Literature DB >> 7756551

Analyses of thermodynamic data for concentrated hemoglobin solutions using scaled particle theory: implications for a simple two-state model of water in thermodynamic analyses of crowding in vitro and in vivo.

H J Guttman1, C F Anderson, M T Record.   

Abstract

Quantitative description of the thermodynamic consequences of macromolecular crowding (excluded volume nonideality) is an important component of analyses of the thermodynamics and kinetics of noncovalent interactions of biopolymers in vivo and in concentrated polymer solutions in vitro. By analyzing previously published thermodynamic data, we have investigated extensively the comparative applicability of two forms of scaled particle theory (SPT). In both forms, macromolecules are treated as hard spheres, but MSPT, introduced by Ross and Minton, treats the solvent as a structureless continuum, whereas bulk water molecules are included explicitly as hard spheres in BSPT, an approach developed by Berg. Here we use both MSPT and BSPT to calculate the excluded volume component of the macromolecular activity coefficient of hemoglobin (Hb) at concentrations up to 509 mg/ml by fitting osmotic pressure data for Hb and sedimentation equilibrium data for Hb and sickle-cell Hb (HbS). Both forms of SPT also are used here to analyze the effects of other globular proteins (BSA and Hb) on the solubility of HbS. In applying MSPT and BSPT to analyze macromolecular crowding, the extent of hydration delta Hb (in gH2O/gprotein) is introduced as an adjustable parameter to specify the effective (hard sphere) radius of hydrated Hb. In our nonlinear least-squares fittings based on BSPT, the hard sphere radius of bulk water molecules is either fixed at 1.375 A or floated. Although both forms of SPT yield good fittings (with different values of delta Hb) at Hb concentrations up to 350 mg/ml, only BSPT gives good fittings of all available Hb osmotic pressure data as well as of the sedimentation equilibrium and solubility data. Only BSPT predicts values for delta Hb (approximately 0.5-0.6 g/g) in the range obtained for Hb from hydrodynamic measurements (approximately 0.36-0.78 g/g). These findings indicate the applicability, at least in the context of BSPT, of a simple two-state classification of water (bulk water and water of macromolecular hydration) as a basis for interpreting excluded volume nonideality in concentrated solutions of globular proteins.

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Year:  1995        PMID: 7756551      PMCID: PMC1281808          DOI: 10.1016/S0006-3495(95)80260-2

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


  15 in total

1.  The effect of non-aggregating proteins upon the gelation of sickle cell hemoglobin: model calculations and data analysis.

Authors:  P D Ross; A P Minton
Journal:  Biochem Biophys Res Commun       Date:  1979-06-27       Impact factor: 3.575

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Authors:  F Vérétout; M Delaye; A Tardieu
Journal:  J Mol Biol       Date:  1989-02-20       Impact factor: 5.469

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Journal:  Adv Protein Chem       Date:  1974

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Authors:  S Leikin; D C Rau; V A Parsegian
Journal:  Proc Natl Acad Sci U S A       Date:  1994-01-04       Impact factor: 11.205

5.  The effect of volume occupancy upon the thermodynamic activity of proteins: some biochemical consequences.

Authors:  A P Minton
Journal:  Mol Cell Biochem       Date:  1983       Impact factor: 3.396

6.  Temperature dependence of nonideality in concentrated solutions of hemoglobin.

Authors:  P D Ross; R W Briehl; A P Minton
Journal:  Biopolymers       Date:  1978-09       Impact factor: 2.505

Review 7.  How crowded is the cytoplasm?

Authors:  A B Fulton
Journal:  Cell       Date:  1982-09       Impact factor: 41.582

8.  Thermodynamic nonideality and the dependence of partition coefficient upon solute concentration in exclusion chromatography. Application to self-associating and non-self-associating solutes. Application to hemoglobin.

Authors:  A P Minton
Journal:  Biophys Chem       Date:  1980-12       Impact factor: 2.352

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Authors:  P G Squire; M E Himmel
Journal:  Arch Biochem Biophys       Date:  1979-08       Impact factor: 4.013

10.  Sickle hemoglobin gelation. Reaction order and critical nucleus size.

Authors:  M J Behe; S W Englander
Journal:  Biophys J       Date:  1978-07       Impact factor: 4.033

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  8 in total

1.  Direct observation of the enhancement of noncooperative protein self-assembly by macromolecular crowding: indefinite linear self-association of bacterial cell division protein FtsZ.

Authors:  G Rivas; J A Fernández; A P Minton
Journal:  Proc Natl Acad Sci U S A       Date:  2001-03-13       Impact factor: 11.205

2.  COVOL: an interactive program for evaluating second virial coefficients from the triaxial shape or dimensions of rigid macromolecules.

Authors:  S E Harding; J C Horton; S Jones; J M Thornton; D J Winzor
Journal:  Biophys J       Date:  1999-05       Impact factor: 4.033

3.  Excluded volume in solvation: sensitivity of scaled-particle theory to solvent size and density.

Authors:  K E Tang; V A Bloomfield
Journal:  Biophys J       Date:  2000-11       Impact factor: 4.033

4.  The role of macromolecular crowding in the evolution of lens crystallins with high molecular refractive index.

Authors:  Huaying Zhao; M Teresa Magone; Peter Schuck
Journal:  Phys Biol       Date:  2011-05-12       Impact factor: 2.583

5.  Biophysical characterization of changes in amounts and activity of Escherichia coli cell and compartment water and turgor pressure in response to osmotic stress.

Authors:  D S Cayley; H J Guttman; M T Record
Journal:  Biophys J       Date:  2000-04       Impact factor: 4.033

6.  Basis of Protein Stabilization by K Glutamate: Unfavorable Interactions with Carbon, Oxygen Groups.

Authors:  Xian Cheng; Emily J Guinn; Evan Buechel; Rachel Wong; Rituparna Sengupta; Irina A Shkel; M Thomas Record
Journal:  Biophys J       Date:  2016-11-01       Impact factor: 4.033

7.  Characterization of the hypertonically induced tyrosine phosphorylation of erythrocyte band 3.

Authors:  G Minetti; C Seppi; A Ciana; C Balduini; P S Low; A Brovelli
Journal:  Biochem J       Date:  1998-10-15       Impact factor: 3.857

8.  The Effect of Attractive Interactions and Macromolecular Crowding on Crystallins Association.

Authors:  Jiachen Wei; Jure Dobnikar; Tine Curk; Fan Song
Journal:  PLoS One       Date:  2016-03-08       Impact factor: 3.240

  8 in total

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