刺激DGKθ活性的突触DGKθ相互作用物的鉴定。

IF 2.8 4区 医学 Q2 NEUROSCIENCES Frontiers in Synaptic Neuroscience Pub Date : 2022-01-01 DOI:10.3389/fnsyn.2022.855673
Casey N Barber, Hana L Goldschmidt, Qianqian Ma, Lauren R Devine, Robert N Cole, Richard L Huganir, Daniel M Raben
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引用次数: 1

摘要

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。
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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 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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来源期刊
CiteScore
7.10
自引率
2.70%
发文量
74
审稿时长
14 weeks
期刊最新文献
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