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Membrane isolation on polylysine-coated beads. Plasma membrane from HeLa cells
HeLa cell plasma membranes have been purified after binding cells to polylysine-coated polyacrylamide beads. Cell attachment to beads and membrane recovery were maximal in a sucrose-acetate buffer, pH 5.0, at 25 degrees C. Measurements of ouabain-sensitive NaK-adenosine triphosphatase, membrane-boun...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1977
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2111560/ https://www.ncbi.nlm.nih.gov/pubmed/21192 |
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collection | PubMed |
description | HeLa cell plasma membranes have been purified after binding cells to polylysine-coated polyacrylamide beads. Cell attachment to beads and membrane recovery were maximal in a sucrose-acetate buffer, pH 5.0, at 25 degrees C. Measurements of ouabain-sensitive NaK-adenosine triphosphatase, membrane-bound 125I-wheat germ agglutinin, and chemical analyses showed that membranes on beads were of comparable or greater purity than membranes isolated by conventional methods. Because the isolation procedure is rapid (approximately 2.5 h), and produces membranes whose protoplasmic surfaces are fully exposed, it should be a useful supplement to standard isolation techniques. |
format | Text |
id | pubmed-2111560 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1977 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21115602008-05-01 Membrane isolation on polylysine-coated beads. Plasma membrane from HeLa cells J Cell Biol Articles HeLa cell plasma membranes have been purified after binding cells to polylysine-coated polyacrylamide beads. Cell attachment to beads and membrane recovery were maximal in a sucrose-acetate buffer, pH 5.0, at 25 degrees C. Measurements of ouabain-sensitive NaK-adenosine triphosphatase, membrane-bound 125I-wheat germ agglutinin, and chemical analyses showed that membranes on beads were of comparable or greater purity than membranes isolated by conventional methods. Because the isolation procedure is rapid (approximately 2.5 h), and produces membranes whose protoplasmic surfaces are fully exposed, it should be a useful supplement to standard isolation techniques. The Rockefeller University Press 1977-10-01 /pmc/articles/PMC2111560/ /pubmed/21192 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Articles Membrane isolation on polylysine-coated beads. Plasma membrane from HeLa cells |
title | Membrane isolation on polylysine-coated beads. Plasma membrane from HeLa cells |
title_full | Membrane isolation on polylysine-coated beads. Plasma membrane from HeLa cells |
title_fullStr | Membrane isolation on polylysine-coated beads. Plasma membrane from HeLa cells |
title_full_unstemmed | Membrane isolation on polylysine-coated beads. Plasma membrane from HeLa cells |
title_short | Membrane isolation on polylysine-coated beads. Plasma membrane from HeLa cells |
title_sort | membrane isolation on polylysine-coated beads. plasma membrane from hela cells |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2111560/ https://www.ncbi.nlm.nih.gov/pubmed/21192 |