Title of article :
The Interaction of Cofilin with the Actin Filament
Author/Authors :
Diana Y. Wong، نويسنده , , David Sept، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2011
Abstract :
Cofilin is a key actin-binding protein that is critical for controlling the assembly of actin within the cell. Here, we present the results of molecular docking and dynamics studies using a muscle actin filament and human cofilin I. Guided by extensive mutagenesis results and other biophysical and structural studies, we arrive at a model for cofilin bound to the actin filament. This predicted structure agrees very well with electron microscopy results for cofilin-decorated filaments, provides molecular insight into how the known F- and G-actin sites on cofilin interact with the filament, and also suggests new interaction sites that may play a role in cofilin binding. The resulting atomic-scale model also helps us understand the molecular function and regulation of cofilin and provides testable data for future experimental and simulation work.
Keywords :
Mutagenesis , Cytoskeleton , ADF/cofilin , molecular docking
Journal title :
Journal of Molecular Biology
Journal title :
Journal of Molecular Biology