Literature DB >> 156729

Chick brain actin and myosin. Isolation and characterization.

E R Kuczmarski, J L Rosenbaum.   

Abstract

Brain actin extracted from an acetone powder of chick brains was purified by a cycle of polymerization-depolymerization followed by molecular sieve chromatography. The brain actin had a subunit molecular weight of 42,000 daltons as determined by co-electrophoresis with muscle actin. It underwent salt-dependent g to f transformation to form double helical actin filaments which could be "decorated" by muscle myosin subfragment 1. A critical concentration for polymerization of 1.3 microM was determined by measuring either the change in viscosity or absorbance at 232 nm. Brain actin was also capable of stimulating the ATPase activity of muscle myosin. Brain myosin was isolated from whole chick brain by a procedure involving high salt extraction, ammonium sulfate fractionation and molecular sieve chromatography. The purified myosin was composed of a 200,000-dalton heavy chain and three lower molecular weight light chains. In 0.6 M KCl the brain myosin had ATPase activity which was inhibited by Mg++, stimulated by Ca++, and maximally activated by EDTA. When dialyzed against 0.1 M KCl, the brain myosin self-assembled into short bipolar filaments. The bipolar filaments associated with each other to form long concatamers, and this association was enhanced by high concentrations of Mg++ ion. The brain myosin did not interact with chicken skeletal muscle myosin to form hybrid filaments. Furthermore, antibody recognition studies demonstrated that myosins from chicken brain, skeletal muscle, and smooth muscle were unique.

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Year:  1979        PMID: 156729      PMCID: PMC2110348          DOI: 10.1083/jcb.80.2.341

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  11 in total

1.  The G-F equilibrium in actin solutions under various conditions.

Authors:  M KASAI; S ASAKURA; F OOSAWA
Journal:  Biochim Biophys Acta       Date:  1962-02-12

2.  Polymerization of Acanthamoeba actin. Kinetics, thermodynamics, and co-polymerization with muscle actin.

Authors:  D J Gordon; Y Z Yang; E D Korn
Journal:  J Biol Chem       Date:  1976-12-10       Impact factor: 5.157

3.  The adenosine triphosphatase activity of acto-heavy meromyosin. A kinetic analysis of actin activation.

Authors:  E Eisenberg; C Moos
Journal:  Biochemistry       Date:  1968-04       Impact factor: 3.162

4.  Substructure of the myosin molecule. IV. Interactions of myosin and its subfragments with adenosine triphosphate and F-actin.

Authors:  S S Margossian; S Lowey
Journal:  J Mol Biol       Date:  1973-03-05       Impact factor: 5.469

5.  Actin in growing nerve cells.

Authors:  R E Fine; D Bray
Journal:  Nat New Biol       Date:  1971-11-24

6.  Conformational changes associated with polymerization and nucleotide binding in actin molecules.

Authors:  S Higashi; F Oosawa
Journal:  J Mol Biol       Date:  1965-07       Impact factor: 5.469

7.  Purification and characterization of myosin from the clonal rat glial cell strain C-6.

Authors:  J F Ash
Journal:  J Biol Chem       Date:  1975-05-10       Impact factor: 5.157

8.  Isolation and polymerization of brain actin.

Authors:  S Moring; M Ruscha; P Cooke; F Samson
Journal:  J Neurobiol       Date:  1975-03

9.  The contractile basis of ameboid movement. II. Structure and contractility of motile extracts and plasmalemma-ectoplasm ghosts.

Authors:  D L Taylor; J A Rhodes; S A Hammond
Journal:  J Cell Biol       Date:  1976-07       Impact factor: 10.539

10.  The localization of actin-like fibers in cultured neuroblastoma cells as revealed by heavy meromyosin binding.

Authors:  C M Chang; R D Goldman
Journal:  J Cell Biol       Date:  1973-06       Impact factor: 10.539

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  13 in total

Review 1.  Molecular motors in axonal transport. Cellular and molecular biology of kinesin.

Authors:  J L Cyr; S T Brady
Journal:  Mol Neurobiol       Date:  1992 Summer-Fall       Impact factor: 5.590

2.  Expression of actin and myosin genes during PC12 cell differentiation.

Authors:  R C Henke; O Tolhurst; J W Sentry; P Gunning; P L Jeffrey
Journal:  Neurochem Res       Date:  1991-06       Impact factor: 3.996

3.  Myosin from pancreatic acinar carcinoma cells. Isolation, characterization and demonstration of heavy- and light-chain phosphorylation.

Authors:  T K Watanabe; E R Kuczmarski; J K Reddy
Journal:  Biochem J       Date:  1987-11-01       Impact factor: 3.857

4.  Physical and enzymatic properties of myosin from porcine brain.

Authors:  D S Hobbs; D W Frederiksen
Journal:  Biophys J       Date:  1980-11       Impact factor: 4.033

5.  Activation of myosin ATPase by actin isolated from cultured BHK cells and the effect of gelsolin.

Authors:  A Koffer; J Sleep
Journal:  J Muscle Res Cell Motil       Date:  1987-12       Impact factor: 2.698

6.  The relationship between stress fiber-like structures and nascent myofibrils in cultured cardiac myocytes.

Authors:  A A Dlugosz; P B Antin; V T Nachmias; H Holtzer
Journal:  J Cell Biol       Date:  1984-12       Impact factor: 10.539

7.  Identification of recombinant phages containing sequences from different rat myosin heavy chain genes.

Authors:  U Nudel; D Katcoff; Y Carmon; D Zevin-Sonkin; Z Levi; Y Shaul; M Shani; D Yaffe
Journal:  Nucleic Acids Res       Date:  1980-05-24       Impact factor: 16.971

8.  Purification, characterization and substrate specificity of calmodulin-dependent myosin light-chain kinase from bovine brain.

Authors:  D C Bartelt; S Moroney; D J Wolff
Journal:  Biochem J       Date:  1987-11-01       Impact factor: 3.857

9.  Actin from pig and rat uterus.

Authors:  J S Elce; A S Elbrecht; M U Middlestadt; E J McIntyre; P J Anderson
Journal:  Biochem J       Date:  1981-03-01       Impact factor: 3.857

10.  Phosphorylation and actin activation of brain myosin.

Authors:  B Barylko; A Sobieszek
Journal:  EMBO J       Date:  1983       Impact factor: 11.598

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