4.8 Article

Accumulation of undegraded autophagosomes by expression of dominant-negative STX17 (syntaxin 17) mutants

Journal

AUTOPHAGY
Volume 13, Issue 8, Pages 1452-1464

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1080/15548627.2017.1327940

Keywords

autophagosome; fusion; lysosome; SNARE; syntaxin 17

Categories

Funding

  1. Japan Society for the Promotion of Science KAKENHI [26711011]
  2. MEXT [25111005]
  3. Japan Foundation for Applied Enzymology
  4. Government Subsidies for Management Expense of the University of Tokyo Medical Scientist Training Program
  5. Grants-in-Aid for Scientific Research [16K14720, 17H03670, 25111005, 26711011] Funding Source: KAKEN

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Macroautophagy/autophagy, which is one of the main degradation systems in the cell, is mediated by a specialized organelle, the autophagosome. Purification of autophagosomes before fusion with lysosomes is important for both mechanistic and physiological studies of the autophagosome. Here, we report a simple method to accumulate undigested autophagosomes. Overexpression of the autophagosomal Qa-SNARE STX17 (syntaxin 17) lacking the N-terminal domain (NTD) or N-terminally tagged GFP-STX17 causes accumulation of autophagosomes. A HeLa cell line, which expresses GFP-STX17DNTD or full-length GFP-STX17 under the control of the tetracycline-responsive promoter, accumulates a large number of undigested autophagosomes devoid of lysosomal markers or early autophagy factors upon treatment with doxycycline. Using this inducible cell line, nascent autophagosomes can be easily purified by OptiPrep density-gradient centrifugation and immunoprecipitation. This novel method should be useful for further characterization of nascent autophagosomes.

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