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PMID: 1244352 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Resolution of erythrocyte membrane proteins by two-dimensional electrophoresis.

The Journal of biological chemistry ·Vol. 251 ·No. 1 ·1976-01-10 ·Pages 253-5

Conrad MJ, Penniston JT

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.

MeSH Terms
Blood Proteins/isolation & purification Cell Membrane/analysis Electrophoresis, Polyacrylamide Gel Erythrocytes/analysis Humans
Chemicals
Blood Proteins
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Conrad M J
Penniston J T
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1976-01-10
Pages
253-5
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
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