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Identification of Synaptic DGKθ Interactors That Stimulate DGKθ Activity

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 curvatur...

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Autores principales: Barber, Casey N., Goldschmidt, Hana L., Ma, Qianqian, Devine, Lauren R., Cole, Robert N., Huganir, Richard L., Raben, Daniel M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9095502/
https://www.ncbi.nlm.nih.gov/pubmed/35573662
http://dx.doi.org/10.3389/fnsyn.2022.855673
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author Barber, Casey N.
Goldschmidt, Hana L.
Ma, Qianqian
Devine, Lauren R.
Cole, Robert N.
Huganir, Richard L.
Raben, Daniel M.
author_facet Barber, Casey N.
Goldschmidt, Hana L.
Ma, Qianqian
Devine, Lauren R.
Cole, Robert N.
Huganir, Richard L.
Raben, Daniel M.
author_sort Barber, Casey N.
collection PubMed
description 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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spelling pubmed-90955022022-05-13 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. Front Synaptic Neurosci Synaptic Neuroscience 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. Frontiers Media S.A. 2022-04-27 /pmc/articles/PMC9095502/ /pubmed/35573662 http://dx.doi.org/10.3389/fnsyn.2022.855673 Text en Copyright © 2022 Barber, Goldschmidt, Ma, Devine, Cole, Huganir and Raben. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Synaptic Neuroscience
Barber, Casey N.
Goldschmidt, Hana L.
Ma, Qianqian
Devine, Lauren R.
Cole, Robert N.
Huganir, Richard L.
Raben, Daniel M.
Identification of Synaptic DGKθ Interactors That Stimulate DGKθ Activity
title Identification of Synaptic DGKθ Interactors That Stimulate DGKθ Activity
title_full Identification of Synaptic DGKθ Interactors That Stimulate DGKθ Activity
title_fullStr Identification of Synaptic DGKθ Interactors That Stimulate DGKθ Activity
title_full_unstemmed Identification of Synaptic DGKθ Interactors That Stimulate DGKθ Activity
title_short Identification of Synaptic DGKθ Interactors That Stimulate DGKθ Activity
title_sort identification of synaptic dgkθ interactors that stimulate dgkθ activity
topic Synaptic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9095502/
https://www.ncbi.nlm.nih.gov/pubmed/35573662
http://dx.doi.org/10.3389/fnsyn.2022.855673
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