Literature DB >> 2359460

Nucleation and growth of fibres and gel formation in sickle cell haemoglobin.

R E Samuel1, E D Salmon, R W Briehl.   

Abstract

Deoxygenated sickle haemoglobin polymerizes into long 210-A diameter fibres that distort and decrease the deformability of red blood cells, and cause sickle cell disease. The fibres consist of seven intertwined double strands. They can form birefringent nematic liquid crystals (tactoids) and spherulites. Rheologically, the system behaves as a gel. The equilibria show a phase separation and a solubility. The reaction kinetics show a delay time, are then roughly exponential and are highly dependent on concentration and temperature, and accord with the double nucleation model. But these conclusions are derived from macroscopic data, without direct observation of individual fibres. We have now used non-invasive video-enhanced differential interference contrast (DIC) and dark-field microscopy to observe nucleation, growth and interaction of sickle deoxyhaemoglobin fibres in real time. The fibres originate both from centres that produce many radially distributed fibres and on the surface of pre-existing fibres, from which they then branch. The resulting network is cross-linked and dynamic in that it is flexible and continues to grow and cross-link. Our results support most aspects of the double nucleation model.

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Year:  1990        PMID: 2359460     DOI: 10.1038/345833a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  30 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.  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.  Liquid-liquid separation in solutions of normal and sickle cell hemoglobin.

Authors:  Oleg Galkin; Kai Chen; Ronald L Nagel; Rhoda Elison Hirsch; Peter G Vekilov
Journal:  Proc Natl Acad Sci U S A       Date:  2002-06-17       Impact factor: 11.205

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

5.  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

6.  Quantifying the rheological and hemodynamic characteristics of sickle cell anemia.

Authors:  Huan Lei; George Em Karniadakis
Journal:  Biophys J       Date:  2012-01-18       Impact factor: 4.033

Review 7.  Tubulin depolymerization may be an ancient biological motor.

Authors:  J Richard McIntosh; Vladimir Volkov; Fazly I Ataullakhanov; Ekaterina L Grishchuk
Journal:  J Cell Sci       Date:  2010-10-15       Impact factor: 5.285

8.  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

9.  Fiber depolymerization: fracture, fragments, vanishing times, and stochastics in sickle hemoglobin.

Authors:  Jiang Cheng Wang; Suzanna Kwong; Frank A Ferrone; Matthew S Turner; Robin W Briehl
Journal:  Biophys J       Date:  2009-01       Impact factor: 4.033

10.  Simulated formation of polymer domains in sickle hemoglobin.

Authors:  Q Dou; F A Ferrone
Journal:  Biophys J       Date:  1993-11       Impact factor: 4.033

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