Literature DB >> 4916314

Gels of normal and sickled hemoglobin: comparative study.

J G White, B Heagan.   

Abstract

Electron microscopic studies of the sickling phenomenon have described at least three different structural arrangements of sickled hemoglobin, including empty hexagonal crystals, microtubules, and solid rods. It is unlikely that sickling results in several different polymers, and it is essential to determine the true structure of sickled hemoglobin in order to define the mechanism of molecular assembly. The present study has explored the fine structure of gels formed in cell-free solutions of normal and sickle reduced and oxyhemoglobin. Gels of reduced sickled hemoglobin consisted entirely of solid rods. The gels formed from sickle oxyhemoglobin, normal oxyhemoglobin, and normal reduced hemoglobin contained masses of hollow polymers essentially identical in appearance with microtubules. These findings indicate that solid rods are the characteristic polymers of sickled hemoglobin and tubular polymers represent aberrant structures which are not related to erythrocyte sickling.

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Year:  1970        PMID: 4916314      PMCID: PMC2138839          DOI: 10.1084/jem.131.6.1079

Source DB:  PubMed          Journal:  J Exp Med        ISSN: 0022-1007            Impact factor:   14.307


  9 in total

1.  A simplified technique for a large scale crystallization of human oxyhemoglobin; isomorphous transformations of hemoglobin and myoglobin in the crystalline state.

Authors:  D L DRABKIN
Journal:  Arch Biochem       Date:  1949-03

2.  Studies on the destruction of red blood cells. VIII. Molecular orientation in sickle cell hemoglobin solutions.

Authors:  J W HARRIS
Journal:  Proc Soc Exp Biol Med       Date:  1950-10

3.  Sickle cell anemia a molecular disease.

Authors:  L PAULING; H A ITANO
Journal:  Science       Date:  1949-11-25       Impact factor: 47.728

4.  The fine structure of sickled hemoglobin in situ.

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

5.  Observations on the mechanism of erythrocyte sickling.

Authors:  J G White
Journal:  Pediatr Res       Date:  1969-05       Impact factor: 3.756

6.  Reversible and irreversible sickling: a distinction by electron microscopy.

Authors:  J F Bertles; J Döbler
Journal:  Blood       Date:  1969-06       Impact factor: 22.113

7.  Molecular mechanism of red cell "sickling".

Authors:  M Murayama
Journal:  Science       Date:  1966-07-08       Impact factor: 47.728

8.  The physical state of hemoglobin in sickle-cell anemia erythrocytes in vivo.

Authors:  J Döbler; J F Bertles
Journal:  J Exp Med       Date:  1968-04-01       Impact factor: 14.307

9.  The state of hemoglobin in sickled erythrocytes.

Authors:  C A Stetson
Journal:  J Exp Med       Date:  1966-02-01       Impact factor: 14.307

  9 in total
  4 in total

1.  Dissecting the energies that stabilize sickle hemoglobin polymers.

Authors:  Yihua Wang; Frank A Ferrone
Journal:  Biophys J       Date:  2013-11-05       Impact factor: 4.033

2.  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

3.  In vitro effects of anthocyanin extracts from Justicia secunda Vahl on the solubility of haemoglobin S and membrane stability of sickle erythrocytes.

Authors:  Pius T Mpiana; KotoTe Niwa N Ngbolua; Matthieu T Bokota; Teddy K Kasonga; Emmanuel K Atibu; Damien S T Tshibangu; Virima Mudogo
Journal:  Blood Transfus       Date:  2010-10       Impact factor: 3.443

4.  A new antisickling agent: in vitro studies of its effect on S/S erythrocytes and on hemoglobin S.

Authors:  P K Adhikary; J K Haynes; H L Patthey; R S Rhodes
Journal:  Experientia       Date:  1978-06-15
  4 in total

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