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Identification of Synaptic DGKθ Interactors That Stimulate DGKθ Activity.
Barber, Casey N; Goldschmidt, Hana L; Ma, Qianqian; Devine, Lauren R; Cole, Robert N; Huganir, Richard L; Raben, Daniel M.
Afiliação
  • Barber CN; Department of Biological Chemistry, Johns Hopkins University School of Medicine, Baltimore, MD, United States.
  • Goldschmidt HL; Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD, United States.
  • Ma Q; Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD, United States.
  • Devine LR; Department of Biological Chemistry, Johns Hopkins University School of Medicine, Baltimore, MD, United States.
  • Cole RN; Department of Biological Chemistry, Johns Hopkins University School of Medicine, Baltimore, MD, United States.
  • Huganir RL; Department of Biological Chemistry, Johns Hopkins University School of Medicine, Baltimore, MD, United States.
  • Raben DM; Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD, United States.
Front Synaptic Neurosci ; 14: 855673, 2022.
Article em En | MEDLINE | ID: mdl-35573662
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Revista: Front Synaptic Neurosci Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Revista: Front Synaptic Neurosci Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos