Mathematical modeling of myosin induced bistability of lamellipodial fragments (Q504051): Difference between revisions

From MaRDI portal
Import240304020342 (talk | contribs)
Set profile property.
ReferenceBot (talk | contribs)
Changed an Item
 
(2 intermediate revisions by 2 users not shown)
Property / OpenAlex ID
 
Property / OpenAlex ID: W2344959949 / rank
 
Normal rank
Property / arXiv ID
 
Property / arXiv ID: 1511.08602 / rank
 
Normal rank
Property / cites work
 
Property / cites work: An extended filament based lamellipodium model produces various moving cell shapes in the presence of chemotactic signals / rank
 
Normal rank
Property / cites work
 
Property / cites work: Mathematics of cell motility: Have we got its number? / rank
 
Normal rank
Property / cites work
 
Property / cites work: Derivation of a model for symmetric lamellipodia with instantaneous cross-link turnover / rank
 
Normal rank
Property / cites work
 
Property / cites work: Multiscale Two-Dimensional Modeling of a Motile Simple-Shaped Cell / rank
 
Normal rank

Latest revision as of 07:42, 13 July 2024

scientific article
Language Label Description Also known as
English
Mathematical modeling of myosin induced bistability of lamellipodial fragments
scientific article

    Statements

    Mathematical modeling of myosin induced bistability of lamellipodial fragments (English)
    0 references
    0 references
    0 references
    0 references
    25 January 2017
    0 references
    The article considers a model for the dynamics of lamelliapodial filamens orerating with the system of actin-myosin compartments and their interactions. The principal structure is a net of crossing actin filaments, which are pair-wisely connected by myosin links; in addition, these connection can be created and broken in dependence on the forces acting on them. The model construction takes into account energy contribution of various configurations and results in the system of Euler-Lagrange equations obtained via the variational approach that results in the biologically relevant bistable solution. This construction is illustrated with the numerical simulation able to demonstrate that the modelled cell fragments can remain stationary or be in a moving state.
    0 references
    actin
    0 references
    myosin
    0 references
    mathematical model
    0 references
    cytoskeleton
    0 references

    Identifiers

    0 references
    0 references
    0 references
    0 references
    0 references
    0 references
    0 references
    0 references