• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Proximity-dependent Proteomics Reveals Extensive Interactions of Protocadherin-19 with Regulators of Rho GTPases and the Microtubule Cytoskeleton.邻近依赖性蛋白质组学揭示原钙黏蛋白-19与Rho GTPases调节因子和微管细胞骨架的广泛相互作用。
Neuroscience. 2021 Jan 1;452:26-36. doi: 10.1016/j.neuroscience.2020.09.033. Epub 2020 Oct 1.
2
Structural determinants of adhesion by Protocadherin-19 and implications for its role in epilepsy.原钙黏蛋白 19 黏附的结构决定因素及其在癫痫中的作用。
Elife. 2016 Oct 26;5:e18529. doi: 10.7554/eLife.18529.
3
Proteomic analysis of the developing mammalian brain links PCDH19 to the Wnt/β-catenin signalling pathway.哺乳动物大脑发育过程中的蛋白质组学分析将 PCDH19 与 Wnt/β-catenin 信号通路联系起来。
Mol Psychiatry. 2024 Jul;29(7):2199-2210. doi: 10.1038/s41380-024-02482-z. Epub 2024 Mar 7.
4
A complete Protocadherin-19 ectodomain model for evaluating epilepsy-causing mutations and potential protein interaction sites.用于评估致癫痫突变和潜在蛋白质相互作用位点的完整原钙黏蛋白-19胞外域模型。
Structure. 2021 Oct 7;29(10):1128-1143.e4. doi: 10.1016/j.str.2021.07.006. Epub 2021 Sep 13.
5
Expanding the genetic and clinical characteristics of Protocadherin 19 gene mutations.拓展原钙黏蛋白 19 基因突变的遗传和临床特征。
BMC Med Genomics. 2022 Aug 17;15(1):181. doi: 10.1186/s12920-022-01313-w.
6
A complex of Protocadherin-19 and N-cadherin mediates a novel mechanism of cell adhesion.原钙黏蛋白 19 和 N 钙黏蛋白复合物介导细胞黏附的新机制。
J Cell Biol. 2011 Dec 26;195(7):1115-21. doi: 10.1083/jcb.201108115. Epub 2011 Dec 19.
7
Female-specific synaptic dysfunction and cognitive impairment in a mouse model of disorder.疾病小鼠模型中的雌性特异性突触功能障碍和认知障碍。
Science. 2021 Apr 16;372(6539). doi: 10.1126/science.aaz3893.
8
Mosaic and non-mosaic protocadherin 19 mutation leads to neuronal hyperexcitability in zebrafish.原钙黏蛋白 19 突变导致斑马鱼神经元过度兴奋。
Neurobiol Dis. 2022 Jul;169:105738. doi: 10.1016/j.nbd.2022.105738. Epub 2022 Apr 20.
9
Mapping combinatorial expression of non-clustered protocadherins in the developing brain identifies novel PCDH19-mediated cell adhesion properties.绘制未聚类原钙黏蛋白在发育中大脑中的组合表达图谱,确定新型 PCDH19 介导的细胞黏附特性。
Open Biol. 2024 Apr;14(4):230383. doi: 10.1098/rsob.230383. Epub 2024 Apr 17.
10
Multicenter retrospective study of patients with PCDH19-related epilepsy: The first Hungarian cohort.多中心回顾性研究:PCDH19 相关癫痫患者,匈牙利首例队列研究。
Epileptic Disord. 2024 Oct;26(5):685-693. doi: 10.1002/epd2.20264. Epub 2024 Jul 17.

