Literature DB >> 3947628

Radiation inactivation of the human erythrocyte nucleoside and glucose transporters.

S M Jarvis, J C Ellory, J D Young.   

Abstract

The human erythrocyte nucleoside and glucose transporters, identified previously as band 4.5 peptides (apparent Mr 66 000-45 000) on SDS-polyacrylamide gels, have been characterized in situ by radiation inactivation analysis. Target size analysis of lyophilized membranes indicates an apparent Mr of 110 000 +/- 12 000 and 124 000 +/- 11 000 for the nucleoside and glucose carriers, respectively. These data suggest that both transporters exist in the membrane as dimers.

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Year:  1986        PMID: 3947628     DOI: 10.1016/0005-2736(86)90179-3

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  4 in total

1.  Inhibition by nucleosides of glucose-transport activity in human erythrocytes.

Authors:  S M Jarvis
Journal:  Biochem J       Date:  1988-01-15       Impact factor: 3.857

2.  Reconciling contradictory findings: Glucose transporter 1 (GLUT1) functions as an oligomer of allosteric, alternating access transporters.

Authors:  Kenneth P Lloyd; Ogooluwa A Ojelabi; Julie K De Zutter; Anthony Carruthers
Journal:  J Biol Chem       Date:  2017-10-24       Impact factor: 5.157

3.  Interaction of [3H]dipyridamole with the nucleoside transporters of human erythrocytes and cultured animal cells.

Authors:  C Woffendin; P G Plagemann
Journal:  J Membr Biol       Date:  1987       Impact factor: 1.843

4.  Monoclonal antibodies possibly recognize conformational changes in the human erythrocyte glucose transporter.

Authors:  H Nishimura; H Kuzuya; A Kosaki; M Okamoto; M Okamoto; S Kono; G Inoue; I Maeda; H Imura
Journal:  Biochem J       Date:  1992-01-01       Impact factor: 3.857

  4 in total

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