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Onurcan Bektas

Publications and source records attributed to Onurcan Bektas.

3 recordsLinked to original sources

Emergent interactions lead to collective frustration in robotic matter

Artificial intelligence and robotic systems are increasingly deployed as interacting collectives of learning agents. This raises the question of whether robotic matter, where many learning agents interact, shows the emergence of collective behaviour. Here we study a paradigmatic model of robotic matter and show the emergence of a range of complex, collective behaviours. Specifically, we study systems composed of stochastic interacting particles, each endowed with a deep neural network that optimises transitions based on its environment. In a one-dimensional system, we show that robotic matter exhibits complex phenomena arising from emergent interactions, including self-organisation into distinct temporal learning regimes, particle species, and long-lived frustrated states with suboptimal reward. We further identify an abrupt, density-dependent change in collective behaviour. Active matter theory suggests that this phenomenon reflects a phase transition with signatures of criticality. Our results establish robotic matter as a platform for novel non-equilibrium physics.

cond-mat.soft

Self-organized homogenization of flow networks

From the vasculature of animals to the porous media making up batteries, the core task of flow networks is to transport solutes and perfuse all cells or media equally with resources. Yet, living flow networks have a key advantage over porous media: they are adaptive and self-organize their geometry for homogeneous perfusion throughout the network. Here, we show that also artificial flow networks can self-organize toward homogeneous perfusion by the versatile adaption of controlled erosion. Flowing a pulse of cleaving enzyme through a network patterned into an erodible hydrogel, with initial channels disparate in width, we observe a homogenization in channel resistances. Experimental observations are matched with numerical simulations of the diffusion-advection-sorption dynamics of an eroding enzyme within a network. Analyzing transport dynamics theoretically, we show that homogenization only occurs if the pulse of the eroding enzyme lasts longer than the time it takes any channel to equilibrate to the pulse concentration. The equilibration time scale derived analytically is in agreement with simulations. Lastly, we show both numerically and experimentally that erosion leads to the homogenization of complex networks containing loops. Erosion being an omnipresent reaction, our results pave the way for a very versatile self-organized increase in the performance of porous media.

physics.bio-ph

Spatio-temporal patterns of active epigenetic turnover

DNA methylation is a primary layer of epigenetic modification that plays a pivotal role in the regulation of development, aging, and cancer. The concurrent activity of opposing enzymes that mediate DNA methylation and demethylation gives rise to a biochemical cycle and active turnover of DNA methylation. While the ensuing biochemical oscillations have been implicated in the regulation of cell differentiation, their functional role and spatio-temporal dynamics are, however, unknown. In this work, we demonstrate that chromatin-mediated coupling between these local biochemical cycles can lead to the emergence of phase-locked domains, regions of locally synchronized turnover activity, whose coarsening is arrested by genomic heterogeneity. We introduce a minimal model based on stochastic oscillators with constrained long-range and non-reciprocal interactions, shaped by the local chromatin organization. Through a combination of analytical theory and stochastic simulations, we predict both the degree of synchronization and the typical size of emergent phase-locked domains. We qualitatively test these predictions using single-cell sequencing data. Our results show that DNA methylation turnover exhibits surprisingly rich spatio-temporal patterns which may be used by cells to control cell differentiation.

physics.bio-ph