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Anastasios Matzavinos

Publications and source records attributed to Anastasios Matzavinos.

9 recordsLinked to original sources

On the role of fractional Brownian motion in models of chemotaxis and stochastic gradient ascent

Cell migration often exhibits long-range temporal correlations and anomalous diffusion, even in the absence of external guidance cues such as chemical gradients or topographical constraints. This raises a fundamental question: do such correlations enhance a cell's ability to navigate complex environments? In this work, we explore how temporally correlated noise (modeled using fractional Brownian motion) influences chemotactic search dynamics. Through computational experiments, we show that superdiffusive motion, when combined with gradient-driven migration, enables robust exploration of the chemoattractant landscape. Cells reliably reach the global maximum of the concentration field, even in the presence of spatial noise, secondary cues, or irregular signal geometry. We quantify this behavior by analyzing the distribution of first hitting times under varying degrees of temporal correlation. Notably, our results are consistent across diverse conditions, including flat and curved substrates, and scenarios involving both primary and self-generated chemotactic signals. Beyond biological implications, these findings also offer insight into the design of optimization and sampling algorithms that benefit from structured stochasticity.

q-bio.QM

Bayesian uncertainty quantification for micro-swimmers with fully resolved hydrodynamics

Due to the computational complexity of micro-swimmer models with fully resolved hydrodynamics, parameter estimation has been prohibitively expensive. Here, we describe a Bayesian uncertainty quantification framework that is highly parallelizable, making parameter estimation for complex forward models tractable. Using noisy in-silico data for swimmers, we demonstrate the methodology's robustness in estimating the fluid and elastic swimmer parameters. Our proposed methodology allows for analysis of real data and demonstrates potential for parameter estimation for various types of micro-swimmers. Better understanding the movement of elastic micro-structures in a viscous fluid could aid in developing artificial micro-swimmers for bio-medical applications as well as gain a fundamental understanding of the range of parameters that allow for certain motility patterns.

q-bio.QM

Data-driven prediction and origin identification of epidemics in population networks

Effective intervention strategies for epidemics rely on the identification of their origin and on the robustness of the predictions made by network disease models. We introduce a Bayesian uncertainty quantification framework to infer model parameters for a disease spreading on a network of communities from limited, noisy observations; the state-of-the-art computational framework compensates for the model complexity by exploiting massively parallel computing architectures. Using noisy, synthetic data, we show the potential of the approach to perform robust model fitting and additionally demonstrate that we can effectively identify the disease origin via Bayesian model selection. As disease-related data are increasingly available, the proposed framework has broad practical relevance for the prediction and management of epidemics.

q-bio.PE

Dissipative particle dynamics simulation of critical pore size in a lipid bilayer membrane

We investigate with computer simulations the critical radius of pores in a lipid bilayer membrane. Ilton et al. (2016) recently showed that nucleated pores in a homopolymer film can increase or decrease in size, depending on whether they are larger or smaller than a critical size which scales linearly with film thickness. Using dissipative particle dynamics, a particle-based simulation method, we investigate the same scenario for a lipid bilayer membrane whose structure is determined by lipid-water interactions. We simulate a perforated membrane in which holes larger than a critical radius grow, while holes smaller than the critical radius close, as in the experiment of Ilton et al. (2016). By altering system parameters such as the number of particles per lipid and the periodicity, we also describe scenarios in which pores of any initial size can seal or even remain stable, showing a fundamental difference in the behavior of lipid membranes from polymer films.

cond-mat.soft

Moran-type bounds for the fixation probability in a frequency-dependent Wright-Fisher model

We study stochastic evolutionary game dynamics in a population of finite size. Individuals in the population are divided into two dynamically evolving groups. The structure of the population is formally described by a Wright-Fisher type Markov chain with a frequency dependent fitness. In a strong selection regime that favors one of the two groups, we obtain qualitatively matching lower and upper bounds for the fixation probability of the advantageous population. In the infinite population limit we obtain an exact result showing that a single advantageous mutant can invade an infinite population with a positive probability. We also give asymptotically sharp bounds for the fixation time distribution.

math.PR

Random Walks in a Sparse Random Environment

We introduce random walks in a sparse random environment on $\mathbb Z$ and investigate basic asymptotic properties of this model, such as recurrence-transience, asymptotic speed, and limit theorems in both the transient and recurrent regimes. The new model combines features of several existing models of random motion in random media and admits a transparent physical interpretation. More specifically, a random walk in a sparse random environment can be characterized as a "locally strong" perturbation of a simple random walk by a random potential induced by "rare impurities," which are randomly distributed over the integer lattice. Interestingly, in the critical (recurrent) regime, our model generalizes Sinai's scaling of $(\log n)^2$ for the location of the random walk after $n$ steps to $(\log n)^\alpha,$ where $\alpha>0$ is a parameter determined by the distribution of the distance between two successive impurities. Similar scaling factors have appeared in the literature in different contexts and have been discussed in [28] and [30].

math.PR

Homogenization of oxygen transport in biological tissues

In this paper, we extend previous work on the mathematical modeling of oxygen transport in biological tissues (Matzavinos et al., 2009). Specifically, we include in the modeling process the arterial and venous microstructure within the tissue by means of homogenization techniques. We focus on the two-layer tissue architecture investigated in (Matzavinos et al., 2009) in the context of abdominal tissue flaps that are commonly used for reconstructive surgery. We apply two-scale convergence methods and unfolding operator techniques to homogenize the developed microscopic model, which involves different unit-cell geometries in the two distinct tissue layers (skin layer and fat tissue) to account for different arterial branching patterns.

math.AP

Stochastic homogenization of the Keller-Segel chemotaxis system

In this paper, we focus on the Keller-Segel chemotaxis system in a random heterogeneous domain. We assume that the corresponding diffusion and chemotaxis coefficients are given by stationary ergodic random fields and apply stochastic two-scale convergence methods to derive the homogenized macroscopic equations. In establishing our results, we also derive a priori estimates for the Keller-Segel system that rely only on the boundedness of the coefficients; in particular, no differentiability assumption on the diffusion and chemotaxis coefficients for the chemotactic species is required. Finally, we prove the convergence of a periodization procedure for approximating the homogenized macroscopic coefficients.

math.AP

On a species survival model

In this paper we provide some sharp asymptotic results for a stochastic model of species survival recently proposed by Guiol, Marchado, and Schinazi.

math.PR