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Two-color nanoscopy of organelles for extended times with HIDE probes

Ling Chu, Jonathan Tyson, Juliana Shaw, Félix Rivera-Molina, Anthony J. Koleske, Alanna Schepartz, Derek Toomre

2020Nature Communications37 citationsDOIOpen Access PDF

Abstract

Performing multi-color nanoscopy for extended times is challenging due to the rapid photobleaching rate of most fluorophores. Here we describe a new fluorophore (Yale-595) and a bio-orthogonal labeling strategy that enables two-color super-resolution (STED) and 3D confocal imaging of two organelles simultaneously for extended times using high-density environmentally sensitive (HIDE) probes. Because HIDE probes are small, cell-permeant molecules, they can visualize dual organelle dynamics in hard-to-transfect cell lines by super-resolution for over an order of magnitude longer than with tagged proteins. The extended time domain possible using these tools reveals dynamic nanoscale targeting between different organelles.

Topics & Concepts

STED microscopyPhotobleachingOrganelleFluorophoreConfocalFluorescence recovery after photobleachingMicroscopyConfocal microscopySuper-resolution microscopyLive cell imagingResolution (logic)FluorescenceBiophysicsFluorescence microscopeNanotechnologyChemistryMaterials sciencePhysicsComputer scienceOpticsStimulated emissionBiologyCellArtificial intelligenceBiochemistryLaserAdvanced Fluorescence Microscopy TechniquesRNA Interference and Gene DeliveryAdvanced biosensing and bioanalysis techniques
Two-color nanoscopy of organelles for extended times with HIDE probes | Litcius