Literature DB >> 4046025

Chemical potential measurements of deoxyhemoglobin S polymerization. Determination of the phase diagram of an assembling protein.

M S Prouty, A N Schechter, V A Parsegian.   

Abstract

We have used the "osmotic stress" method to determine the phase diagram of deoxyhemoglobin S polymerization. This method involves equilibration, through a semipermeable membrane, of the protein with solutions of inert polymers of known osmotic pressure. With deoxyhemoglobin A and S solutions, in which we have demonstrated achievement of equilibrium, plots of osmotic pressure versus concentration initially agree closely with the results of other methods of measurement of colligative properties. However, once the known solubility value is exceeded for the deoxyhemoglobin S solutions at various temperatures, there is a rapid rise in hemoglobin concentration over a narrow osmotic pressure range and then a more gradual increase in concentration. We believe that these two regions correspond, respectively, to the onset of the polymerization process, and of subsequent continuing growth and compression or alignment of polymer. We derive the thermodynamic values for these processes and show that the behavior of the deoxyhemoglobin S system is analogous to the phase transition for a simple chemical system. These results are relevant to understanding the intracellular polymerization of deoxyhemoglobin S in sickle cell disease, and these concepts are applicable to other protein assembly systems.

Entities:  

Mesh:

Substances:

Year:  1985        PMID: 4046025     DOI: 10.1016/0022-2836(85)90298-0

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  23 in total

1.  Osmotic stress, crowding, preferential hydration, and binding: A comparison of perspectives.

Authors:  V A Parsegian; R P Rand; D C Rau
Journal:  Proc Natl Acad Sci U S A       Date:  2000-04-11       Impact factor: 11.205

2.  Heterogeneous nucleation and crowding in sickle hemoglobin: an analytic approach.

Authors:  Frank A Ferrone; Maria Ivanova; Ravi Jasuja
Journal:  Biophys J       Date:  2002-01       Impact factor: 4.033

3.  Intermolecular interactions, nucleation, and thermodynamics of crystallization of hemoglobin C.

Authors:  Peter G Vekilov; Angela R Feeling-Taylor; Dimiter N Petsev; Oleg Galkin; Ronald L Nagel; Rhoda Elison Hirsch
Journal:  Biophys J       Date:  2002-08       Impact factor: 4.033

4.  Monomer diffusion and polymer alignment in domains of sickle hemoglobin.

Authors:  M R Cho; F A Ferrone
Journal:  Biophys J       Date:  1992-07       Impact factor: 4.033

Review 5.  Protein interactions in the calf eye lens: interactions between beta-crystallins are repulsive whereas in gamma-crystallins they are attractive.

Authors:  A Tardieu; F Vérétout; B Krop; C Slingsby
Journal:  Eur Biophys J       Date:  1992       Impact factor: 1.733

6.  Direct measurement of the intermolecular forces between counterion-condensed DNA double helices. Evidence for long range attractive hydration forces.

Authors:  D C Rau; V A Parsegian
Journal:  Biophys J       Date:  1992-01       Impact factor: 4.033

7.  Direct measurement of temperature-dependent solvation forces between DNA double helices.

Authors:  D C Rau; V A Parsegian
Journal:  Biophys J       Date:  1992-01       Impact factor: 4.033

8.  Static light scattering from concentrated protein solutions, I: General theory for protein mixtures and application to self-associating proteins.

Authors:  Allen P Minton
Journal:  Biophys J       Date:  2007-05-25       Impact factor: 4.033

9.  Osmotic effects of protein polymerization: analysis of volume changes in sickle cell anemia red cells following deoxy-hemoglobin S polymerization.

Authors:  V L Lew; R M Bookchin
Journal:  J Membr Biol       Date:  1991-05       Impact factor: 1.843

10.  Solid-liquid phase boundaries of lens protein solutions.

Authors:  C R Berland; G M Thurston; M Kondo; M L Broide; J Pande; O Ogun; G B Benedek
Journal:  Proc Natl Acad Sci U S A       Date:  1992-02-15       Impact factor: 11.205

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.