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MITOCHONDRIAL AUTONOMY : Sialic Acid Residues on the Surface of Isolated Rat Cerebral Cortex and Liver Mitochondria

N-acetylneuraminic acid at the surfaces of rat cerebral cortex and liver mitochondria and derived mitoplasts (inner membrane plus matrix particles) was studied biochemically and electrokinetically. Rat cerebral cortex mitochondria in 0.0145 M NaCl, 4.5% sorbitol, pH 7.2 ± 0.1, 0.6 mM NaHCO(3), had a...

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Detalles Bibliográficos
Autores principales: Bosmann, H. Bruce, Myers, Marjorie W., Dehond, Delena, Ball, Richard, Case, Kenneth R.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1972
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2108747/
https://www.ncbi.nlm.nih.gov/pubmed/4653414
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author Bosmann, H. Bruce
Myers, Marjorie W.
Dehond, Delena
Ball, Richard
Case, Kenneth R.
author_facet Bosmann, H. Bruce
Myers, Marjorie W.
Dehond, Delena
Ball, Richard
Case, Kenneth R.
author_sort Bosmann, H. Bruce
collection PubMed
description N-acetylneuraminic acid at the surfaces of rat cerebral cortex and liver mitochondria and derived mitoplasts (inner membrane plus matrix particles) was studied biochemically and electrokinetically. Rat cerebral cortex mitochondria in 0.0145 M NaCl, 4.5% sorbitol, pH 7.2 ± 0.1, 0.6 mM NaHCO(3), had an electrophoretic mobility of - 2.88 ± 0.01 µ/sec per v per cm. In the same solution the electrophoretic mobility of rat liver mitochondria was - 2.01 ± 0.02, of rat liver mitoplasts was - 1.22 ± 0.07, and of rat cerebral cortex mitoplasts - 0.91 ± 0.04 µ/sec per v per cm. Treatment of these particles with 50 µg neuraminidase/mg particle protein resulted in the following electrophoretic mobilities in µ/sec per v per cm: rat cerebral cortex mitochondria, - 2.27; rat liver mitochondria, - 1.40; rat cerebral cortex mitoplasts, - 0.78; and rat liver mitoplasts, - 1.10. Rat liver mitochondria, mitoplasts, and outer mitochondrial membranes contained 2.0, 1.1, and 4.1 nmoles of sialic acid/mg protein, respectively. 10% of the liver mitochondrial protein and 27.5% of the sialic acid was solubilized in the mitoplast and outer membrane isolation procedure. Rat cerebral cortex mitochondria, mitoplasts, and outer mitochondrial membranes contained 3.1, 0.8, and 6.2 nmoles sialic acid/mg protein, respectively; 10% of the brain mitochondrial protein and 49 % of the sialic acid was solubilized in the mitoplast and outer membrane isolation solution procedure. Treatment of both the rat liver and cerebral cortex mitochondria with 50 µg neuraminidase (dry weight) /mg protein resulted in the release of about 50% of the available outer membrane sialic acid residues. Treatment of all of the particles with trypsin caused release of sialic acid but did not greatly affect the particle electrophoretic mobility. In each instance, curves of pH vs. electrophoretic mobility indicated that the particle surface contained an acid dissociable group, most likely a carboxyl group of sialic acid with pK(a) ∼ 2.7. Treatment of either the rat liver or the cerebral cortex mitochondria with trypsinized concanavalin A did not affect the particle electrophoretic mobility but did cause a decrease in the electrophoretic mobility of L5178Y mouse leukemic cells.
