Identification of Synaptic DGKθ Interactors That Stimulate DGKθ Activity.

IF 2.8 4区 医学 Q2 NEUROSCIENCES
Casey N Barber, Hana L Goldschmidt, Qianqian Ma, Lauren R Devine, Robert N Cole, Richard L Huganir, Daniel M Raben
{"title":"Identification of Synaptic DGKθ Interactors That Stimulate DGKθ Activity.","authors":"Casey N Barber,&nbsp;Hana L Goldschmidt,&nbsp;Qianqian Ma,&nbsp;Lauren R Devine,&nbsp;Robert N Cole,&nbsp;Richard L Huganir,&nbsp;Daniel M Raben","doi":"10.3389/fnsyn.2022.855673","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":12650,"journal":{"name":"Frontiers in Synaptic Neuroscience","volume":"14 ","pages":"855673"},"PeriodicalIF":2.8000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9095502/pdf/","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in Synaptic Neuroscience","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3389/fnsyn.2022.855673","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 1

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.

Abstract Image

Abstract Image

Abstract Image

刺激DGKθ活性的突触DGKθ相互作用物的鉴定。
脂质及其代谢酶是突触囊泡循环过程中诱导膜融合所需的膜曲率调节的关键点。一种这样的酶是二酰基甘油激酶θ (DGKθ),它产生磷脂酸(PtdOH),产生负的膜曲率。缺乏DGKθ的突触内吞速率明显较慢,暗示DGKθ是内吞调节因子。重要的是,DGKθ激酶活性是该功能所必需的。然而,神经元中DGKθ激酶活性的蛋白调节因子从未被发现。在这项研究中,我们采用APEX2接近标记和质谱技术鉴定了神经元中DGKθ的内源性相互作用物,并分析了它们调节DGKθ激酶活性的能力。鉴定出7种内源性DGKθ相互作用物,其中synaptotagmin-1 (Syt1)使DGKθ激酶活性增加10倍。这项研究首次验证了哺乳动物突触中的内源性DGKθ相互作用,并表明DGKθ产生的PtdOH和Syt1在突触囊泡循环中具有协调作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
7.10
自引率
2.70%
发文量
74
审稿时长
14 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信