Literature DB >> 28510163

Ratchets, red cells, and metastability.

Frank A Ferrone1, Alexey Aprelev2.   

Abstract

Sickle cell disease is a genetic disorder in which a negatively charged glutamic acid is replaced by a hydrophobic valine on the surface of the hemoglobin molecule, leading to polymerization of the deoxygenated form, and resulting in microvascular obstruction. Because of the high volume occupancy under which polymerization occurs physiologically, this process has been an exemplar in the study of excluded volume effects on assembly. More recently, we have identified yet another type of crowding effect involving the obstruction of the ends at which the polymers grow as a consequence of the dense arrays in which these polymers form. This makes such solutions metastable, and leads to Brownian ratchet behavior in which pressure is exerted outward when the gel occupies a finite volume, as in an emulsion or red cell. Such behavior is capable of holding sickled cells in place in the microcirculation against weak pressure differentials (hundreds of Pa), but not against the typical pressures found in vivo.

Entities:  

Keywords:  Brownian ratchet; Molecular crowding; Polymerization; Sickle cell disease

Year:  2013        PMID: 28510163      PMCID: PMC5425722          DOI: 10.1007/s12551-013-0117-z

Source DB:  PubMed          Journal:  Biophys Rev        ISSN: 1867-2450


  22 in total

Review 1.  Crowding and the polymerization of sickle hemoglobin.

Authors:  Frank A Ferrone; Maria A Rotter
Journal:  J Mol Recognit       Date:  2004 Sep-Oct       Impact factor: 2.137

2.  The kinetics of nucleation and growth of sickle cell hemoglobin fibers.

Authors:  Oleg Galkin; Ronald L Nagel; Peter G Vekilov
Journal:  J Mol Biol       Date:  2006-10-05       Impact factor: 5.469

3.  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

4.  Gelation of sickle cell hemoglobin in mixtures with normal adult and fetal hemoglobins.

Authors:  H R Sunshine; J Hofrichter; W A Eaton
Journal:  J Mol Biol       Date:  1979-10-09       Impact factor: 5.469

5.  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

Review 6.  Hemoglobin S gelation and sickle cell disease.

Authors:  W A Eaton; J Hofrichter
Journal:  Blood       Date:  1987-11       Impact factor: 22.113

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.  Carbon monoxide religation kinetics to hemoglobin S polymers following ligand photolysis.

Authors:  D B Shapiro; R M Esquerra; R A Goldbeck; S K Ballas; N Mohandas; D S Kliger
Journal:  J Biol Chem       Date:  1995-11-03       Impact factor: 5.157

9.  Microvascular pressure and functional capillary density in extreme hemodilution with low- and high-viscosity dextran and a low-viscosity Hb-based O2 carrier.

Authors:  Pedro Cabrales; Amy G Tsai; Marcos Intaglietta
Journal:  Am J Physiol Heart Circ Physiol       Date:  2004-02-19       Impact factor: 4.733

10.  Universal metastability of sickle hemoglobin polymerization.

Authors:  Weijun Weng; Alexey Aprelev; Robin W Briehl; Frank A Ferrone
Journal:  J Mol Biol       Date:  2008-02-05       Impact factor: 5.469

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