A light-weight, data-driven segmentation method for multi-state Brownian trajectories

Abstract Single-particle tracking methods have emerged as a crucial tool for the characterisation of dynamical and diffusive processes in a range of biological and synthetic systems. Here, we propose a simple and light-weight yet accurate method for the segmentation of multi-state Brownian trajectories based on an optimised Gaussian filtering of the displacement time series combined with an automated fitting to a Gaussian mixture model. We verify our method using synthetic, 2-state Brownian trajectories and show that our method provides high levels of accuracy in terms of segmentation and the estimation of self-diffusion coefficients for reasonably well-separated values of the diffusion coefficients. We furthermore demonstrate the feasibility of our method on experimental systems using single-particle tracking data for diffusing membrane proteins bound to a supported lipid bilayer. Compared to methods based on deep learning or hidden Markov models, our method imposes a much lower computational load, making it suitable for fast and accurate online processing of single-particle trajectories from microscopy images.

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Publication Details

Journal
npj Biological Physics and Mechanics.
Published
2026-05-08
DOI
https://doi.org/10.1038/s44341-026-00037-7
Primary Topic
Advanced Fluorescence Microscopy Techniques
Type
article
Field-Weighted Citation Impact
0.00

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article

A light-weight, data-driven segmentation method for multi-state Brownian trajectories

Joakim Stenhammar, Tobias Ambjörnsson, Tommy Dam, Peter Jönsson et al.
npj Biological Physics and Mechanics.
Advanced Fluorescence Microscopy Techniques
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A light-weight, data-driven segmentation method for multi-state Brownian trajectories

Joakim Stenhammar, Tobias Ambjörnsson, Tommy Dam, Peter Jönsson, Jason Lewis, Ismail El Korde, Erik Clarkson
article en

Abstract

Abstract Single-particle tracking methods have emerged as a crucial tool for the characterisation of dynamical and diffusive processes in a range of biological and synthetic systems. Here, we propose a simple and light-weight yet accurate method for the segmentation of multi-state Brownian trajectories based on an optimised Gaussian filtering of the displacement time series combined with an automated fitting to a Gaussian mixture model. We verify our method using synthetic, 2-state Brownian trajectories and show that our method provides high levels of accuracy in terms of segmentation and the estimation of self-diffusion coefficients for reasonably well-separated values of the diffusion coefficients. We furthermore demonstrate the feasibility of our method on experimental systems using single-particle tracking data for diffusing membrane proteins bound to a supported lipid bilayer. Compared to methods based on deep learning or hidden Markov models, our method imposes a much lower computational load, making it suitable for fast and accurate online processing of single-particle trajectories from microscopy images.

npj Biological Physics and Mechanics.Vol. 3(1)
Lund University (SE), University of Oxford (GB)
Lunds Universitet, Knut och Alice Wallenbergs Stiftelse, Vetenskapsrådet
Openalex Percentile: Top 5%
Advanced Fluorescence Microscopy Techniques
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