Literature DB >> 3597762

Facilitation of actin polymerization by interfilamentous factors.

E Cervén.   

Abstract

The polymerization of actin in low ionic strength buffer at 0 degrees C in the presence of 0.25 mM Mg2+ was studied by viscometry, turbidity and absorbance at 232 nm. Under these conditions, significant polymerization occurred only in the viscometer and not in isotropic mixtures. The polymerization rate with 0.25 mM MgCl2, as judged from shear viscosity, was equal to or greater than that observed with 0.1 M KCl and 0.25 mM MgCl2 at 0 degrees C, and was characterized by a longer nucleation period. Measurements of the turbidity at 350 nm (detecting filament formation and aggregation) and the absorbance at 232 nm (detecting conformational changes of the G-F transition) showed no evidence for polymerization or nucleation in a bulk solution at 0 degrees C when Mg2+ was added to 0.25 mM and, furthermore, F-actin nuclei were ineffective as seeds under these conditions. However, nucleation and polymerization by these criteria could be induced by raising the temperature to 20 degrees C. These results demonstrate the existence of narrow conditions when elongation of F-actin is dissociated from nucleation of oligomeric acceptor nuclei, even if monitored on the sub-molecular level (absorbance at 232 nm). Under these conditions, elongation appears to require anisotropic F-actin, i.e. that filaments are ordered by laminar flow.

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Year:  1987        PMID: 3597762     DOI: 10.1007/bf01767261

Source DB:  PubMed          Journal:  J Muscle Res Cell Motil        ISSN: 0142-4319            Impact factor:   2.698


  12 in total

1.  The measurement of actin concentration in solution: a comparison of methods.

Authors:  T W Houk; K Ue
Journal:  Anal Biochem       Date:  1974-11       Impact factor: 3.365

2.  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

3.  Capping one end of an actin filament affects elongation at the other end.

Authors:  K Maruyama; N Yamada; I Mabuchi
Journal:  J Biochem       Date:  1984-09       Impact factor: 3.387

4.  Organization of actin cytoskeleton in normal and regenerating arterial endothelial cells.

Authors:  G Gabbiani; F Gabbiani; D Lombardi; S M Schwartz
Journal:  Proc Natl Acad Sci U S A       Date:  1983-04       Impact factor: 11.205

5.  On the stability of cognitive processes.

Authors:  E Cervén
Journal:  Experientia       Date:  1985-06-15

6.  Sialyltransferase probing glycolytic energy metabolism in the plasma membrane.

Authors:  E Cervén; G Ronquist
Journal:  Naturwissenschaften       Date:  1985-02

7.  Nucleation of actin polymerization from profilactin. Opposite effects of different nuclei.

Authors:  F Markey; H Larsson; K Weber; U Lindberg
Journal:  Biochim Biophys Acta       Date:  1982-05-21

8.  Polymerization of G-actin by hydrodynamic shear stresses.

Authors:  J Borejdo; A Muhlrad; S J Leibovich; A Oplatka
Journal:  Biochim Biophys Acta       Date:  1981-01-30

9.  The cytomatrix: a short history of its study.

Authors:  K R Porter
Journal:  J Cell Biol       Date:  1984-07       Impact factor: 10.539

10.  Relation between cell activity and the distribution of cytoplasmic actin and myosin.

Authors:  I M Herman; N J Crisona; T D Pollard
Journal:  J Cell Biol       Date:  1981-07       Impact factor: 10.539

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  1 in total

1.  Cytoskeletal components enhance the autophosphorylation of retinal insulin receptor.

Authors:  Raju V S Rajala; Ammaji Rajala
Journal:  Chem Biol Interact       Date:  2009-03-31       Impact factor: 5.192

  1 in total

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