Literature DB >> 6579538

Polymerization of actin: mechanism of the Mg2+-induced process at pH 8 and 20 degrees C.

C Frieden.   

Abstract

A detailed mechanism that fully accounts for the Mg2+-induced polymerization of actin in the presence or absence of Ca2+ at 20 degrees C and pH 8 is presented. In the absence of Ca2+, the mechanism of the Mg2+-induced polymerization is as follows: Mg2+ binds to a metal-binding site on G-actin and induces a conformational change, which is required for eventual polymerization. The overall dissociation constant for this binding is about 30 microM. This actin species then binds a second molecule of Mg2+ (Kd = 5 mM), which yields a species capable of polymerization. Dimer formation from this monomeric species is quite unfavorable, but trimer formation from dimer and monomer is much more favorable. The trimer may then elongate to give filaments. Ca2+, when present, binds at the same site as the tightly bound Mg2+ and must be displaced by Mg2+ before the conformational change can occur. The rate and dissociation constants for tight binding of Ca2+ and Mg2+ and for the conformational change are consistent with those observed previously by using a fluorescently labeled G-actin. With the mechanism proposed, it is possible to fit the full time course of polymerization over a wide range of actin concentrations, Mg2+ concentrations, and Ca2+ concentrations.

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Year:  1983        PMID: 6579538      PMCID: PMC390383          DOI: 10.1073/pnas.80.21.6513

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  17 in total

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Authors:  A Wegner; J Engel
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Journal:  J Biol Chem       Date:  1964-04       Impact factor: 5.157

3.  A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding.

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4.  The regulation of rabbit skeletal muscle contraction. I. Biochemical studies of the interaction of the tropomyosin-troponin complex with actin and the proteolytic fragments of myosin.

Authors:  J A Spudich; S Watt
Journal:  J Biol Chem       Date:  1971-08-10       Impact factor: 5.157

5.  Identification of a factor in conventional muscle actin preparations which inhibits actin filament self-association.

Authors:  S MacLean-Fletcher; T D Pollard
Journal:  Biochem Biophys Res Commun       Date:  1980-09-16       Impact factor: 3.575

6.  Effects of trace amounts of Ca2+ and Mg2+ on the polymerization of actin.

Authors:  K Maruyama
Journal:  Biochim Biophys Acta       Date:  1981-01-30

7.  The Mg2+-induced conformational change in rabbit skeletal muscle G-actin.

Authors:  C Frieden
Journal:  J Biol Chem       Date:  1982-03-25       Impact factor: 5.157

8.  Molecular recognition and the future of monoclonal antibodies.

Authors:  D Lane; H Koprowski
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9.  The first step in the polymerisation of actin.

Authors:  J F Rouayrenc; F Travers
Journal:  Eur J Biochem       Date:  1981-05

10.  A fluorescent probe for conformational changes in skeletal muscle G-actin.

Authors:  C Frieden; D Lieberman; H R Gilbert
Journal:  J Biol Chem       Date:  1980-10-10       Impact factor: 5.157

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  41 in total

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9.  Effects of lithium ions on actin polymerization in the presence of magnesium ions.

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10.  Formation and destabilization of actin filaments with tetramethylrhodamine-modified actin.

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