The state of the filament
Open Access
- 1 March 2005
- journal article
- review article
- Published by Springer Nature in EMBO Reports
- Vol. 6 (3) , 220-226
- https://doi.org/10.1038/sj.embor.7400363
Abstract
Movement is a defining characteristic of life. Macroscopic motion is driven by the dynamic interactions of myosin with actin filaments in muscle. Directed polymerization of actin behind the advancing membrane of a eukaryotic cell generates microscopic movement. Despite the fundamental importance of actin in these processes, the structure of the actin filament remains unknown. The Holmes model of the actin filament was published 15 years ago, and although it has been widely accepted, no high‐resolution structural data have yet confirmed its veracity. Here, we review the implications of recently determined structures of F‐actin‐binding proteins for the structure of the actin filament and suggest a series of in silico tests for actin‐filament models. We also review the significance of these structures for the arp2/3‐mediated branched filament.Keywords
This publication has 30 references indexed in Scilit:
- Structural basis of actin filament nucleation and processive capping by a formin homology 2 domainNature, 2005
- Crystal structures of the vitamin D-binding protein and its complex with actin: Structural basis of the actin-scavenger systemProceedings of the National Academy of Sciences, 2002
- Polylysine Induces an Antiparallel Actin Dimer That Nucleates Filament AssemblyPublished by Elsevier ,2002
- Control of Actin Dynamics by Proteins Made of β-Thymosin RepeatsJournal of Biological Chemistry, 2002
- Hydrolysis of ATP by Polymerized Actin Depends on the Bound Divalent Cation but Not ProfilinBiochemistry, 2001
- Different WASP family proteins stimulate different Arp2/3 complex-dependent actin-nucleating activitiesCurrent Biology, 2001
- Crystal Structure of Arp2/3 ComplexScience, 2001
- The Crystal Structure of Uncomplexed Actin in the ADP StateScience, 2001
- Structure and Function of GelsolinPublished by Springer Nature ,2001
- Domain Movement in Gelsolin: A Calcium-Activated SwitchScience, 1999