A photoconvertible fluorescent reporter to track chaperone-mediated autophagy

Hiroshi Koga, Marta Martinez-Vicente, Fernando Macian-Juan, Vladislav Verkhusha, Ana Maria Cuervo

Research output: Contribution to journalArticle

75 Citations (Scopus)

Abstract

Chaperone-mediated autophagy (CMA) is a selective mechanism for the degradation of soluble proteins in lysosomes. CMA contributes to cellular quality control and is activated as part of the cellular response to different stressors. Defective CMA has been identified in ageing and different age-related diseases. Until now, CMA activity could only be measured in vitro using isolated lysosomes. Here we report the development of a photoconvertible fluorescent reporter that allows monitoring of CMA activity in living cells. Activation of CMA increases the association of the reporter with lysosomes which can be visualized as a change in the intracellular fluorescence. The CMA reporter can be utilized in a broad variety of cells and is suitable for high-content microscopy. Using this reporter, we find that levels of basal and inducible CMA activity are cell-type dependent, and we have identified an upregulation of this pathway in response to the catalytic inhibition of the proteasome.

Original languageEnglish (US)
Article number386
JournalNature Communications
Volume2
Issue number1
DOIs
StatePublished - 2011

Fingerprint

lysosomes
Autophagy
Proteasome Endopeptidase Complex
Quality control
Microscopic examination
Aging of materials
Fluorescence
Chemical activation
Cells
Association reactions
Degradation
Monitoring
Proteins
Lysosomes
quality control
cells
activation
degradation
microscopy
proteins

ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)
  • Chemistry(all)
  • Physics and Astronomy(all)

Cite this

A photoconvertible fluorescent reporter to track chaperone-mediated autophagy. / Koga, Hiroshi; Martinez-Vicente, Marta; Macian-Juan, Fernando; Verkhusha, Vladislav; Cuervo, Ana Maria.

In: Nature Communications, Vol. 2, No. 1, 386, 2011.

Research output: Contribution to journalArticle

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