Literature DB >> 11751326

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

Frank A Ferrone1, Maria Ivanova, Ravi Jasuja.   

Abstract

Sickle hemoglobin nucleation occurs in solution as a homogeneous process or on existing polymers in a heterogeneous process. We have developed an analytic formulation to describe the solution crowding and large nonideality that affects the heterogeneous nucleation of sickle hemoglobin by using convex particle theory. The formulation successfully fits the concentration and temperature dependence of the heterogeneous nucleation process over 14 orders of magnitude. Unlike previous approaches, however, the new formulation can also accurately describe the effects of adding nonpolymerizing agents to the solution. Without additional adjustable parameters, the model now describes the data of M. Ivanova, R. Jasuja, S. Kwong, R. W. Briehl, and F. A. Ferrone, (Biophys. J. 2000, 79:1016-1022), in which up to 50% of the sickle hemoglobin is substituted by cross-linked hemoglobin A, which does not polymerize, and which substitution causes the rates to decrease by 10(5). The success of this approach provides insight into the polymerization process: from the size-dependence of the contact energy deduced here, it also appears that various contacts of unknown origin are energetically significant in the heterogeneous nucleation process.

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Year:  2002        PMID: 11751326      PMCID: PMC1302479          DOI: 10.1016/S0006-3495(02)75404-0

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


  19 in total

1.  Nonideality and the nucleation of sickle hemoglobin.

Authors:  M Ivanova; R Jasuja; S Kwong; R W Briehl; F A Ferrone
Journal:  Biophys J       Date:  2000-08       Impact factor: 4.033

2.  Thermodynamics of gelation of sickle cell deoxyhemoglobin.

Authors:  P D Ross; J Hofrichter; W A Eaton
Journal:  J Mol Biol       Date:  1977-09-15       Impact factor: 5.469

3.  Analysis of non-ideal behavior in concentrated hemoglobin solutions.

Authors:  P D Ross; A P Minton
Journal:  J Mol Biol       Date:  1977-05-25       Impact factor: 5.469

4.  Intermolecular contacts within sickle hemoglobin fibers.

Authors:  S J Watowich; L J Gross; R Josephs
Journal:  J Mol Biol       Date:  1989-10-20       Impact factor: 5.469

5.  Kinetics of nucleation-controlled polymerization. A perturbation treatment for use with a secondary pathway.

Authors:  M F Bishop; F A Ferrone
Journal:  Biophys J       Date:  1984-11       Impact factor: 4.033

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

7.  Kinetics of sickle hemoglobin polymerization. I. Studies using temperature-jump and laser photolysis techniques.

Authors:  F A Ferrone; J Hofrichter; W A Eaton
Journal:  J Mol Biol       Date:  1985-06-25       Impact factor: 5.469

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

Authors:  M S Prouty; A N Schechter; V A Parsegian
Journal:  J Mol Biol       Date:  1985-08-05       Impact factor: 5.469

9.  Kinetic studies on photolysis-induced gelation of sickle cell hemoglobin suggest a new mechanism.

Authors:  F A Ferrone; J Hofrichter; H R Sunshine; W A Eaton
Journal:  Biophys J       Date:  1980-10       Impact factor: 4.033

10.  Kinetics of sickle hemoglobin polymerization. II. A double nucleation mechanism.

Authors:  F A Ferrone; J Hofrichter; W A Eaton
Journal:  J Mol Biol       Date:  1985-06-25       Impact factor: 5.469

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  14 in total

1.  Life in a crowded world.

Authors:  Germán Rivas; Frank Ferrone; Judith Herzfeld
Journal:  EMBO Rep       Date:  2004-01       Impact factor: 8.807

2.  Understanding the shape of sickled red cells.

Authors:  Garrott W Christoph; James Hofrichter; William A Eaton
Journal:  Biophys J       Date:  2004-11-12       Impact factor: 4.033

3.  Heterogeneous nucleation in sickle hemoglobin: experimental validation of a structural mechanism.

Authors:  Maria A Rotter; Suzanna Kwong; Robin W Briehl; Frank A Ferrone
Journal:  Biophys J       Date:  2005-07-29       Impact factor: 4.033

4.  Metastable polymerization of sickle hemoglobin in droplets.

Authors:  Alexey Aprelev; Weijun Weng; Mikhail Zakharov; Maria Rotter; Donna Yosmanovich; Suzanna Kwong; Robin W Briehl; Frank A Ferrone
Journal:  J Mol Biol       Date:  2007-04-19       Impact factor: 5.469

5.  Potential of Three Ethnomedicinal Plants as Antisickling Agents.

Authors:  Ismaila O Nurain; Clement O Bewaji; Jarrett S Johnson; Robertson D Davenport; Yang Zhang
Journal:  Mol Pharm       Date:  2016-12-05       Impact factor: 4.939

6.  Universality of supersaturation in protein-fiber formation.

Authors:  Troy Cellmer; Frank A Ferrone; William A Eaton
Journal:  Nat Struct Mol Biol       Date:  2016-03-28       Impact factor: 15.369

7.  Theoretical Simulation of Red Cell Sickling Upon Deoxygenation Based on the Physical Chemistry of Sickle Hemoglobin Fiber Formation.

Authors:  Emily B Dunkelberger; Belhu Metaferia; Troy Cellmer; Eric R Henry
Journal:  J Phys Chem B       Date:  2018-09-18       Impact factor: 2.991

8.  Band 3 catalyzes sickle hemoglobin polymerization.

Authors:  Maria A Rotter; Haiyan Chu; Philip S Low; Frank A Ferrone
Journal:  Biophys Chem       Date:  2009-10-19       Impact factor: 2.352

9.  Deciphering Copper Coordination in the Mammalian Prion Protein Amyloidogenic Domain.

Authors:  Giulia Salzano; Martha Brennich; Giordano Mancini; Thanh Hoa Tran; Giuseppe Legname; Paola D'Angelo; Gabriele Giachin
Journal:  Biophys J       Date:  2020-01-03       Impact factor: 4.033

10.  Nucleated polymerization with secondary pathways. I. Time evolution of the principal moments.

Authors:  Samuel I A Cohen; Michele Vendruscolo; Mark E Welland; Christopher M Dobson; Eugene M Terentjev; Tuomas P J Knowles
Journal:  J Chem Phys       Date:  2011-08-14       Impact factor: 3.488

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