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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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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. |
format | Online Article Text |
id | pubmed-9095502 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
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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