Literature DB >> 6682116

Direct electron microscopic visualization of barbed end capping and filament cutting by intestinal microvillar 95-kdalton protein (villin): a new actin assembly assay using the Limulus acrosomal process.

E M Bonder, M S Mooseker.   

Abstract

We have re-examined the Ca(++)-dependent interaction of an intestinal microvillar 95- kdalton protein (MV-95K) and actin using the isolated acrosomal process bundles from limulus sperm. Making use of the processes as nuclei for assembling actin filaments, we quantitatively and qualitatively examined MV-95K's effect on filament assembly and on F- actin, both in the presence and in the absence of Ca(++). The acrosomal processes are particularly advantageous for this approach because they nucleate large numbers of filaments, they are extremely stable, and their morphology can be used to determine the polarity of any nucleated filaments. When filament nucleation was initiated in the presence of MV-95K and the absence of Ca(++), there was biased filament assembly from the bundle ends. The calculated elongation rates from both the barbed and pointed filament ends were virtually indistinguishable from control preparations. In the presence of Ca(++), MV-95K completely inhibited filament assembly from the barbed filament end without affecting the initial rate of assembly from the pointed filament end. The inhibition of assembly results from MV-95K binding to and capping the barbed filament end, thereby preventing monomer addition. This indicates that, while MV-95K is a potent nucleator of actin assembly, it is also a potent inhibitor of actin filament elongation. To examine the effects of MV-95K on F-actin in the presence of Ca(++), we developed an assay where MV-95K is added to filaments previously assembled from acrosomal processes without causing filament breakage during mixing. These results clearly demonstrated that rapid filament shortening by MV-95K results through a mechanism of disrupting intrafilament monomer-monomer interactions. Finally, we show that tropomyosin-containing actin filaments are insensitive to cutting, but not to capping, by MV-95K in the presence of Ca(++).

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Year:  1983        PMID: 6682116      PMCID: PMC2112331          DOI: 10.1083/jcb.96.4.1097

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


  38 in total

1.  Head to tail polymerization of actin.

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

2.  Polymerization polarity of actin.

Authors:  T Hayashi; W Ip
Journal:  J Mechanochem Cell Motil       Date:  1976-03

3.  Troponin-tropomyosin complex. Column chromatographic separation and activity of the three, active troponin components with and without tropomyosin present.

Authors:  E Eisenberg; W W Kielley
Journal:  J Biol Chem       Date:  1974-08-10       Impact factor: 5.157

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.  Cleavage of structural proteins during the assembly of the head of bacteriophage T4.

Authors:  U K Laemmli
Journal:  Nature       Date:  1970-08-15       Impact factor: 49.962

6.  Uni-directional growth of F-actin.

Authors:  H Kondo; S Ishiwata
Journal:  J Biochem       Date:  1976-01       Impact factor: 3.387

7.  SDS microslab linear gradient polyacrylamide gel electrophoresis.

Authors:  P T Matsudaira; D R Burgess
Journal:  Anal Biochem       Date:  1978-07-01       Impact factor: 3.365

8.  Evidence for biased bidirectional polymerization of actin filaments using heavy meromyosin prepared by an improved method.

Authors:  D T Woodrum; S A Rich; T D Pollard
Journal:  J Cell Biol       Date:  1975-10       Impact factor: 10.539

9.  Actin filaments in the acrosomal reaction of Limulus sperm. Motion generated by alterations in the packing of the filaments.

Authors:  L G Tilney
Journal:  J Cell Biol       Date:  1975-02       Impact factor: 10.539

10.  Nucleation of polar actin filament assembly by a positively charged surface.

Authors:  S S Brown; J A Spudich
Journal:  J Cell Biol       Date:  1979-02       Impact factor: 10.539

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  27 in total

Review 1.  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

Review 2.  Actin-based organelle movement.

Authors:  V R Simon; L A Pon
Journal:  Experientia       Date:  1996-12-15

3.  The effects of a 45 000 molecular weight protein from unfertilized sea urchin eggs and its 1:1 actin complex on actin filaments.

Authors:  L M Coluccio; P A Sedlar; J Bryan
Journal:  J Muscle Res Cell Motil       Date:  1986-04       Impact factor: 2.698

4.  Kinetic analysis of F-actin depolymerization in the presence of platelet gelsolin and gelsolin-actin complexes.

Authors:  J Bryan; L M Coluccio
Journal:  J Cell Biol       Date:  1985-10       Impact factor: 10.539

5.  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

6.  How Listeria exploits host cell actin to form its own cytoskeleton. II. Nucleation, actin filament polarity, filament assembly, and evidence for a pointed end capper.

Authors:  L G Tilney; D J DeRosier; A Weber; M S Tilney
Journal:  J Cell Biol       Date:  1992-07       Impact factor: 10.539

7.  Mechanism of regulation of actin polymerization by Physarum profilin.

Authors:  K Ozaki; S Hatano
Journal:  J Cell Biol       Date:  1984-06       Impact factor: 10.539

8.  Organization of the actin filament cytoskeleton in the intestinal brush border: a quantitative and qualitative immunoelectron microscope study.

Authors:  D Drenckhahn; R Dermietzel
Journal:  J Cell Biol       Date:  1988-09       Impact factor: 10.539

9.  Cytochalasin B slows but does not prevent monomer addition at the barbed end of the actin filament.

Authors:  E M Bonder; M S Mooseker
Journal:  J Cell Biol       Date:  1986-01       Impact factor: 10.539

10.  Inhibition of actin filament depolymerization by the Dictyostelium 30,000-D actin-bundling protein.

Authors:  S H Zigmond; R Furukawa; M Fechheimer
Journal:  J Cell Biol       Date:  1992-11       Impact factor: 10.539

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