引用本文的文献

1
Altered cytoskeleton dynamics in patient-derived iPSC-based model of PCDH19 clustering epilepsy.在基于患者诱导多能干细胞的原钙黏蛋白19簇集性癫痫模型中细胞骨架动力学改变。
Front Cell Dev Biol. 2025 Jan 6;12:1518533. doi: 10.3389/fcell.2024.1518533. eCollection 2024.
2
Proteomic analysis of the developing mammalian brain links PCDH19 to the Wnt/β-catenin signalling pathway.哺乳动物大脑发育过程中的蛋白质组学分析将 PCDH19 与 Wnt/β-catenin 信号通路联系起来。
Mol Psychiatry. 2024 Jul;29(7):2199-2210. doi: 10.1038/s41380-024-02482-z. Epub 2024 Mar 7.
3
PCDH9 suppresses melanoma proliferation and cell migration.原钙黏蛋白9抑制黑色素瘤的增殖和细胞迁移。
Front Oncol. 2022 Nov 14;12:903554. doi: 10.3389/fonc.2022.903554. eCollection 2022.
4
Modifying PCDH19 levels affects cortical interneuron migration.改变原钙黏蛋白19(PCDH19)的水平会影响皮质中间神经元的迁移。
Front Neurosci. 2022 Oct 25;16:887478. doi: 10.3389/fnins.2022.887478. eCollection 2022.
5
Modeling PCDH19-CE: From 2D Stem Cell Model to 3D Brain Organoids.建模 PCDH19-CE:从 2D 干细胞模型到 3D 脑类器官。
Int J Mol Sci. 2022 Mar 23;23(7):3506. doi: 10.3390/ijms23073506.
6
Right Place at the Right Time: How Changes in Protocadherins Affect Synaptic Connections Contributing to the Etiology of Neurodevelopmental Disorders.恰到好处的时机:原钙黏蛋白的变化如何影响突触连接,从而导致神经发育障碍的发病机制。
Cells. 2020 Dec 18;9(12):2711. doi: 10.3390/cells9122711.

本文引用的文献

1
Family-wide Structural and Biophysical Analysis of Binding Interactions among Non-clustered δ-Protocadherins.全家族结构与非簇集 δ-原钙黏蛋白结合相互作用的生物物理分析。
Cell Rep. 2020 Feb 25;30(8):2655-2671.e7. doi: 10.1016/j.celrep.2020.02.003.
2
Tuning of delta-protocadherin adhesion through combinatorial diversity.通过组合多样性来调节δ原钙黏蛋白的黏附。
Elife. 2018 Dec 14;7:e41050. doi: 10.7554/eLife.41050.
3
Homozygous PCDH12 variants result in phenotype of cerebellar ataxia, dystonia, retinopathy, and dysmorphism.纯合 PCDH12 变异导致小脑共济失调、肌张力障碍、视网膜病变和发育异常的表型。
J Hum Genet. 2019 Feb;64(2):183-189. doi: 10.1038/s10038-018-0541-9. Epub 2018 Nov 20.
4
Down-regulated of PCDH10 predicts poor prognosis in hepatocellular carcinoma patients.PCDH10表达下调预示着肝细胞癌患者预后不良。
Medicine (Baltimore). 2018 Aug;97(35):e12055. doi: 10.1097/MD.0000000000012055.
5
Protocadherin-8 promotes invasion and metastasis via laminin subunit γ2 in gastric cancer.原钙黏蛋白-8通过层粘连蛋白亚基γ2促进胃癌的侵袭和转移。
Cancer Sci. 2018 Mar;109(3):732-740. doi: 10.1111/cas.13502. Epub 2018 Feb 20.
6
Low Expression of Protocadherin-8 Promotes the Progression of Ovarian Cancer.原钙黏蛋白 8 低表达促进卵巢癌的进展。
Int J Gynecol Cancer. 2018 Feb;28(2):346-354. doi: 10.1097/IGC.0000000000001169.
7
PCDH8 inhibits glioma cell proliferation by negatively regulating the AKT/GSK3β/β-catenin signaling pathway.PCDH8通过负向调节AKT/GSK3β/β-连环蛋白信号通路抑制胶质瘤细胞增殖。
Oncol Lett. 2017 Sep;14(3):3357-3362. doi: 10.3892/ol.2017.6629. Epub 2017 Jul 20.
8
Association between protocadherin 8 promoter hypermethylation and the pathological status of prostate cancer.原钙黏蛋白8启动子高甲基化与前列腺癌病理状态之间的关联。
Oncol Lett. 2017 Aug;14(2):1657-1664. doi: 10.3892/ol.2017.6282. Epub 2017 May 31.
9
Structural determinants of adhesion by Protocadherin-19 and implications for its role in epilepsy.原钙黏蛋白 19 黏附的结构决定因素及其在癫痫中的作用。
Elife. 2016 Oct 26;5:e18529. doi: 10.7554/eLife.18529.
10
A chromosome 16p13.11 microduplication causes hyperactivity through dysregulation of miR-484/protocadherin-19 signaling.16号染色体p13.11微重复通过miR-484/原钙黏蛋白-19信号通路失调导致多动。
Mol Psychiatry. 2017 Mar;22(3):364-374. doi: 10.1038/mp.2016.106. Epub 2016 Jul 5.

