Literature DB >> 1244352

Resolution of erythrocyte membrane proteins by two-dimensional electrophoresis.

M J Conrad, J T Penniston.   

Abstract

A two-dimensional electrophoresis method has been developed which solubilizes erythrocyte membrane proteins, and which resolves the components of the band that migrates in detergent gels as if its molecular mass were 95,000 daltons. This method uses gel electrophoresis with sodium dodecyl sulfate in the first dimension and phenol, aqueous urea, and acetic acid in the second dimension. The 95,000 dalton band is known to contain several different membrane proteins, including those associated with anion transport, glucose transport, and (Na+,K+) transport. Two-dimensional electrophoresis resolved this band into one major spot and several minor ones. Pronase digestion of whole erythrocytes, followed by preparation of ghosts and two-dimensional electrophoresis, showed that only the major component of this band was digested by pronase.

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Year:  1976        PMID: 1244352

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  5 in total

1.  A novel system for the two-dimensional electrophoresis of membrane proteins.

Authors:  A G Booth
Journal:  Biochem J       Date:  1977-04-01       Impact factor: 3.857

Review 2.  Oligomeric structure and the anion transport function of human erythrocyte band 3 protein.

Authors:  M L Jennings
Journal:  J Membr Biol       Date:  1984       Impact factor: 1.843

3.  Gel electrophoresis of the human erythrocyte membrane proteins: aberrant patterns in hematological and non-hematological diseases.

Authors:  V Anselstetter
Journal:  Blut       Date:  1978-03-15

4.  Synthesis of tritiated 4,4'-diisothiocyano-2,2'-stilbene disulfonic acid ([3H]DIDS) and its covalent reaction with sites related to anion transport in human red blood cells.

Authors:  S Ship; Y Shami; W Breuer; A Rothstein
Journal:  J Membr Biol       Date:  1977-05-12       Impact factor: 1.843

5.  Peripheral proteins and smooth membrane from erythrocyte ghosts. Segregation of ATP-utilizing enzymes into smooth membrane.

Authors:  H Hayashi; H W Jarrett; J T Penniston
Journal:  J Cell Biol       Date:  1978-01       Impact factor: 10.539

  5 in total

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