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A proteomic network approach across the ALS-FTD disease spectrum resolves clinical phenotypes and genetic vulnerability in human brain.采用蛋白质组学网络方法对 ALS-FTD 疾病谱进行研究,可解析人脑的临床表型和遗传易感性。
EMBO Mol Med. 2018 Jan;10(1):48-62. doi: 10.15252/emmm.201708202.
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Regulator of G protein signaling 14 (RGS14) is expressed pre- and postsynaptically in neurons of hippocampus, basal ganglia, and amygdala of monkey and human brain.G 蛋白信号调节因子 14(RGS14)在猴脑和人脑的海马体、基底神经节和杏仁核的神经元中均有表达,既有突触前表达,也有突触后表达。
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Changes in the detergent-insoluble brain proteome linked to amyloid and tau in Alzheimer's Disease progression.与阿尔茨海默病进展过程中淀粉样蛋白和tau蛋白相关的去污剂不溶性脑蛋白质组的变化。
Proteomics. 2016 Dec;16(23):3042-3053. doi: 10.1002/pmic.201600057.
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The Perseus computational platform for comprehensive analysis of (prote)omics data.Perseus 计算平台,用于全面分析(蛋白质组学)数据。
Nat Methods. 2016 Sep;13(9):731-40. doi: 10.1038/nmeth.3901. Epub 2016 Jun 27.
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Rediscovering area CA2: unique properties and functions.重新发现CA2区:独特的特性和功能。
Nat Rev Neurosci. 2016 Feb;17(2):89-102. doi: 10.1038/nrn.2015.22.
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Social and novel contexts modify hippocampal CA2 representations of space.社交和新奇环境会改变海马体CA2区域对空间的表征。
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2016 update of the PRIDE database and its related tools.PRIDE数据库及其相关工具的2016年更新。
Nucleic Acids Res. 2016 Jan 4;44(D1):D447-56. doi: 10.1093/nar/gkv1145. Epub 2015 Nov 2.
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Regulator of G Protein Signaling 14: A Molecular Brake on Synaptic Plasticity Linked to Learning and Memory.G蛋白信号调节因子14:与学习和记忆相关的突触可塑性的分子制动器
Prog Mol Biol Transl Sci. 2015;133:169-206. doi: 10.1016/bs.pmbts.2015.03.006. Epub 2015 Apr 27.
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Integration of G protein α (Gα) signaling by the regulator of G protein signaling 14 (RGS14).G蛋白信号调节因子14(RGS14)对G蛋白α亚基(Gα)信号的整合作用
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Accurate proteome-wide label-free quantification by delayed normalization and maximal peptide ratio extraction, termed MaxLFQ.通过延迟归一化和最大肽段比率提取进行全蛋白质组精确的无标记定量,称为MaxLFQ。
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相互作用组分析揭示 G 蛋白信号调节因子 14(RGS14)是一种新型的钙/钙调蛋白(Ca/CaM)和钙调蛋白激酶 II(CaMKII)结合伴侣。

Interactome Analysis Reveals Regulator of G Protein Signaling 14 (RGS14) is a Novel Calcium/Calmodulin (Ca/CaM) and CaM Kinase II (CaMKII) Binding Partner.

机构信息

Department of Molecular Medicine , The Scripps Research Institute , Jupiter , Florida 33458 , United States.

Neurobiology Laboratory , National Institute of Environmental Health Sciences, National Institutes of Health , Research Triangle Park , North Carolina 27709 , United States.

出版信息

J Proteome Res. 2018 Apr 6;17(4):1700-1711. doi: 10.1021/acs.jproteome.8b00027. Epub 2018 Mar 20.

DOI:10.1021/acs.jproteome.8b00027
PMID:29518331
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6554723/
Abstract

Regulator of G Protein Signaling 14 (RGS14) is a complex scaffolding protein that integrates G protein and MAPK signaling pathways. In the adult mouse brain, RGS14 is predominantly expressed in hippocampal CA2 neurons where it naturally inhibits synaptic plasticity and hippocampus-dependent learning and memory. However, the signaling proteins that RGS14 natively engages to regulate plasticity are unknown. Here, we show that RGS14 exists in a high-molecular-weight protein complex in brain. To identify RGS14 neuronal interacting partners, endogenous RGS14 immunoprecipitated from mouse brain was subjected to mass spectrometry and proteomic analysis. We find that RGS14 interacts with key postsynaptic proteins that regulate plasticity. Gene ontology analysis reveals the most enriched RGS14 interactors have functional roles in actin-binding, calmodulin(CaM)-binding, and CaM-dependent protein kinase (CaMK) activity. We validate these findings using biochemical assays that identify interactions with two previously unknown binding partners. We report that RGS14 directly interacts with Ca/CaM and is phosphorylated by CaMKII in vitro. Lastly, we detect that RGS14 associates with CaMKII and CaM in hippocampal CA2 neurons. Taken together, these findings demonstrate that RGS14 is a novel CaM effector and CaMKII phosphorylation substrate thereby providing new insight into mechanisms by which RGS14 controls plasticity in CA2 neurons.

摘要

G 蛋白信号调节因子 14(RGS14)是一种复杂的支架蛋白,可整合 G 蛋白和 MAPK 信号通路。在成年小鼠大脑中,RGS14 主要表达在海马 CA2 神经元中,在这些神经元中,它自然抑制突触可塑性和海马依赖性学习和记忆。然而,RGS14 天然结合以调节可塑性的信号蛋白尚不清楚。在这里,我们表明 RGS14 存在于大脑中的高分子量蛋白质复合物中。为了鉴定 RGS14 的神经元相互作用伙伴,从小鼠脑中免疫沉淀的内源性 RGS14 进行了质谱和蛋白质组学分析。我们发现 RGS14 与调节可塑性的关键突触后蛋白相互作用。GO 分析显示,最丰富的 RGS14 相互作用物在肌动蛋白结合、钙调蛋白(CaM)结合和 CaM 依赖性蛋白激酶(CaMK)活性中具有功能作用。我们使用生化测定验证了这些发现,这些测定鉴定了与两个以前未知的结合伙伴的相互作用。我们报告 RGS14 直接与 Ca/CaM 相互作用,并在体外被 CaMKII 磷酸化。最后,我们在海马 CA2 神经元中检测到 RGS14 与 CaMKII 和 CaM 相关。总之,这些发现表明 RGS14 是一种新型的 CaM 效应物和 CaMKII 磷酸化底物,从而为 RGS14 控制 CA2 神经元可塑性的机制提供了新的见解。