Identification of Synaptic DGKθ Interactors That Stimulate DGKθ Activity

Casey N. Barber, Hana L. Goldschmidt, Qianqian Ma, Lauren R. Devine, Robert N. Cole, Richard L. Huganir, Daniel M. Raben

Research output: Contribution to journalArticlepeer-review

Abstract

Lipids and their metabolic enzymes are a critical point of regulation for the membrane curvature required to induce membrane fusion during synaptic vesicle recycling. One such enzyme is diacylglycerol kinase θ (DGKθ), which produces phosphatidic acid (PtdOH) that generates negative membrane curvature. Synapses lacking DGKθ have significantly slower rates of endocytosis, implicating DGKθ as an endocytic regulator. Importantly, DGKθ kinase activity is required for this function. However, protein regulators of DGKθ’s kinase activity in neurons have never been identified. In this study, we employed APEX2 proximity labeling and mass spectrometry to identify endogenous interactors of DGKθ in neurons and assayed their ability to modulate its kinase activity. Seven endogenous DGKθ interactors were identified and notably, synaptotagmin-1 (Syt1) increased DGKθ kinase activity 10-fold. This study is the first to validate endogenous DGKθ interactors at the mammalian synapse and suggests a coordinated role between DGKθ-produced PtdOH and Syt1 in synaptic vesicle recycling.

Original languageEnglish (US)
Article number855673
JournalFrontiers in Synaptic Neuroscience
Volume14
DOIs
StatePublished - Apr 27 2022

Keywords

  • APEX2
  • Syt1
  • lipids
  • neurotransmission
  • proximity labeling
  • synapse
  • synaptic vesicles

ASJC Scopus subject areas

  • Cellular and Molecular Neuroscience
  • Cell Biology

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