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PMID: 129341 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Matrix vesicles of bovine fetal cartilage: metabolic potential and solubilization with detergents.

Federation proceedings ·Vol. 35 ·No. 2 ·1976-02-00 ·Pages 154-5

Sajdera SW, Franklin S, Fortuna R

Abstract

The ATPase of matrix vesicles is not stimulated by calcium ions, nor do the vesicles have any capacity to metabolize glucose. ADPase of high activity is also present; thus vesicles cannot be a component of the conventional ATP cycle, in which energy is stored by phosphorylating ADP and released by hydrolyzing the resultant ATP. These results do not support speculations that matrix vesicles might function by concentrating calcium via an energy-dependent ion transport system such as those found in the plasma membrane and the sarcoplasmic reticulum. Matrix vesicles' alkaline phosphatase can be solubilized by treatment with certain detergents: sodium dodecyl sulfate (12 mM and 16 mM), cetylpyridinium chloride (14mM), and deoxycholic acid (DOC, 14 MM). The first two detergents denature the enzyme during storage whereas DOC does not. DOC will also solubilize ATPase and inorganic pyrophosphatase. Yields of the three enzymes are 85-95%. Dialysis of a DOC digest of vesicles removes DOC and 43% of protein, and also causes much of the alkaline phosphatase to become particulate once again.

MeSH Terms
Adenosine Triphosphatases/metabolism Alkaline Phosphatase/metabolism Animals Cartilage/embryology,enzymology,metabolism Cattle Cell Fractionation Cetylpyridinium Deoxycholic Acid Detergents Epiphyses Glucose/metabolism Sodium Dodecyl Sulfate Solubility
Chemicals
Detergents Deoxycholic Acid Sodium Dodecyl Sulfate Cetylpyridinium Alkaline Phosphatase Adenosine Triphosphatases Glucose
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Sajdera S W
Franklin S
Fortuna R
Article Info
Journal
Federation proceedings
Abbr.
Fed Proc
ISSN
0014-9446
Published
1976-02-00
Pages
154-5
Language
English
Region
United States
NLM ID
0372771
Subset
IM
External Links
PubMed source
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