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Ypt1/RAB1 Identified as Trigger for Phagophore Expansion in Autophagy

Revealing how phagophore membranes draw lipids from the endoplasmic reticulum, this discovery opens avenues for targeted therapies against cancer, neurodegeneration, infection.

Overview

  • Aarhus University researchers pinpointed the GTPase Ypt1/RAB1 as the molecular switch that initiates phagophore expansion during autophagy.
  • Ypt1/RAB1 establishes a contact site with the endoplasmic reticulum to coordinate lipid transfer and membrane elongation of the phagophore.
  • The study appears in Nature Structural & Molecular Biology, confirming a long-sought regulatory step in the cellular waste-clearance pathway.
  • Modulating this mechanism could inform new treatments for diseases linked to autophagy dysfunction, including cancer, neurodegenerative disorders and infections.
  • Translating these mechanistic insights into therapies will require further investigation into safety and efficacy in disease models.