Analysis of sedimentation equilibrium distributions reflecting nonideal macromolecular associations
- PMID: 11023922
- PMCID: PMC1301108
- DOI: 10.1016/S0006-3495(00)76466-6
Analysis of sedimentation equilibrium distributions reflecting nonideal macromolecular associations
Abstract
A rigorous statistical-mechanical approach is adopted to derive general quantitative expressions that allow for the effects of thermodynamic nonideality in equilibrium measurements reflecting interaction between dissimilar macromolecular reactants. An analytical procedure based on these expressions is then formulated for obtaining global estimates of equilibrium constants and the corresponding reference thermodynamic activities of the free reactants in each of several sedimentation equilibrium experiments. The method is demonstrated by application to results from an ultracentrifugal study of an electrostatic interaction between ovalbumin and cytochrome c (Winzor, D. J., M. P. Jacobsen, and P. R. Wills. 1998. Biochemistry. 37:2226-2233). It is demonstrated that reliable estimates of relevant thermodynamic parameters are extracted from the data through statistical analysis by means of a simple nonlinear fitting procedure.
Similar articles
-
A Hilly path through the thermodynamics and statistical mechanics of protein solutions.Biophys Rev. 2016 Dec;8(4):291-298. doi: 10.1007/s12551-016-0226-6. Epub 2016 Oct 25. Biophys Rev. 2016. PMID: 28510018 Free PMC article. Review.
-
Direct analysis of sedimentation equilibrium distributions reflecting complex formation between dissimilar reactants.Biochemistry. 1998 Feb 24;37(8):2226-33. doi: 10.1021/bi972211v. Biochemistry. 1998. PMID: 9485368
-
Direct analysis of sedimentation equilibrium distributions reflecting complex formation between cytochrome c and ovalbumin.Biochem Soc Trans. 1998 Nov;26(4):741-5. doi: 10.1042/bst0260741. Biochem Soc Trans. 1998. PMID: 10047818 No abstract available.
-
An ultracentrifugal approach to quantitative characterization of the molecular assembly of a physiological electron-transfer complex: the interaction of electron-transferring flavoprotein with trimethylamine dehydrogenase.Eur J Biochem. 1997 Jan 15;243(1-2):393-9. doi: 10.1111/j.1432-1033.1997.0393a.x. Eur J Biochem. 1997. PMID: 9030764
-
Interpreting the effects of small uncharged solutes on protein-folding equilibria.Annu Rev Biophys Biomol Struct. 2001;30:271-306. doi: 10.1146/annurev.biophys.30.1.271. Annu Rev Biophys Biomol Struct. 2001. PMID: 11340061 Review.
Cited by
-
A Hilly path through the thermodynamics and statistical mechanics of protein solutions.Biophys Rev. 2016 Dec;8(4):291-298. doi: 10.1007/s12551-016-0226-6. Epub 2016 Oct 25. Biophys Rev. 2016. PMID: 28510018 Free PMC article. Review.
-
Foreword to 'Quantitative and analytical relations in biochemistry'-a special issue in honour of Donald J. Winzor's 80th birthday.Biophys Rev. 2016 Dec;8(4):269-277. doi: 10.1007/s12551-016-0227-5. Epub 2016 Nov 4. Biophys Rev. 2016. PMID: 28510020 Free PMC article. Review.
-
Second virial coefficients as a measure of protein--osmolyte interactions.Protein Sci. 2001 Jan;10(1):12-6. doi: 10.1110/ps.29301. Protein Sci. 2001. PMID: 11266589 Free PMC article.
-
Comparison of methods for characterizing nonideal solute self-association by sedimentation equilibrium.Biophys J. 2009 Aug 5;97(3):886-96. doi: 10.1016/j.bpj.2009.05.028. Biophys J. 2009. PMID: 19651047 Free PMC article.
-
Measuring Ultra-Weak Protein Self-Association by Non-ideal Sedimentation Velocity.J Am Chem Soc. 2019 Feb 20;141(7):2990-2996. doi: 10.1021/jacs.8b11371. Epub 2019 Feb 6. J Am Chem Soc. 2019. PMID: 30668114 Free PMC article.
References
MeSH terms
Substances
LinkOut - more resources
Full Text Sources