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Autophagy pp 231-242 | Cite as

Correlative Live-Cell Imaging and Super-Resolution Microscopy of Autophagy

  • Eleftherios Karanasios
Protocol
Part of the Methods in Molecular Biology book series (MIMB, volume 1880)

Abstract

Correlative live-cell imaging and super-resolution microscopy of autophagy was developed to combine the temporal resolution of time-lapse fluorescence microscopy with the spatial resolution of super-resolution microscopy. HEK293 cells that express recombinant proteins of interest fused to fluorescent tags are imaged live to capture the formation of autophagosomes, fixed on stage to “snap-freeze” these structures, stained with appropriate antibodies, relocated, and imaged at super resolution by direct stochastic optical reconstruction microscopy. This chapter provides an easy-to-follow protocol along with practical tips and background information to help set up and perform an experiment.

Key words

Autophagy Autophagosome Endoplasmic reticulum Membrane trafficking Time-lapse fluorescence microscopy Super-resolution microscopy dSTORM HEK293 

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Copyright information

© Springer Science+Business Media, LLC, part of Springer Nature 2019

Authors and Affiliations

  • Eleftherios Karanasios
    • 1
  1. 1.Department of Basic and Clinical NeuroscienceInstitute of Psychiatry, Psychology and Neuroscience, King’s College London, Maurice Wohl Clinical Neuroscience InstituteLondonUK

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