Researcher profile

Hugues Berry

Hugues Berry contributes to research discovery and scholarly infrastructure.

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Published work

3 published item(s)

preprint2026arXiv

Accounting for Missed Events in the Bayesian Modeling of IP3R Multimodal Gating

The Inositol 1,4,5-trisphosphate receptor channel (IP 3 R) is an important calcium channel involved in calcium-induced calcium release, playing a prominent role in intracellular calcium signaling. However, accurately characterizing its gating behavior remains a challenge, particularly due to the temporal resolution of patch clamp techniques that is not large enough to detect all short-lived events. This limitation can significantly bias the inference of kinetic models describing the receptor activity. To address this issue, we focused on the quantitative analysis of IP 3 R gating behavior using patch clamp data, with particular attention to missed events. We modeled IP 3 R channel gating using Hierarchical Markov chains and used a Bayesian approach that integrates missed event correction directly into the likelihood function, enabling more accurate parameter inference and model evaluation. We show that accounting for missed events deeply clarifies the multi-modal model that emerges from model selection. In this new model, the Park and Drive modes both consist of the same 3-state Markov model, with mode-dependent kinetic parameters: the Drive mode stabilizes the closed state directly connected to the open one, whereas the Park mode stabilizes the other closed state, that is not connected to the open one. Intermediate Ca 2+ concentrations are found to strongly depress the Drive to Park transition rate, so that the IP 3 R channel undergoes frequent transitions to the Park mode only for __ 50 nM or micromolar Ca 2+ concentrations. Overall, our approach provides a refined perspective on IP 3 R channel modeling and highlights the critical importance of accounting for missed events upon model selection based on single-channel recordings.

preprint2020arXiv

Anomalous subdiffusion in living cells: bridging the gap between experiments and realistic models through collaborative challenges

The life of a cell is governed by highly dynamical microscopic processes. Two notable examples are the diffusion of membrane receptors and the kinetics of transcription factors governing the rates of gene expression. Different fluorescence imaging techniques have emerged to study molecular dynamics. Among them, fluorescence correlation spectroscopy (FCS) and single-particle tracking (SPT) have proven to be instrumental to our understanding of cell dynamics and function. The analysis of SPT and FCS is an ongoing effort, and despite decades of work, much progress remains to be done. In this paper, we give a quick overview of the existing techniques used to analyze anomalous diffusion in cells and propose a collaborative challenge to foster the development of state-of-the-art analysis algorithms. We propose to provide labelled (training) and unlabelled (evaluation) simulated data to competitors all over the world in an open and fair challenge. The goal is to offer unified data benchmarks based on biologically-relevant metrics in order to compare the diffusion analysis software available for the community.