Literature DB >> 6928690

Electron microscope study of the kinetics of the fiber-to-crystal transition of sickle cell hemoglobin.

S M Wilson, M W Makinen.   

Abstract

The intermediates and the rate-limiting step in the crystallization of deoxygenated sickle hemoglobin have been determined by a kinetic study with the use of electron microscopy. In slowly stirred solutions of deoxygenated hemoglobin S [Pumphrey, J. & Steinhardt, J. (1977) J. Mol. Biol. 112, 359--375], the sequential appearance of fibers have a diameter of approximately equal to 210 A, bundles of aligned fibers in well-ordered arrays, "thick" fibers of approximately equal to 470 A diameter, and microcrystals is observed. Only the fibers having a diameter of approximately equal to 210 A and bundles of aligned fibers are assigned as kinetically important intermediates of the fiber-to-crystal transition. Addition of microscopic seed crystals obtained from slowly stirred solutions of deoxyhemoglobin S to a solution composed of only fibers and hemoglobin monomers results in more rapid crystallization than in control solutions. Addition of seed crystals after the formation of bindles of aligned fibers does not alter the overall kinetics of crystallization. The results demonstrate that alignment of fibers is the rate-limiting step in the crystallization process and results in formation of nucleation sites for crystal growth.

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Year:  1980        PMID: 6928690      PMCID: PMC348399          DOI: 10.1073/pnas.77.2.944

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  17 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.  Calorimetric and optical characterization of sickle cell hemoglobin gelation.

Authors:  P D Ross; J Hofrichter; W A Eaton
Journal:  J Mol Biol       Date:  1975-08-05       Impact factor: 5.469

3.  X-ray diffraction studies of fibers and crystals of deoxygenated sickle cell hemoglobin.

Authors:  B Magdoff-Fairchild; C C Chiu
Journal:  Proc Natl Acad Sci U S A       Date:  1979-01       Impact factor: 11.205

4.  Intermolecular organization of deoxygenated sickle haemoglobin determined by x-ray diffraction.

Authors:  B Magdoff-Fairchild; P H Swerdlow; J F Bertles
Journal:  Nature       Date:  1972-09-22       Impact factor: 49.962

5.  Structure of sickled erythrocytes and of sickle-cell hemoglobin fibers.

Authors:  J T Finch; M F Perutz; J F Bertles; J Döbler
Journal:  Proc Natl Acad Sci U S A       Date:  1973-03       Impact factor: 11.205

6.  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

7.  The fine structure of sickled hemoglobin in situ.

Authors:  J G White
Journal:  Blood       Date:  1968-05       Impact factor: 22.113

8.  Filtration characteristics of sickle cells: rates of alteration of filterability after deoxygenation and reoxygenation, and correlations with sickling and unsickling.

Authors:  M J Messer; J W Harris
Journal:  J Lab Clin Med       Date:  1970-10

9.  Crystallization of deoxyhemoglobin S by fiber alignment and fusion.

Authors:  T E Wellems; R Josephs
Journal:  J Mol Biol       Date:  1979-12-15       Impact factor: 5.469

10.  Augmentation of sickling process due to turbulent blood flow.

Authors:  P D Stein; H N Sabbah; A K Mandal
Journal:  J Appl Physiol       Date:  1976-01       Impact factor: 3.531

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  3 in total

1.  Rotation of sickle cells in homogeneous magnetic fields.

Authors:  P C Riberiro; M A Davidovich; E Wajnberg; G Bemski; M Kischinevsky
Journal:  Biophys J       Date:  1981-11       Impact factor: 4.033

2.  Triclinic crystals associated with fibers of deoxygenated sickle hemoglobin.

Authors:  B Magdoff-Fairchild; L S Rosen; C C Chiu
Journal:  EMBO J       Date:  1982       Impact factor: 11.598

3.  Hemoglobin interactions with αB crystallin: a direct test of sensitivity to protein instability.

Authors:  Tyler J W Clark; Scott A Houck; John I Clark
Journal:  PLoS One       Date:  2012-07-18       Impact factor: 3.240

  3 in total

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