Inverse modeling of time-delayed interactions via the dynamic-entropy formalism.

Although instantaneous interactions are unphysical, a large variety of maximum entropy statistical inference methods match the model-inferred and the empirically measured equal-time correlation functions. Focusing on collective motion of active units, this constraint is reasonable when the interaction timescale is much faster than that of the interacting units, as in starling flocks, yet it fails in a number of counterexamples, as in leukocyte coordination (where signaling proteins diffuse among two cells). Here, we relax this assumption and develop a path integral approach to maximum-entropy framework, which includes delay in signaling.

Steric interactions and out-of-equilibrium processes control the internal organization of bacteria.

Despite the absence of a membrane-enclosed nucleus, the bacterial DNA is typically condensed into a compact body-the nucleoid. This compaction influences the localization and dynamics of many cellular processes including transcription, translation, and cell division. Here, we develop a model that takes into account steric interactions among the components of the transcriptional-translational machinery (TTM) and out-of-equilibrium effects of messenger RNA (mRNA) transcription, translation, and degradation, to explain many observed features of the nucleoid.

Two timescales control the creation of large protein aggregates in cells.

Protein aggregation is of particular interest because of its connection with many diseases and disorders. Many factors can alter the dynamics and result of this process, one of them being the diffusivity of the monomers and aggregates in the system. Here, we study experimentally and theoretically an aggregation process in cells, and we identify two distinct physical timescales that set the number and size of aggregates.

A statistical inference approach to reconstruct intercellular interactions in cell migration experiments.

Migration of cells can be characterized by two prototypical types of motion: individual and collective migration. We propose a statistical inference approach designed to detect the presence of cell-cell interactions that give rise to collective behaviors in cell motility experiments. This inference method has been first successfully tested on synthetic motional data and then applied to two experiments.

Spatial organization of bacterial transcription and translation.

In bacteria such as Escherichia coli, DNA is compacted into a nucleoid near the cell center, whereas ribosomes-molecular complexes that translate mRNAs into proteins-are mainly localized to the poles. We study the impact of this spatial organization using a minimal reaction-diffusion model for the cellular transcriptional-translational machinery. Although genome-wide mRNA-nucleoid segregation still lacks experimental validation, our model predicts that [Formula: see text] of mRNAs are segregated to the poles.

Entropic effects in a nonequilibrium system: Flocks of birds.

When European starlings come together to form a flock, the distribution of their individual velocities narrows around the mean velocity of the flock. We argue that, in a broad class of models for the joint distribution of positions and velocities, this narrowing generates an entropic effect that opposes the cohesion of the flock. The strength of this effect depends strongly on the nature of the interactions among birds: If birds are coupled to a fixed number of neighbors, the entropic forces are weak, while if they couple to all other birds within a fixed distance, the entropic effects are sufficient to tear a flock apart.

Non-perturbative effects in spin glasses.

We present a numerical study of an Ising spin glass with hierarchical interactions--the hierarchical Edwards-Anderson model with an external magnetic field (HEA). We study the model with Monte Carlo (MC) simulations in the mean-field (MF) and non-mean-field (NMF) regions corresponding to d ≥ 4 and d < 4 for the d-dimensional ferromagnetic Ising model respectively. We compare the MC results with those of a renormalization-group (RG) study where the critical fixed point is treated as a perturbation of the MF one, along the same lines as in the -expansion for the Ising model.

Enzyme clustering accelerates processing of intermediates through metabolic channeling.

We present a quantitative model to demonstrate that coclustering multiple enzymes into compact agglomerates accelerates the processing of intermediates, yielding the same efficiency benefits as direct channeling, a well-known mechanism in which enzymes are funneled between enzyme active sites through a physical tunnel. The model predicts the separation and size of coclusters that maximize metabolic efficiency, and this prediction is in agreement with previously reported spacings between coclusters in mammalian cells. For direct validation, we study a metabolic branch point in Escherichia coli and experimentally confirm the model prediction that enzyme agglomerates can accelerate the processing of a shared intermediate by one branch, and thus regulate steady-state flux division.

Inverse spin glass and related maximum entropy problems.

If we have a system of binary variables and we measure the pairwise correlations among these variables, then the least structured or maximum entropy model for their joint distribution is an Ising model with pairwise interactions among the spins. Here we consider inhomogeneous systems in which we constrain, for example, not the full matrix of correlations, but only the distribution from which these correlations are drawn. In this sense, what we have constructed is an inverse spin glass: rather than choosing coupling constants at random from a distribution and calculating correlations, we choose the correlations from a distribution and infer the coupling constants.

Extreme value statistics distributions in spin glasses.

We study the probability distribution of the pseudocritical temperature in a mean-field and in a short-range spin-glass model: the Sherrington-Kirkpatrick and the Edwards-Anderson (EA) model. In both cases, we put in evidence the underlying connection between the fluctuations of the pseudocritical point and the extreme value statistics of random variables. For the Sherrington-Kirkpatrick model, both with Gaussian and binary couplings, the distribution of the pseudocritical temperature is found to be the Tracy-Widom distribution.

Renormalization-group computation of the critical exponents of hierarchical spin glasses: large-scale behavior and divergence of the correlation length.

In a recent work [M. Castellana and G. Parisi, Phys.

Renormalization group computation of the critical exponents of hierarchical spin glasses.

The large scale behavior of the simplest non-mean-field spin-glass system is analyzed, and the critical exponent related to the divergence of the correlation length is computed at two loops within the ε-expansion technique with two independent methods. The techniques presented show how the underlying ideas of the renormalization group apply also in this disordered model, in such a way that an ε-expansion can be consistently set up. By pushing such calculation to high orders in ε, a consistent non-mean-field theory for such disordered system could be established, giving a substantial contribution the development of a predictive theory for real spin glasses.

Hierarchical random energy model of a spin glass.

We introduce a random energy model on a hierarchical lattice where the interaction strength between variables is a decreasing function of their mutual hierarchical distance, making it a non-mean-field model. Through small coupling series expansion and a direct numerical solution of the model, we provide evidence for a spin-glass condensation transition similar to the one occurring in the usual mean-field random energy model. At variance with the mean field, the high temperature branch of the free-energy is nonanalytic at the transition point.