Presentation
13 March 2024 The BrightEyes project: image scanning microscopy meets single-molecule tracking and imaging
Author Affiliations +
Abstract
Fluorescence laser-scanning microscopy (FLSM) is a widely utilized tool in life-science research. In recent years, this technique has undergone a profound transformation, thanks to the introduction of novel single-photon avalanche diode (SPAD) array detectors. This study reveals the exciting possibilities of combining the SPAD array detector with single-molecule techniques. We propose a real-time single-molecule tracking architecture, where the SPAD array effortlessly localizes the molecule of interest, and the beam scanning architecture effectively maintains the molecule at the center of the microscope's detection volume. This approach enables comprehensive three-dimensional tracking throughout the entire cell, offering valuable insights into molecular nano-environments, interactions, and structural changes through fluorescence lifetime information. Furthermore, utilizing the same FLSM system, we present a novel sequential structure illumination single-molecule localization microscope (similar to MINFLUX). This advanced technique achieves localization precision in the few-nanometer range while simultaneously providing the molecule's fluorescence lifetime.
Conference Presentation
© (2024) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Andrea Bucci, Sanket Patil, Luca Bega, Marcus Olvier Held, Eli Slenders, and Giuseppe Vicidomini "The BrightEyes project: image scanning microscopy meets single-molecule tracking and imaging", Proc. SPIE PC12849, Single Molecule Spectroscopy and Superresolution Imaging XVII, PC1284907 (13 March 2024); https://doi.org/10.1117/12.3001822
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KEYWORDS
Fluorescence

Laser soldering

Single photon avalanche diodes

3D tracking

Molecules

Imaging spectroscopy

Imaging systems

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