Literature DB >> 10524632

Reconstitution of actin-based motility of Listeria and Shigella using pure proteins.

T P Loisel1, R Boujemaa, D Pantaloni, M F Carlier.   

Abstract

Actin polymerization is essential for cell locomotion and is thought to generate the force responsible for cellular protrusions. The Arp2/3 complex is required to stimulate actin assembly at the leading edge in response to signalling. The bacteria Listeria and Shigella bypass the signalling pathway and harness the Arp2/3 complex to induce actin assembly and to propel themselves in living cells. However, the Arp2/3 complex alone is insufficient to promote movement. Here we have used pure components of the actin cytoskeleton to reconstitute sustained movement in Listeria and Shigella in vitro. Actin-based propulsion is driven by the free energy released by ATP hydrolysis linked to actin polymerization, and does not require myosin. In addition to actin and activated Arp2/3 complex, actin depolymerizing factor (ADF, or cofilin) and capping protein are also required for motility as they maintain a high steady-state level of G-actin, which controls the rate of unidirectional growth of actin filaments at the surface of the bacterium. The movement is more effective when profilin, alpha-actinin and VASP (for Listeria) are also included. These results have implications for our understanding of the mechanism of actin-based motility in cells.

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Year:  1999        PMID: 10524632     DOI: 10.1038/44183

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  342 in total

1.  Feedback interactions between cell-cell adherens junctions and cytoskeletal dynamics in newt lung epithelial cells.

Authors:  C M Waterman-Storer; W C Salmon; E D Salmon
Journal:  Mol Biol Cell       Date:  2000-07       Impact factor: 4.138

Review 2.  Actin-based motility of intracellular microbial pathogens.

Authors:  M B Goldberg
Journal:  Microbiol Mol Biol Rev       Date:  2001-12       Impact factor: 11.056

3.  Cryptosporidium parvum infection requires host cell actin polymerization.

Authors:  D A Elliott; D J Coleman; M A Lane; R C May; L M Machesky; D P Clark
Journal:  Infect Immun       Date:  2001-09       Impact factor: 3.441

Review 4.  Molecular basis of the intracellular spreading of Shigella.

Authors:  T Suzuki; C Sasakawa
Journal:  Infect Immun       Date:  2001-10       Impact factor: 3.441

5.  Actin pedestal formation by enteropathogenic Escherichia coli and intracellular motility of Shigella flexneri are abolished in N-WASP-defective cells.

Authors:  S Lommel; S Benesch; K Rottner; T Franz; J Wehland; R Kühn
Journal:  EMBO Rep       Date:  2001-09       Impact factor: 8.807

Review 6.  Actin and pollen tube growth.

Authors:  L Vidali; P K Hepler
Journal:  Protoplasma       Date:  2001       Impact factor: 3.356

7.  Growth of branched actin networks against obstacles.

Authors:  A E Carlsson
Journal:  Biophys J       Date:  2001-10       Impact factor: 4.033

8.  Actin polymerization is essential for pollen tube growth.

Authors:  L Vidali; S T McKenna; P K Hepler
Journal:  Mol Biol Cell       Date:  2001-08       Impact factor: 4.138

9.  A WASp-VASP complex regulates actin polymerization at the plasma membrane.

Authors:  F Castellano; C Le Clainche; D Patin; M F Carlier; P Chavrier
Journal:  EMBO J       Date:  2001-10-15       Impact factor: 11.598

10.  Crystal structure of CapZ: structural basis for actin filament barbed end capping.

Authors:  Atsuko Yamashita; Kayo Maeda; Yuichiro Maéda
Journal:  EMBO J       Date:  2003-04-01       Impact factor: 11.598

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