Literature DB >> 10319422

Polymerization of actin induced by a molar excess of ATP in a low salt buffer.

T Ikkai1, H Kondo.   

Abstract

The polymerization of actin induced by dilution has previously been reported, where a 1000-fold molar excess of ATP over actin resulted when actin was diluted to 4.0 micrograms/ml in low salt buffer A (0.1 mM ATP, 0.1 mM CaCl2, 2 mM Tris-HCl, pH 8.0, 5 mM 2-mercaptoethanol, 1 mM NaN3). Filaments formed by the addition of ATP to a 1000-fold molar excess over actin in buffer B (0.1 mM CaCl2, 2 mM Tris-HCl, pH 8.0, 1 mM NaN3) were then separated by gel-filtration. When ATP was removed from these filaments using Dowex-1, depolymerization occurred. Thus, the reversible polymerization induced by the dilution of actin or by addition of ATP can be ascribed to the binding of ATP at the low affinity site of actin.

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Year:  1999        PMID: 10319422     DOI: 10.1080/15216549900201753

Source DB:  PubMed          Journal:  Biochem Mol Biol Int        ISSN: 1039-9712


  1 in total

1.  Excimer fluorescence as a tool for monitoring protein domain dynamics applied to actin conformation changes based on circulary polarized fluorescence spectroscopy.

Authors:  T Ikkai; T Arii; K Shimada
Journal:  J Fluoresc       Date:  2006-05-13       Impact factor: 2.217

  1 in total

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