Literature DB >> 2050808

Mechanism of the insertion of actin monomers between the barbed ends of actin filaments and barbed end-bound insertin.

A Gaertner1, A Wegner.   

Abstract

Insertin, a protein purified from chicken gizzard smooth muscle, has been shown to retard but not to inhibit actin polymerization at the barbed ends of actin filaments. This effect has been explained by a model in which insertin remains bound to the barbed ends of actin filaments and new actin molecules are inserted into filaments between the barbed ends and barbed end-bound insertin molecules. In this paper we discuss the mechanism of the insertion reaction on a molecular level. A number of simple models were devised and were judged by their agreement with available experimental data. In one class of models insertin was assumed to dissociate from filament ends and to re-associate with the ends. Actin monomers would then bind to a filament end between a dissociation and an association reaction of insertin. In one of the two proposed models in this class insertin binds to an ATP-containing terminal subunit with higher affinity than to an ADP-containing terminal subunit. Dissociation of insertin is brought about by ATP hydrolysis at the terminal filament subunit. Insertion was then thought to re-associate with a filament end following binding of an ATP-containing actin monomer to the filament end. In the other of the two models' insertin was assumed to occur in two conformations which bind to filament ends with different affinities. Association and dissociation of insertin is caused by interconversion between the two forms of insertin. Both models turned out to be incompatible with experimental data. All types of models in which retardation of actin polymerization is brought about by dissociation and re-association of insertin with filament ends can be excluded by a common argument. As 10 nM insertin retards polymerization of 2 microns monomeric actin with maximal efficiency, the rate constant of binding of insertin to a filament end must be considerably higher (greater than 2 microM/10 nM = 200-fold). As the rate of association of actin with a barbed end is almost diffusion-controlled, assembly of insertin with a filament end would have to exceed the rate of a diffusion-controlled reaction. In the other class of models it was assumed that insertin remains permanently bound to filament ends during association or dissociation of an actin molecule and to move towards the terminal subunit of filaments. These models are compatible with experimental data. Thus, models are favoured where insertin remains bound to filament ends during polymerization and depolymerization of actin.

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Year:  1991        PMID: 2050808     DOI: 10.1007/bf01781171

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


  35 in total

1.  Head to tail polymerization of actin.

Authors:  A Wegner
Journal:  J Mol Biol       Date:  1976-11       Impact factor: 5.469

Review 2.  Probing nucleation, cutting and capping of actin filaments.

Authors:  A Gaertner; K Ruhnau; E Schröer; N Selve; M Wanger; A Wegner
Journal:  J Muscle Res Cell Motil       Date:  1989-02       Impact factor: 2.698

3.  Rate constants and equilibrium constants for binding of the gelsolin-actin complex to the barbed ends of actin filaments in the presence and absence of calcium.

Authors:  N Selve; A Wegner
Journal:  Eur J Biochem       Date:  1986-10-15

Review 4.  Bioenergetics and kinetics of microtubule and actin filament assembly-disassembly.

Authors:  T L Hill; M W Kirschner
Journal:  Int Rev Cytol       Date:  1982

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Authors:  M F Carlier; D Pantaloni; E D Korn
Journal:  J Biol Chem       Date:  1984-08-25       Impact factor: 5.157

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Authors:  M K Rees; M Young
Journal:  J Biol Chem       Date:  1967-10-10       Impact factor: 5.157

7.  Plasma actin depolymerizing factor has both calcium-dependent and calcium-independent effects on actin.

Authors:  H E Harris; A G Weeds
Journal:  Biochemistry       Date:  1983-05-24       Impact factor: 3.162

8.  7-Chloro-4-nitrobenzeno-2-oxa-1,3-diazole actin as a probe for actin polymerization.

Authors:  P Detmers; A Weber; M Elzinga; R E Stephens
Journal:  J Biol Chem       Date:  1981-01-10       Impact factor: 5.157

9.  A 45,000-mol-wt protein-actin complex from unfertilized sea urchin egg affects assembly properties of actin.

Authors:  H Hosoya; I Mabuchi
Journal:  J Cell Biol       Date:  1984-09       Impact factor: 10.539

10.  Rate constants for the reactions of ATP- and ADP-actin with the ends of actin filaments.

Authors:  T D Pollard
Journal:  J Cell Biol       Date:  1986-12       Impact factor: 10.539

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  5 in total

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Authors:  A Jahraus; M Egeberg; B Hinner; A Habermann; E Sackman; A Pralle; H Faulstich; V Rybin; H Defacque; G Griffiths
Journal:  Mol Biol Cell       Date:  2001-01       Impact factor: 4.138

Review 2.  Role of actin polymerization in cell locomotion: molecules and models.

Authors:  E L Bearer
Journal:  Am J Respir Cell Mol Biol       Date:  1993-06       Impact factor: 6.914

Review 3.  Focal adhesion as a signal transduction organelle.

Authors:  S H Lo; L B Chen
Journal:  Cancer Metastasis Rev       Date:  1994-03       Impact factor: 9.264

4.  Interactions of tensin with actin and identification of its three distinct actin-binding domains.

Authors:  S H Lo; P A Janmey; J H Hartwig; L B Chen
Journal:  J Cell Biol       Date:  1994-06       Impact factor: 10.539

5.  Tropomodulin caps the pointed ends of actin filaments.

Authors:  A Weber; C R Pennise; G G Babcock; V M Fowler
Journal:  J Cell Biol       Date:  1994-12       Impact factor: 10.539

  5 in total

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