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Methods Mol Biol. 2013;1046:145-70. doi: 10.1007/978-1-62703-538-5_9.

Cytoplasmic actin: purification and single molecule assembly assays.

Author information

1
Department of Cellular and Molecular Pharmacology, University of California, San Francisco, CA, USA.

Abstract

The actin cytoskeleton is essential to all eukaryotic cells. In addition to playing important structural roles, assembly of actin into filaments powers diverse cellular processes, including cell motility, cytokinesis, and endocytosis. Actin polymerization is tightly regulated by its numerous cofactors, which control spatial and temporal assembly of actin as well as the physical properties of these filaments. Development of an in vitro model of actin polymerization from purified components has allowed for great advances in determining the effects of these proteins on the actin cytoskeleton. Here we describe how to use the pyrene actin assembly assay to determine the effect of a protein on the kinetics of actin assembly, either directly or as mediated by proteins such as nucleation or capping factors. Secondly, we show how fluorescently labeled phalloidin can be used to visualize the filaments that are created in vitro to give insight into how proteins regulate actin filament structure. Finally, we describe a method for visualizing dynamic assembly and disassembly of single actin filaments and fluorescently labeled actin binding proteins using total internal reflection fluorescence (TIRF) microscopy.

PMID:
23868587
PMCID:
PMC4013826
DOI:
10.1007/978-1-62703-538-5_9
[Indexed for MEDLINE]
Free PMC Article

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