Complex patterns: building a bridge from the large to the small
A new theory enables the simulation of complex pattern formation in biological systems across different spatial and temporal scales
LMU / v.zingn
Numerical computations in minutes instead of months
The scientists illustrated the potential of their approach with the Min protein system, a paradigmatic model for biological pattern formation. The bacterium E. coli uses various Min proteins circulating in a cell to determine at which location cell division takes place. A decisive factor here is that the proteins involved occur at different frequencies depending on their location in the cell and chemical state – which is to say, they have a variety of different densities. “We’ve now managed to reduce the complexity of this system by developing a theory that is based solely on the total densities of the proteins, such that we can completely mirror the dynamics of pattern formation,” says Frey. “This is a huge reduction. The numerical computations are now accomplished in a matter of minutes instead of months.”
The researchers were able to experimentally confirm theoretical predictions of the model, according to which distribution of the proteins depends on the geometry of the environment. They did this by reconstructing the Min protein system in an in-vitro flow cell, with the results showing the same protein patterns as were revealed in the simulation. “Such reconstruction of information at a small length scale from reduced dynamics at the macroscopic level opens up new pathways for a better understanding of complex multiscale systems, which occur in a broad range of physical systems,” says Frey.
Original publication
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