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Localization of Z-protein in isolated Z-disk sheets of chicken leg muscle

Immunoblotting studies with antisera against Z-protein, desmin, and alpha-actinin showed that Z-protein is clearly distinguishable from desmin and alpha-actinin. Z-protein is not a proteolytic product of another protein but is an intrinsic component of chicken breast muscle myofibrils. In these expe...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1982
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2112373/
https://www.ncbi.nlm.nih.gov/pubmed/6754746
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description Immunoblotting studies with antisera against Z-protein, desmin, and alpha-actinin showed that Z-protein is clearly distinguishable from desmin and alpha-actinin. Z-protein is not a proteolytic product of another protein but is an intrinsic component of chicken breast muscle myofibrils. In these experiments, an SDS extract of intact muscle was first electrophoresed in a polyacrylamide gel, and then proteins were transferred to a nitrocellulose paper sheet. Detection of each protein on the sheet was made possible by the application of the indirect immunofluorescence technique with the respective antiserum. Immunofluorescence microscope studies using these antisera revealed that Z-protein has the same distribution as alpha-actinin in isolated Z- disk sheets. Anti-Z-protein antiserum and anti-alpha-actinin antiserum stained the interior of Z-disks. On the other hand, antiserum against desmin stained the periphery of Z-disks in isolated Z-disk sheets.
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spelling pubmed-21123732008-05-01 Localization of Z-protein in isolated Z-disk sheets of chicken leg muscle J Cell Biol Articles Immunoblotting studies with antisera against Z-protein, desmin, and alpha-actinin showed that Z-protein is clearly distinguishable from desmin and alpha-actinin. Z-protein is not a proteolytic product of another protein but is an intrinsic component of chicken breast muscle myofibrils. In these experiments, an SDS extract of intact muscle was first electrophoresed in a polyacrylamide gel, and then proteins were transferred to a nitrocellulose paper sheet. Detection of each protein on the sheet was made possible by the application of the indirect immunofluorescence technique with the respective antiserum. Immunofluorescence microscope studies using these antisera revealed that Z-protein has the same distribution as alpha-actinin in isolated Z- disk sheets. Anti-Z-protein antiserum and anti-alpha-actinin antiserum stained the interior of Z-disks. On the other hand, antiserum against desmin stained the periphery of Z-disks in isolated Z-disk sheets. The Rockefeller University Press 1982-10-01 /pmc/articles/PMC2112373/ /pubmed/6754746 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
Localization of Z-protein in isolated Z-disk sheets of chicken leg muscle
title Localization of Z-protein in isolated Z-disk sheets of chicken leg muscle
title_full Localization of Z-protein in isolated Z-disk sheets of chicken leg muscle
title_fullStr Localization of Z-protein in isolated Z-disk sheets of chicken leg muscle
title_full_unstemmed Localization of Z-protein in isolated Z-disk sheets of chicken leg muscle
title_short Localization of Z-protein in isolated Z-disk sheets of chicken leg muscle
title_sort localization of z-protein in isolated z-disk sheets of chicken leg muscle
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2112373/
https://www.ncbi.nlm.nih.gov/pubmed/6754746