Alternative mechanisms of structuring biomembranes: Self-assembly vs. self-organization
Karin John, Markus Baer
Abstract
We study two mechanisms for the formation of protein patterns near membranes of living cells by mathematical modelling. Self-assembly of protein domains by electrostatic lipid-protein interactions is contrasted with self-organization due to a nonequilibrium biochemical reaction cycle of proteins near the membrane. While both processes lead eventually to quite similar patterns, their evolution occurs on very different length and time scales. Self-assembly produces periodic protein patterns on a spatial scale below 0.1 micron in a few seconds followed by extremely slow coarsening, whereas self-organization results in a pattern wavelength comparable to the typical cell size of 100 micron within a few minutes suggesting different biological functions for the two processes.
Create a lesson
Related papers
Fragmented uptake drives lipid accumulation in macrophage cannibalistic efferocytosis
Keith L. Chambers
Modeling Tissue Detachment and Rupture Using an Extended Vertex Model with T2-inverse Transitions
Shota Nishimoto, Yuichi Togashi
Coarse-Graining Agent-Based Models of Bacterial Infections
Wesley J. M. Ridgway, Raymond J. Spiteri
3D hybrid cellular Potts model with a discrete deformable fiber network: modeling cell contraction and extracellular matrix remodeling
Koen A. E. Keijzer, Roeland M. H. Merks
Hydrodynamic theories of chemotaxis-driven invasion in proliferating cell populations
Giulia L. Celora, Martina Conte
Population Structures with Positive Feedback and Asymmetric Division
Gabriel Dooley, Camden Kilton, Brynley Needham et al.