Literature DB >> 18308336

Universal metastability of sickle hemoglobin polymerization.

Weijun Weng1, Alexey Aprelev, Robin W Briehl, Frank A Ferrone.   

Abstract

Sickle hemoglobin (HbS) polymerization occurs when the concentration of deoxyHbS exceeds a well-defined solubility. In experiments using sickle hemoglobin droplets suspended in oil, it has been shown that when polymerization ceases the monomer concentration is above equilibrium solubility. We find that the final concentration in uniform bulk solutions (i.e., with negligible boundaries) agrees with the droplet measurements, and both exceed the expected solubility. To measure hemoglobin in uniform solutions, we used modulated excitation of trace amounts of CO in gels of HbS. In this method, a small amount of CO is introduced to a spatially uniform deoxyHb sample, so that less than 2% of the sample is liganded. The liganded fraction is photolyzed repeatedly and the rate of recombination allows the concentration of deoxyHbS in the solution phase to be determined, even if polymers have formed. Both uniform and droplet samples exhibit the same quantitative behavior, exceeding solubility by an amount that depends on the initial concentration of the sample, as well as conditions under which the gel was formed. We hypothesize that the early termination of polymerization is due to the obstruction in polymer growth, which is consistent with the observation that pressing on slides lowers the final monomer concentration, making it closer to solubility. The thermodynamic solubility in free solution is thus achieved only in conditions with low polymer density or under external forces (such as found in sedimentation) that disrupt polymers. Since we find that only about 67% of the expected polymer mass forms, this result will impact any analysis predicated on predicting the polymer fraction in a given experiment.

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Year:  2008        PMID: 18308336      PMCID: PMC2430085          DOI: 10.1016/j.jmb.2008.01.083

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


  23 in total

1.  Supersaturation in sickle cell hemoglobin solutions.

Authors:  J Hofrichter; P D Ross; W A Eaton
Journal:  Proc Natl Acad Sci U S A       Date:  1976-09       Impact factor: 11.205

2.  The force generated by biological membranes on a polymer rod and its response: statics and dynamics.

Authors:  D R Daniels; M S Turner
Journal:  J Chem Phys       Date:  2004-10-15       Impact factor: 3.488

3.  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

4.  Solubility of sickle hemoglobin measured by a kinetic micromethod.

Authors:  D Liao; J J Martin de Llano; J P Himanen; J M Manning; F A Ferrone
Journal:  Biophys J       Date:  1996-05       Impact factor: 4.033

5.  Kinetics and mechanism of deoxyhemoglobin S gelation: a new approach to understanding sickle cell disease.

Authors:  J Hofrichter; P D Ross; W A Eaton
Journal:  Proc Natl Acad Sci U S A       Date:  1974-12       Impact factor: 11.205

6.  Effects of pH, 2,3-diphosphoglycerate and salts on gelation of sickle cell deoxyhemoglobin.

Authors:  R W Briehl; S Ewert
Journal:  J Mol Biol       Date:  1973-11-05       Impact factor: 5.469

7.  Modulated excitation of singly ligated carboxyhemoglobin.

Authors:  D Liao; J Jiang; M Zhao; F A Ferrone
Journal:  Biophys J       Date:  1993-11       Impact factor: 4.033

8.  Sickle cell rheology is determined by polymer fraction--not cell morphology.

Authors:  H Hiruma; C T Noguchi; N Uyesaka; S Hasegawa; E J Blanchette-Mackie; A N Schechter; G P Rodgers
Journal:  Am J Hematol       Date:  1995-01       Impact factor: 10.047

9.  Oxygen binding by sickle cell hemoglobin polymers.

Authors:  H R Sunshine; J Hofrichter; F A Ferrone; W A Eaton
Journal:  J Mol Biol       Date:  1982-06-25       Impact factor: 5.469

10.  Hemoglobin S polymerization: primary determinant of the hemolytic and clinical severity of the sickling syndromes.

Authors:  G M Brittenham; A N Schechter; C T Noguchi
Journal:  Blood       Date:  1985-01       Impact factor: 22.113

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  6 in total

1.  The microrheology of sickle hemoglobin gels.

Authors:  Mikhail N Zakharov; Alexey Aprelev; Matthew S Turner; Frank A Ferrone
Journal:  Biophys J       Date:  2010-08-09       Impact factor: 4.033

Review 2.  Ratchets, red cells, and metastability.

Authors:  Frank A Ferrone; Alexey Aprelev
Journal:  Biophys Rev       Date:  2013-04-18

3.  The physical foundation of vasoocclusion in sickle cell disease.

Authors:  Alexey Aprelev; William Stephenson; Hongseok Moses Noh; Maureen Meier; Frank A Ferrone
Journal:  Biophys J       Date:  2012-10-16       Impact factor: 4.033

4.  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

5.  The growth of sickle hemoglobin polymers.

Authors:  Alexey Aprelev; Zenghui Liu; Frank A Ferrone
Journal:  Biophys J       Date:  2011-08-17       Impact factor: 4.033

Review 6.  Impact of hemoglobin biophysical studies on molecular pathogenesis and drug therapy for sickle cell disease.

Authors:  William A Eaton
Journal:  Mol Aspects Med       Date:  2021-07-14
  6 in total

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