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Nino Lauber

Publications and source records attributed to Nino Lauber.

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Thermodynamic ranking of pathways in reaction networks

One of the puzzles left open by energetic analyses of irreversible stochastic processes is that boundary conditions that prevent the performance of work or the dissipation of heat make no contribution to an entropy-production budget; yet we see ubiquitously in both engineered and living systems that both transient and persistent energy costs are paid to create and maintain such boundaries. We wish to know whether there are inherent limits for the costs of such phenomena, and common units in which those can be traded off against more familiar costs measured in terms of heat dissipation. We give this problem a concrete framing in the context of CRNs, for the problem of extracting a topologically restricted pathway from a larger distributed network, through activation of some reactions and selective elimination of others. We define a thermodynamic cost function for pathways derived from large-deviation theory of stochastic CRNs, which decomposes into two components: an ongoing maintenance cost to sustain a NESS, and a restriction cost, quantifying the ongoing improbability of neutralizing reactions outside the specified pathway. Applying this formalism to detailed-balanced CRNs in the linear response regime, we make use of their formal equivalence to electrical circuits. We prove that the resistance of a CRN decreases as reactions are added that support the throughput current, and that the maintenance cost, the restriction cost, and the thermodynamic cost of nested pathways are bounded below by those of their hosting network. For small CRNs, we show how catalytic and inhibitory mechanisms can drastically alter pathway costs, enabling unfavorable pathways to become favorable and approach the cost of the hosting pathway. Our results provide insights into the thermodynamic principles governing open CRNs and offer a foundation for understanding the evolution of metabolic networks.

q-bio.MN

Modelling spatial constraints and scaling effects of catalyst phase separation on linear pathway kinetics

Chemical reactions are usually studied under the assumption that both substrates and catalysts are well mixed (WM) throughout the system. Although this is often applicable to test-tube experimental conditions, it is not realistic in cellular environments, where biomolecules can undergo liquid-liquid phase separation (LLPS) and form condensates, leading to important functional outcomes, including the modulation of catalytic action. Similar processes may also play a role in protocellular systems, like primitive coacervates, or in membrane-assisted prebiotic pathways. Here we explore whether the de-mixing of catalysts could lead to the formation of micro-environments that influence the kinetics of a linear (multi-step) reaction pathway, as compared to a WM system. We implemented a general lattice model to simulate LLPS of an ensemble of different catalysts and extended it to include diffusion and a sequence of reactions of small substrates. We carried out a quantitative analysis of how the phase separation of the catalysts affects reaction times depending on the affinity between substrates and catalysts, the length of the reaction pathway, the system size, and the degree of homogeneity of the condensate. A key aspect underlying the differences reported between the two scenarios is that the scale invariance observed in the WM system is broken by condensation processes. The main theoretical implications of our results for mean-field chemistry are drawn, extending the mass action kinetics scheme to include substrate initial hitting times to reach the catalysts condensate. We finally test this approach by considering open non-linear conditions, where we successfully predict, through microscopic simulations, that phase separation inhibits chemical oscillatory behaviour, providing a possible explanation for the marginal role that this complex dynamic behaviour plays in real metabolisms.

cond-mat.stat-mech