Photobleaching Step Counting and Localization for Fluorescence Microscopy - Laboratoire Lumière, Matière et Interfaces
Communication Dans Un Congrès Année : 2024

Photobleaching Step Counting and Localization for Fluorescence Microscopy

Résumé

Fluorescence microscopy is a fundamental tool for studying biological systems at the single-molecule level. In particular, photobleaching step patterns can provide valuable insights into molecule interactions. Several works have proposed an automated and robust way to estimate when photobleaching steps occur. However, most methods are challenging to calibrate by non-experts in statistics or signal processing and struggle with low signal-to-noise ratios. This work introduces a supervised approach to localize photobleaching steps in fluorescent microscopy traces. Our method does not require any calibration but instead needs labels, that is, a few traces where an expert has manually provided the step positions. Our algorithm uses this information to automatically tune a change-point detection method that can reproduce the expert's annotations on new signals. We show on simulated data that our approach better copes with noise than existing ones. We then illustrate how our algorithm can be used to estimate the translation speed of a ribosome.
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Dates et versions

hal-04869324 , version 1 (07-01-2025)

Identifiants

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Charles Truong, Thomas Bugea, Baptiste Bouhet, Guillaume Tresset, François Marquier, et al.. Photobleaching Step Counting and Localization for Fluorescence Microscopy. 2024 46th Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC), Jul 2024, Orlando (Floride), United States. pp.1-4, ⟨10.1109/EMBC53108.2024.10782704⟩. ⟨hal-04869324⟩
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