AbstractAt 37°C, the α-actinin-F-actin binding isotherm is anomalous. In 6.7% polyethylene glycol 6000, concomitantly with the formation of actin bundles, the binding isotherm becomes hyperbolic (Kdiss. = 11.3 μM). α-Actinin increases the rigidity of the networks formed by actin bundles in polyethylene glycol and by paracrystalline actin in 16 mM MgCl2 but not by F-actin. It is proposed that in the cell α-actinin functions are mostly carried on by interaction with actin bundles
While actin bundles are used by living cells for structural fortification, the microscopic origin of...
The interaction of alpha-actinin from chicken gizzard with F-actin is quite complex. The apparent di...
AbstractThe purpose of this study was to address the paradox of calponin localization with α-actinin...
AbstractAt 37°C, the α-actinin-F-actin binding isotherm is anomalous. In 6.7% polyethylene glycol 60...
At 37 degrees C, the alpha-actin-F-actin binding isotherm is anomalous. In 6.7% polyethylene glycol ...
AbstractMeasurement of the binding equilibrium for the interaction of α-actinin with F-actin is comp...
Proteins that cross-link actin filaments can either form bundles of parallel filaments or isotropic ...
AbstractAt 37°C, in the presence of 6% (wv) polyethylene glycol 6000, 30 nM α-actinin from chicken g...
AbstractActin filament length distribution in cells is often regulated to fit specific tasks. In com...
The usual rate of actin polymerization is increased if one starts from action nuclei. We have notice...
The interaction of alpha-actinin with lipid films and actin filaments was investigated. First alpha-...
AbstractCell morphology is controlled by the actin cytoskeleton organization and mechanical properti...
While actin bundles are used by living cells for structural fortification, the microscopic origin of...
While actin bundles are used by living cells for structural fortification, the microscopic origin of...
While actin bundles are used by living cells for structural fortification, the microscopic origin of...
While actin bundles are used by living cells for structural fortification, the microscopic origin of...
The interaction of alpha-actinin from chicken gizzard with F-actin is quite complex. The apparent di...
AbstractThe purpose of this study was to address the paradox of calponin localization with α-actinin...
AbstractAt 37°C, the α-actinin-F-actin binding isotherm is anomalous. In 6.7% polyethylene glycol 60...
At 37 degrees C, the alpha-actin-F-actin binding isotherm is anomalous. In 6.7% polyethylene glycol ...
AbstractMeasurement of the binding equilibrium for the interaction of α-actinin with F-actin is comp...
Proteins that cross-link actin filaments can either form bundles of parallel filaments or isotropic ...
AbstractAt 37°C, in the presence of 6% (wv) polyethylene glycol 6000, 30 nM α-actinin from chicken g...
AbstractActin filament length distribution in cells is often regulated to fit specific tasks. In com...
The usual rate of actin polymerization is increased if one starts from action nuclei. We have notice...
The interaction of alpha-actinin with lipid films and actin filaments was investigated. First alpha-...
AbstractCell morphology is controlled by the actin cytoskeleton organization and mechanical properti...
While actin bundles are used by living cells for structural fortification, the microscopic origin of...
While actin bundles are used by living cells for structural fortification, the microscopic origin of...
While actin bundles are used by living cells for structural fortification, the microscopic origin of...
While actin bundles are used by living cells for structural fortification, the microscopic origin of...
The interaction of alpha-actinin from chicken gizzard with F-actin is quite complex. The apparent di...
AbstractThe purpose of this study was to address the paradox of calponin localization with α-actinin...