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spelling pubmed-21087472008-05-01 MITOCHONDRIAL AUTONOMY : Sialic Acid Residues on the Surface of Isolated Rat Cerebral Cortex and Liver Mitochondria Bosmann, H. Bruce Myers, Marjorie W. Dehond, Delena Ball, Richard Case, Kenneth R. J Cell Biol Article N-acetylneuraminic acid at the surfaces of rat cerebral cortex and liver mitochondria and derived mitoplasts (inner membrane plus matrix particles) was studied biochemically and electrokinetically. Rat cerebral cortex mitochondria in 0.0145 M NaCl, 4.5% sorbitol, pH 7.2 ± 0.1, 0.6 mM NaHCO(3), had an electrophoretic mobility of - 2.88 ± 0.01 µ/sec per v per cm. In the same solution the electrophoretic mobility of rat liver mitochondria was - 2.01 ± 0.02, of rat liver mitoplasts was - 1.22 ± 0.07, and of rat cerebral cortex mitoplasts - 0.91 ± 0.04 µ/sec per v per cm. Treatment of these particles with 50 µg neuraminidase/mg particle protein resulted in the following electrophoretic mobilities in µ/sec per v per cm: rat cerebral cortex mitochondria, - 2.27; rat liver mitochondria, - 1.40; rat cerebral cortex mitoplasts, - 0.78; and rat liver mitoplasts, - 1.10. Rat liver mitochondria, mitoplasts, and outer mitochondrial membranes contained 2.0, 1.1, and 4.1 nmoles of sialic acid/mg protein, respectively. 10% of the liver mitochondrial protein and 27.5% of the sialic acid was solubilized in the mitoplast and outer membrane isolation procedure. Rat cerebral cortex mitochondria, mitoplasts, and outer mitochondrial membranes contained 3.1, 0.8, and 6.2 nmoles sialic acid/mg protein, respectively; 10% of the brain mitochondrial protein and 49 % of the sialic acid was solubilized in the mitoplast and outer membrane isolation solution procedure. Treatment of both the rat liver and cerebral cortex mitochondria with 50 µg neuraminidase (dry weight) /mg protein resulted in the release of about 50% of the available outer membrane sialic acid residues. Treatment of all of the particles with trypsin caused release of sialic acid but did not greatly affect the particle electrophoretic mobility. In each instance, curves of pH vs. electrophoretic mobility indicated that the particle surface contained an acid dissociable group, most likely a carboxyl group of sialic acid with pK(a) ∼ 2.7. Treatment of either the rat liver or the cerebral cortex mitochondria with trypsinized concanavalin A did not affect the particle electrophoretic mobility but did cause a decrease in the electrophoretic mobility of L5178Y mouse leukemic cells. The Rockefeller University Press 1972-10-01 /pmc/articles/PMC2108747/ /pubmed/4653414 Text en Copyright © 1972 by The Rockefeller University Press 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 Article
Bosmann, H. Bruce
Myers, Marjorie W.
Dehond, Delena
Ball, Richard
Case, Kenneth R.
MITOCHONDRIAL AUTONOMY : Sialic Acid Residues on the Surface of Isolated Rat Cerebral Cortex and Liver Mitochondria
title MITOCHONDRIAL AUTONOMY : Sialic Acid Residues on the Surface of Isolated Rat Cerebral Cortex and Liver Mitochondria
title_full MITOCHONDRIAL AUTONOMY : Sialic Acid Residues on the Surface of Isolated Rat Cerebral Cortex and Liver Mitochondria
title_fullStr MITOCHONDRIAL AUTONOMY : Sialic Acid Residues on the Surface of Isolated Rat Cerebral Cortex and Liver Mitochondria
title_full_unstemmed MITOCHONDRIAL AUTONOMY : Sialic Acid Residues on the Surface of Isolated Rat Cerebral Cortex and Liver Mitochondria
title_short MITOCHONDRIAL AUTONOMY : Sialic Acid Residues on the Surface of Isolated Rat Cerebral Cortex and Liver Mitochondria
title_sort mitochondrial autonomy : sialic acid residues on the surface of isolated rat cerebral cortex and liver mitochondria
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2108747/
https://www.ncbi.nlm.nih.gov/pubmed/4653414
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