We present 3D dynamic Monte-Carlo simulations of the growth of an actin network close to an obstacle coated with Wiskott-Aldrich syndrome protein (WASP), an inducer of actin branching. Our simulations incorporate both elasticity and relaxation of the actin tail, thus allowing for local network compression. Whilst steady state motility derives mainly from polymerization at the leading edge, nonthermal stored elastic energy and retrograde flow are observed in a thin slab of material close to the obstacle. We observe a crossover from steady to hopping bead motion as the branching rate is decreased
Actomyosin networks give cells the ability to move and divide. These networks contract and expand wh...
Cytoskeletal networks, which are essentially motor-filament assemblies, play a major role in many de...
We propose a mathematical model of the actin-based propulsion of spatially extended obstacles. It st...
<div><p>Two theoretical models dominate current understanding of actin-based propulsion: microscopic...
Two theoretical models dominate current understanding of actin-based propulsion: microscopic polymer...
AbstractWe present the first numerical simulation of actin-driven propulsion by elastic filaments. S...
ABSTRACT We present the first numerical simulation of actin-driven propulsion by elastic filaments. ...
International audienceCells use their dynamic actin network to control their mechanics and motility....
We study force generation and actin filament dynamics using stochastic and deterministic methods. Fi...
We consider the growth of a semiflexible clamped polymer, or fibre, incident at an angle on a fluctu...
Eukaryotic cells assemble viscoelastic networks of crosslinked actin filaments to control their shap...
International audienceMany processes in eukaryotic cells, including cell motility, rely on the growt...
Many processes in eukaryotic cells, including the crawling motion of the whole cell, rely on the gro...
ABSTRACTThe growth of an actin network against an obstacle that stimulates branching locally is stud...
AbstractMany processes in eukaryotic cells, including the crawling motion of the whole cell, rely on...
Actomyosin networks give cells the ability to move and divide. These networks contract and expand wh...
Cytoskeletal networks, which are essentially motor-filament assemblies, play a major role in many de...
We propose a mathematical model of the actin-based propulsion of spatially extended obstacles. It st...
<div><p>Two theoretical models dominate current understanding of actin-based propulsion: microscopic...
Two theoretical models dominate current understanding of actin-based propulsion: microscopic polymer...
AbstractWe present the first numerical simulation of actin-driven propulsion by elastic filaments. S...
ABSTRACT We present the first numerical simulation of actin-driven propulsion by elastic filaments. ...
International audienceCells use their dynamic actin network to control their mechanics and motility....
We study force generation and actin filament dynamics using stochastic and deterministic methods. Fi...
We consider the growth of a semiflexible clamped polymer, or fibre, incident at an angle on a fluctu...
Eukaryotic cells assemble viscoelastic networks of crosslinked actin filaments to control their shap...
International audienceMany processes in eukaryotic cells, including cell motility, rely on the growt...
Many processes in eukaryotic cells, including the crawling motion of the whole cell, rely on the gro...
ABSTRACTThe growth of an actin network against an obstacle that stimulates branching locally is stud...
AbstractMany processes in eukaryotic cells, including the crawling motion of the whole cell, rely on...
Actomyosin networks give cells the ability to move and divide. These networks contract and expand wh...
Cytoskeletal networks, which are essentially motor-filament assemblies, play a major role in many de...
We propose a mathematical model of the actin-based propulsion of spatially extended obstacles. It st...