Literature DB >> 7756545

Interpretation of preferential interaction coefficients of nonelectrolytes and of electrolyte ions in terms of a two-domain model.

M T Record1, C F Anderson.   

Abstract

For a three-component system consisting of solvent (1), polymer or polyelectrolyte (2J), and a nonelectrolyte or electrolyte solute (3), a two-domain description is developed to describe thermodynamic effects of interactions between solute components (2J) and (3). Equilibrium dialysis, which for an electrolyte solute produces the Donnan distribution of ions across a semipermeable membrane, provides a fundamental basis for this two-domain description whose applicability is not restricted, however, to systems where dialysis equilibrium is established. Explicit expressions are obtained for the solute-polymer preferential interaction coefficient gamma 3,2J (nonelectrolyte case) and for gamma +,2J and gamma -,2J, which are corresponding coefficients defined for single (univalent) cations and anions, respectively: gamma +,2J = magnitude of ZJ + gamma -,2J = 0.5(magnitude of ZJ + B-,2J + B+,2J) - B1,2Jm3/m1 Here B+,2J, B-,2J, and B1,2J are defined per mole of species J, respectively, as the number of moles of cation, anion, and water included within the local domains that surround isolated molecules of J; ZJ is the charge on J; m3 is the molal concentration of uniunivalent electrolyte, and m1 = 55.5 mol/kg for water. Incorporating this result into a general thermodynamic description(derived by us elsewhere) of the effects of the activity a+ of excess uniunivalent salt on an equilibrium involving two or more charged species J (each of which is dilute in comparison with the salt) yields:SaKobs bS/d a+ A(r+2J r 2j) A(B+2J B-2 2B12Jm3/m1)where KObS is an equilibrium quotient defined in terms of the molar concentrations of the participants, J, and A denotes astoichio metrically weighted combination of terms pertaining to the reactant(s) and product(s). The derivation presented here does not depend on any particular molecular model for salt-polyelectrolyte (or solute-polymer) interactions; it therefore generalizes our earlier (1978) derivation.

Entities:  

Mesh:

Substances:

Year:  1995        PMID: 7756545      PMCID: PMC1281802          DOI: 10.1016/S0006-3495(95)80254-7

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  8 in total

Review 1.  Water as ligand: preferential binding and exclusion of denaturants in protein unfolding.

Authors:  S N Timasheff
Journal:  Biochemistry       Date:  1992-10-20       Impact factor: 3.162

Review 2.  LINKED FUNCTIONS AND RECIPROCAL EFFECTS IN HEMOGLOBIN: A SECOND LOOK.

Authors:  J WYMAN
Journal:  Adv Protein Chem       Date:  1964

3.  Ion effects on ligand-nucleic acid interactions.

Authors:  M T Record; M L Lohman; P De Haseth
Journal:  J Mol Biol       Date:  1976-10-25       Impact factor: 5.469

4.  A simple model for solvation in mixed solvents. Applications to the stabilization and destabilization of macromolecular structures.

Authors:  J A Schellman
Journal:  Biophys Chem       Date:  1990-08-31       Impact factor: 2.352

Review 5.  Thermodynamic analysis of ion effects on the binding and conformational equilibria of proteins and nucleic acids: the roles of ion association or release, screening, and ion effects on water activity.

Authors:  M T Record; C F Anderson; T M Lohman
Journal:  Q Rev Biophys       Date:  1978-05       Impact factor: 5.318

6.  Preferential and absolute interactions of solvent components with proteins in mixed solvent systems.

Authors:  H Inoue; S N Timasheff
Journal:  Biopolymers       Date:  1972       Impact factor: 2.505

7.  Extension of the theory of linked functions to incorporate the effects of protein hydration.

Authors:  C Tanford
Journal:  J Mol Biol       Date:  1969-02-14       Impact factor: 5.469

8.  The thermodynamics of solvent exchange.

Authors:  J A Schellman
Journal:  Biopolymers       Date:  1994-08       Impact factor: 2.505

  8 in total
  36 in total

1.  Assessing accumulated solvent near a macromolecular solute by preferential interaction coefficients.

Authors:  Karen E S Tang; Victor A Bloomfield
Journal:  Biophys J       Date:  2002-06       Impact factor: 4.033

2.  Quantifying why urea is a protein denaturant, whereas glycine betaine is a protein stabilizer.

Authors:  Emily J Guinn; Laurel M Pegram; Michael W Capp; Michelle N Pollock; M Thomas Record
Journal:  Proc Natl Acad Sci U S A       Date:  2011-09-19       Impact factor: 11.205

3.  Probing protein hydration and conformational states in solution.

Authors:  C Reid; R P Rand
Journal:  Biophys J       Date:  1997-03       Impact factor: 4.033

4.  Protein-solvent preferential interactions, protein hydration, and the modulation of biochemical reactions by solvent components.

Authors:  Serge N Timasheff
Journal:  Proc Natl Acad Sci U S A       Date:  2002-07-03       Impact factor: 11.205

5.  Protein stability in mixed solvents: a balance of contact interaction and excluded volume.

Authors:  John A Schellman
Journal:  Biophys J       Date:  2003-07       Impact factor: 4.033

6.  A contribution to the theory of preferential interaction coefficients.

Authors:  J Michael Schurr; David P Rangel; Sergio R Aragon
Journal:  Biophys J       Date:  2005-07-29       Impact factor: 4.033

7.  Chemical potential derivatives and preferential interaction parameters in biological systems from Kirkwood-Buff theory.

Authors:  Paul E Smith
Journal:  Biophys J       Date:  2006-05-05       Impact factor: 4.033

Review 8.  Recent applications of Kirkwood-Buff theory to biological systems.

Authors:  Veronica Pierce; Myungshim Kang; Mahalaxmi Aburi; Samantha Weerasinghe; Paul E Smith
Journal:  Cell Biochem Biophys       Date:  2007-11-28       Impact factor: 2.194

9.  Thermodynamic and structural basis for relaxation of specificity in protein-DNA recognition.

Authors:  Paul J Sapienza; Tianyi Niu; Michael R Kurpiewski; Arabela Grigorescu; Linda Jen-Jacobson
Journal:  J Mol Biol       Date:  2013-09-14       Impact factor: 5.469

10.  Crowder-Induced Conformational Ensemble Shift in Escherichia coli Prolyl-tRNA Synthetase.

Authors:  Lauren M Adams; Ryan J Andrews; Quin H Hu; Heidi L Schmit; Sanchita Hati; Sudeep Bhattacharyya
Journal:  Biophys J       Date:  2019-08-31       Impact factor: 4.033

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.