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Isolation of acetylcholine receptor clusters in substrate-associated material from cultured rat myotubes using saponin

After exposure of rat myotube cultures to saponin, less than 1% of the cellular protein was found to remain associated with the tissue culture substrate. This substrate-associated material contained approximately 10% of the acetylcholine receptors (AChRs) and greater than 80% of the large, ventral A...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1984
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2113409/
https://www.ncbi.nlm.nih.gov/pubmed/6381511
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description After exposure of rat myotube cultures to saponin, less than 1% of the cellular protein was found to remain associated with the tissue culture substrate. This substrate-associated material contained approximately 10% of the acetylcholine receptors (AChRs) and greater than 80% of the large, ventral AChR clusters present in the original culture. The domain structure evident in intact cells was maintained in AChR clusters after isolation using saponin. However, vinculin, present at the clusters of intact cells, was absent from isolated clusters. Dodecyl sulfate PAGE showed that substrate-associated material enriched in AChR clusters contained a distinctive set of polypeptides, the major ones electrophoresing with apparent molecular weights of 43,000 and 49,000. Saponin extraction of cultures of established cell lines also yielded substrate-associated material with characteristics particular to the cell type.
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spelling pubmed-21134092008-05-01 Isolation of acetylcholine receptor clusters in substrate-associated material from cultured rat myotubes using saponin J Cell Biol Articles After exposure of rat myotube cultures to saponin, less than 1% of the cellular protein was found to remain associated with the tissue culture substrate. This substrate-associated material contained approximately 10% of the acetylcholine receptors (AChRs) and greater than 80% of the large, ventral AChR clusters present in the original culture. The domain structure evident in intact cells was maintained in AChR clusters after isolation using saponin. However, vinculin, present at the clusters of intact cells, was absent from isolated clusters. Dodecyl sulfate PAGE showed that substrate-associated material enriched in AChR clusters contained a distinctive set of polypeptides, the major ones electrophoresing with apparent molecular weights of 43,000 and 49,000. Saponin extraction of cultures of established cell lines also yielded substrate-associated material with characteristics particular to the cell type. The Rockefeller University Press 1984-09-01 /pmc/articles/PMC2113409/ /pubmed/6381511 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
Isolation of acetylcholine receptor clusters in substrate-associated material from cultured rat myotubes using saponin
title Isolation of acetylcholine receptor clusters in substrate-associated material from cultured rat myotubes using saponin
title_full Isolation of acetylcholine receptor clusters in substrate-associated material from cultured rat myotubes using saponin
title_fullStr Isolation of acetylcholine receptor clusters in substrate-associated material from cultured rat myotubes using saponin
title_full_unstemmed Isolation of acetylcholine receptor clusters in substrate-associated material from cultured rat myotubes using saponin
title_short Isolation of acetylcholine receptor clusters in substrate-associated material from cultured rat myotubes using saponin
title_sort isolation of acetylcholine receptor clusters in substrate-associated material from cultured rat myotubes using saponin
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2113409/
https://www.ncbi.nlm.nih.gov/pubmed/6381511