes. To understand the molecular and thermodynamic basis of these electrolyte effects, we propose to examine the equilibrium and dynamic behavior of ions and oligocation ligands in the vicinity of DNA, using quadrupolar cation NMR, Monte Carlo (MC) and analytical polyelectrolyte theories, and thermodynamic studies. We propose to obtain accurate descriptions of 1) the steep gradients in electrolyte ion concentrations in the vicinity of the DNA, 2) the local concentration and dynamic behavior of cations at the DNA surface, and 3) the thermodynamic consequences of the changes in these ion gradients that occur when the surface charge density of DNA is altered by conformational changes or by the binding of charged ligands, including proteins. Theoretical and experimental studies will be performed on polymeric DNA and on oligomers of defined chain length and sequences. Monte Carlo studies will be used to define the effects of experimental and modeling parameters on the details of the ion distribution as a function of oligomer chain length, and for the polymer limit. Quadrupolar NMR studies on suitable univalent cations will be performed to check MC predictions for the cation concentration at or near the DNA surface, and to explore the dynamics of these territorially bound ions. Thermodynamic functions and colligative coefficients for the polyelectrolyte solution will be obtained from MC ion distributions and compared with the results of the analytical polyelectrolyte theories. In particular, the polyelectrolyte-electrolyte preferential interaction parameter will be determined, and used in the analysis of electrolyte effects on the ligand-binding reactions and conformational equilibria of DNA. Small ions play a stoichiometric role as effectors or regulators of the equilibria and kinetics of the noncovalent interactions of biopolyelectrolytes in vitro. We propose to survey the range of mechanisms of stoichiometric regulation by small ions, and to examine the relevance of these mechanisms to the regulation of biopolyelectrolyte interactions in vivo, especially in eucaryotic cells where significant variations in intracellular ion concentrations have been observed during the cell cycle and in differentiation.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM034351-05
Application #
3285191
Study Section
Biophysics and Biophysical Chemistry A Study Section (BBCA)
Project Start
1984-12-01
Project End
1989-11-30
Budget Start
1988-12-01
Budget End
1989-11-30
Support Year
5
Fiscal Year
1989
Total Cost
Indirect Cost
Name
University of Wisconsin Madison
Department
Type
Schools of Arts and Sciences
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
Holbrook, J A; Capp, M W; Saecker, R M et al. (1999) Enthalpy and heat capacity changes for formation of an oligomeric DNA duplex: interpretation in terms of coupled processes of formation and association of single-stranded helices. Biochemistry 38:8409-22
Zhang, W; Ni, H; Capp, M W et al. (1999) The importance of coulombic end effects: experimental characterization of the effects of oligonucleotide flanking charges on the strength and salt dependence of oligocation (L8+) binding to single-stranded DNA oligomers. Biophys J 76:1008-17
Record Jr, M T; Courtenay, E S; Cayley, S et al. (1998) Biophysical compensation mechanisms buffering E. coli protein-nucleic acid interactions against changing environments. Trends Biochem Sci 23:190-4
Record Jr, M T; Zhang, W; Anderson, C F (1998) Analysis of effects of salts and uncharged solutes on protein and nucleic acid equilibria and processes: a practical guide to recognizing and interpreting polyelectrolyte effects, Hofmeister effects, and osmotic effects of salts. Adv Protein Chem 51:281-353
Padmanabhan, S; Zhang, W; Capp, M W et al. (1997) Binding of cationic (+4) alanine- and glycine-containing oligopeptides to double-stranded DNA: thermodynamic analysis of effects of coulombic interactions and alpha-helix induction. Biochemistry 36:5193-206
Zhang, W; Bond, J P; Anderson, C F et al. (1996) Large electrostatic differences in the binding thermodynamics of a cationic peptide to oligomeric and polymeric DNA. Proc Natl Acad Sci U S A 93:2511-6
Anderson, C F; Record Jr, M T (1995) Salt-nucleic acid interactions. Annu Rev Phys Chem 46:657-700
Olmsted, M C; Bond, J P; Anderson, C F et al. (1995) Grand canonical Monte Carlo molecular and thermodynamic predictions of ion effects on binding of an oligocation (L8+) to the center of DNA oligomers. Biophys J 68:634-47
Record Jr, M T; Anderson, C F (1995) Interpretation of preferential interaction coefficients of nonelectrolytes and of electrolyte ions in terms of a two-domain model. Biophys J 68:786-94
Bond, J P; Anderson, C F; Record Jr, M T (1994) Conformational transitions of duplex and triplex nucleic acid helices: thermodynamic analysis of effects of salt concentration on stability using preferential interaction coefficients. Biophys J 67:825-36

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