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Putative 51,000-Mr protein marker for postsynaptic densities is virtually absent in cerebellum

Cerebrum and cerebellum contain numerous asymmetric synapses characterized by the presence of a postsynaptic thickening prominently stained by phosphotungstic acid and other electron-dense stains suitable for electron microscopy. A 51,000-Mr protein, copurified in postsynaptic density-enriched fract...

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Detalles Bibliográficos
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1982
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2112213/
https://www.ncbi.nlm.nih.gov/pubmed/7130281
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description Cerebrum and cerebellum contain numerous asymmetric synapses characterized by the presence of a postsynaptic thickening prominently stained by phosphotungstic acid and other electron-dense stains suitable for electron microscopy. A 51,000-Mr protein, copurified in postsynaptic density-enriched fractions from cerebrum, is considered to be a well established marker for the postsynaptic density. On the basis of two criteria, our studies demonstrate that the 51,000-Mr protein marker for postsynaptic densities is virtually absent in cerebellum, First, it is present in negligible amounts in deoxycholate-insoluble fractions from cerebellum but abundant in parallel fractions from cerebrum. Secondly, the 51,000-Mr protein, which binds 125I-calmodulin after SDS PAGE is readily visualized in membrane samples from cerebrum but is virtually undetectable in cerebellar samples. It is apparent that these results require reexamination of the role of the 51,000-Mr protein in postsynaptic density structures.
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spelling pubmed-21122132008-05-01 Putative 51,000-Mr protein marker for postsynaptic densities is virtually absent in cerebellum J Cell Biol Articles Cerebrum and cerebellum contain numerous asymmetric synapses characterized by the presence of a postsynaptic thickening prominently stained by phosphotungstic acid and other electron-dense stains suitable for electron microscopy. A 51,000-Mr protein, copurified in postsynaptic density-enriched fractions from cerebrum, is considered to be a well established marker for the postsynaptic density. On the basis of two criteria, our studies demonstrate that the 51,000-Mr protein marker for postsynaptic densities is virtually absent in cerebellum, First, it is present in negligible amounts in deoxycholate-insoluble fractions from cerebellum but abundant in parallel fractions from cerebrum. Secondly, the 51,000-Mr protein, which binds 125I-calmodulin after SDS PAGE is readily visualized in membrane samples from cerebrum but is virtually undetectable in cerebellar samples. It is apparent that these results require reexamination of the role of the 51,000-Mr protein in postsynaptic density structures. The Rockefeller University Press 1982-09-01 /pmc/articles/PMC2112213/ /pubmed/7130281 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
Putative 51,000-Mr protein marker for postsynaptic densities is virtually absent in cerebellum
title Putative 51,000-Mr protein marker for postsynaptic densities is virtually absent in cerebellum
title_full Putative 51,000-Mr protein marker for postsynaptic densities is virtually absent in cerebellum
title_fullStr Putative 51,000-Mr protein marker for postsynaptic densities is virtually absent in cerebellum
title_full_unstemmed Putative 51,000-Mr protein marker for postsynaptic densities is virtually absent in cerebellum
title_short Putative 51,000-Mr protein marker for postsynaptic densities is virtually absent in cerebellum
title_sort putative 51,000-mr protein marker for postsynaptic densities is virtually absent in cerebellum
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2112213/
https://www.ncbi.nlm.nih.gov/pubmed/7130281