Literature DB >> 4226737

The distribution of protein-bound N-acetylneuraminic acid in subcellular fractions of rat brain.

E G Brunngraber, H Dekirmenjian, B D Brown.   

Abstract

Protein-bound N-acetylneuraminic acid and hexosamine, including the sialomucopolysaccharides, occur mainly in the least dense particles sedimented in the microsomal fraction from rat whole brain. Particles rich in protein-bound N-acetylneuraminic acid and hexosamine are also found in the subcellular fraction separated as a layer between 0.8m- and 1.2m-sucrose after centrifuging the crude mitochondrial preparation in a density gradient. This distribution is similar to that of the gangliosides and suggests an association of all of these substances in the same subcellular structures. It is postulated that the sialomucopolysaccharides, as well as the gangliosides, are components of cell membranes. Evidence is presented that indicates that there are quantitative differences between distribution of the gangliosides on the one hand, and protein-bound N-acetylneuraminic acid and hexosamine on the other. The ratio of protein-bound N-acetylneuraminic acid (and hexosamine) to gangliosidic N-acetylneuraminic acid (and hexosamine) present in individual subcellular fractions obtained by density-gradient centrifugation tends to increase with increasing particle density. Exposure of the crude mitochondrial fraction to osmotic ;shock' before density-gradient centrifugation causes a shift of the protein-bound N-acetylneuraminic acid and gangliosides to the less dense fractions. In some experiments, a selective shift of the protein-bound N-acetylneuraminic acid was observed.

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Year:  1967        PMID: 4226737      PMCID: PMC1270370          DOI: 10.1042/bj1030073

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  19 in total

1.  The thiobarbituric acid assay of sialic acids.

Authors:  L WARREN
Journal:  J Biol Chem       Date:  1959-08       Impact factor: 5.157

2.  Centrifugation of brain microsomes in a density gradient.

Authors:  V HANZON; G TOSCHI
Journal:  Exp Cell Res       Date:  1960-11       Impact factor: 3.905

3.  Electron microscopy of microsomal fractions from rat brain.

Authors:  V HANZON; G TOSCHI
Journal:  Exp Cell Res       Date:  1959-02       Impact factor: 3.905

4.  A biochemical study of brain microsomes.

Authors:  G TOSCHI
Journal:  Exp Cell Res       Date:  1959-02       Impact factor: 3.905

5.  Method for the determination of hexosamines in tissues.

Authors:  N F BOAS
Journal:  J Biol Chem       Date:  1953-10       Impact factor: 5.157

6.  The ground substance of the central nervous system revealed by histochemical staining.

Authors:  A HESS
Journal:  J Comp Neurol       Date:  1953-02       Impact factor: 3.215

7.  Inhibition of photophosphorylation and photosynthetic carbon cycle reactions by fatty acids and esters.

Authors:  T A Pedersen; M Kirk; J A Bassham
Journal:  Biochim Biophys Acta       Date:  1966-02-07

8.  Biosynthesis of glycoproteins of the Ehrlich ascites carcinoma cell membranes.

Authors:  G M Cook; M T Laico; E H Eylar
Journal:  Proc Natl Acad Sci U S A       Date:  1965-07       Impact factor: 11.205

9.  The pattern of mammalian brain gangliosides. II. Evaluation of the extraction procedures, postmortem changes and the effect of formalin preservation.

Authors:  K Suzuki
Journal:  J Neurochem       Date:  1965-07       Impact factor: 5.372

10.  Preparation and properties of sialomucopolysaccharides obtained from rat brain.

Authors:  E G Brunngraber; B D Brown
Journal:  Biochem J       Date:  1967-04       Impact factor: 3.857

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  12 in total

1.  On the action of ruthenium red and neuraminidase at the frog neuromuscular junction.

Authors:  B Robertson; K T Wann
Journal:  J Physiol       Date:  1987-01       Impact factor: 5.182

2.  Role of sialic acid in synaptosomal transport of amino acid transmitters.

Authors:  M M Zaleska; M Erecińska
Journal:  Proc Natl Acad Sci U S A       Date:  1987-03       Impact factor: 11.205

Review 3.  Biosynthesis of brain gangliosides.

Authors:  R Caputto; H J Maccioni; A Arce
Journal:  Mol Cell Biochem       Date:  1974-09-30       Impact factor: 3.396

4.  Free and protein-bound gangliosides in Triton X-100 extracts from rat brain.

Authors:  E G Brunngraber; V A Ziboh
Journal:  Lipids       Date:  1974-08       Impact factor: 1.880

5.  Distribution of gangliosides, glycoprotein-NANA and acetylcholinesterase in axonal and synaptosomal fractions of cat cerebellum.

Authors:  H Dekirmenjian; E G Brunngraber; N L Johnston; L M Larramendi
Journal:  Exp Brain Res       Date:  1969       Impact factor: 1.972

6.  Transmitter release: ruthenium red used to demonstrate a possible role of sialic acid containing substrates.

Authors:  G Baux; M Simonneau; L Tauc
Journal:  J Physiol       Date:  1979-06       Impact factor: 5.182

7.  The cerebral sodium-plus-potassium ion-stimulated adenosine triphosphatase of bovine brain and its microsomal matrix.

Authors:  I Pull; H MacIlwain
Journal:  Biochem J       Date:  1970-09       Impact factor: 3.857

8.  Blocking action of intracellularly injected neuraminidase on central synapses in vivo.

Authors:  F X Hipp; W Gielen; M A Davies; D H Hinzen
Journal:  Pflugers Arch       Date:  1980-05       Impact factor: 3.657

9.  The acid mucopolysaccharides of cattle retina.

Authors:  E R Berman; G Bach
Journal:  Biochem J       Date:  1968-06       Impact factor: 3.857

10.  Changes in glycoprotein carbohydrate content in the aging human brain.

Authors:  E G Brunngraber; J C Webster
Journal:  Neurochem Res       Date:  1986-04       Impact factor: 3.996

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