henhaobio
Sign in

bioRxivBiophysics

Doubling the resolution of fluorescence-lifetime single-molecule localization microscopy with image scanning microscopy

N. Radmacher, O. Nevskyi, J. I. Gallea, J. C. Thiele, I. Gregor, S. O. Rizzoli, J. Enderlein

PDFDOIPreprint

Abstract

In this study, we integrate a single-photon detector array into a Confocal Laser Scanning Microscope (CLSM), enabling the combination of Fluorescence Life-time Single-Molecule Localization Microscopy (FL-SMLM) with Image Scanning Microscopy (ISM). This unique combination delivers a two-fold improvement in lateral localization accuracy for SMLM while maintaining its simplicity. More-over, the addition of lifetime information from our CLSM eliminates chromatic aberration, particularly crucial for achieving few-nanometer resolution in SMLM. Our approach, named Fluorescence Lifetime ISM-SMLM (FL-iSMLM), is demon-strated through direct Stochastic Optical Reconstruction Microscopy (dSTORM) and DNA Point Accumulation for Imaging in Nanoscale Topography (DNA-PAINT) experiments on fluorescently labelled cells, showcasing both resolution enhancement and fluorescence lifetime multiplexing capabilities.

Reproducibility ledger

Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.

Sign in to file a reproducibility report.

Similarity Map
SelectedSame fieldCross-field
THISThiele '20Castello '18Slenders '25Tortarolo '23Slenders '22Batey '24
84% semantic matchBiophysics
J. C. Thiele, D. Helmerich, N. Oleksiievets+5 more·bioRxiv·Aug 25, 2020