The LC3B FRET biosensor monitors the modes of action of ATG4B during autophagy in living cells

Autophagy. 2023 Aug;19(8):2275-2295. doi: 10.1080/15548627.2023.2179845. Epub 2023 Feb 22.

Abstract

Although several mechanisms of macroautophagy/autophagy have been dissected in the last decade, following this pathway in real time remains challenging. Among the early events leading to its activation, the ATG4B protease primes the key autophagy player MAP1LC3B/LC3B. Given the lack of reporters to follow this event in living cells, we developed a Förster's resonance energy transfer (FRET) biosensor responding to the priming of LC3B by ATG4B. The biosensor was generated by flanking LC3B within a pH-resistant donor-acceptor FRET pair, Aquamarine-tdLanYFP. We here showed that the biosensor has a dual readout. First, FRET indicates the priming of LC3B by ATG4B and the resolution of the FRET image makes it possible to characterize the spatial heterogeneity of the priming activity. Second, quantifying the number of Aquamarine-LC3B puncta determines the degree of autophagy activation. We then showed that there are pools of unprimed LC3B upon ATG4B downregulation, and the priming of the biosensor is abolished in ATG4B knockout cells. The lack of priming can be rescued with the wild-type ATG4B or with the partially active W142A mutant, but not with the catalytically dead C74S mutant. Moreover, we screened for commercially-available ATG4B inhibitors, and illustrated their differential mode of action by implementing a spatially-resolved, broad-to-sensitive analysis pipeline combining FRET and the quantification of autophagic puncta. Finally, we uncovered the CDK1-dependent regulation of the ATG4B-LC3B axis at mitosis. Therefore, the LC3B FRET biosensor paves the way for a highly-quantitative monitoring of the ATG4B activity in living cells and in real time, with unprecedented spatiotemporal resolution.Abbreviations: Aqua: aquamarine; ATG: autophagy related; AURKA: aurora kinase A; BafA1: bafilomycin A1; CDK1: cyclin dependent kinase 1; DKO: double knockout; FLIM: fluorescence lifetime imaging microscopy; FP: fluorescence protein; FRET: Förster's resonance energy transfer; GABARAP: GABA type A receptor-associated protein; HBSS: Hanks' balanced salt solution; KO: knockout; LAMP2: lysosomal associated membrane protein 2; MAP1LC3/LC3: microtubule associated protein 1 light chain 3; NSC: NSC 185058; PE: phosphatidylethanolamine; SKO: single knockout; TKO: triple knockout; ULK1: unc-51 like autophagy activating kinase 1; WT: wild-type; ZPCK: Z-L-phe chloromethyl ketone.

Keywords: ATG4B; FRET-FLIM; LC3B; autophagy; biosensor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Autophagy* / genetics
  • Autophagy-Related Proteins / metabolism
  • Biosensing Techniques*
  • Fluorescence Resonance Energy Transfer / methods
  • Microtubule-Associated Proteins / metabolism

Substances

  • Autophagy-Related Proteins
  • Microtubule-Associated Proteins

Grants and funding

This work was supported by the Centre National de la Recherche Scientifique (CNRS), the University of Rennes 1, the Ligue Contre le Cancer Comité d’Ille et Vilaine et du Finistère and the Association pour la Recherche sur le Cancer (ARC) to G.B., and by the Institut National du Cancer (INCa) and ITMO Cancer/Aviesan to M.T. E.B.G. was supported by a fellowship from the Ligue Contre le Cancer and Région Bretagne (Brittany region, France).