邻近依赖性蛋白质组学揭示原钙黏蛋白-19与Rho GTPases调节因子和微管细胞骨架的广泛相互作用。

Proximity-dependent Proteomics Reveals Extensive Interactions of Protocadherin-19 with Regulators of Rho GTPases and the Microtubule Cytoskeleton.

作者信息

Emond Michelle R, Biswas Sayantanee, Morrow Matthew L, Jontes James D

机构信息

Department of Neuroscience, Ohio State University, United States.

Department of Neuroscience, Ohio State University, United States.

出版信息

Neuroscience. 2021 Jan 1;452:26-36. doi: 10.1016/j.neuroscience.2020.09.033. Epub 2020 Oct 1.

DOI:10.1016/j.neuroscience.2020.09.033
PMID:33010346
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7772771/
Abstract

Protocadherin-19 belongs to the cadherin family of cell surface receptors and has been shown to play essential roles in the development of the vertebrate nervous system. Mutations in human Protocadherin-19 (PCDH19) lead to PCDH19 Female-limited epilepsy (PCDH19 FLE) in humans, characterized by the early onset of epileptic seizures in children and a range of cognitive and behavioral problems in adults. Despite being considered the second most prevalent gene in epilepsy, very little is known about the intercellular pathways in which it participates. In order to characterize the protein complexes within which Pcdh19 functions, we generated Pcdh19-BioID fusion proteins and utilized proximity-dependent biotinylation to identify neighboring proteins. Proteomic identification and analysis revealed that the Pcdh19 interactome is enriched in proteins that regulate Rho family GTPases, microtubule binding proteins and proteins that regulate cell divisions. We cloned the centrosomal protein Nedd1 and the RacGEF Dock7 and verified their interactions with Pcdh19 in vitro. Our findings provide the first comprehensive insights into the interactome of Pcdh19, and provide a platform for future investigations into the cellular and molecular biology of this protein critical to the proper development of the nervous system.

摘要

原钙黏蛋白-19属于细胞表面受体的钙黏蛋白家族,已被证明在脊椎动物神经系统发育中发挥重要作用。人类原钙黏蛋白-19(PCDH19)的突变会导致人类PCDH19女性局限性癫痫(PCDH19 FLE),其特征为儿童期癫痫发作早发,以及成人期一系列认知和行为问题。尽管它被认为是癫痫中第二常见的基因,但对其参与的细胞间通路却知之甚少。为了表征Pcdh19发挥功能的蛋白质复合物,我们生成了Pcdh19-BioID融合蛋白,并利用邻近依赖性生物素化来识别邻近蛋白。蛋白质组学鉴定和分析表明,Pcdh19相互作用组富含调节Rho家族GTP酶的蛋白质、微管结合蛋白以及调节细胞分裂的蛋白质。我们克隆了中心体蛋白Nedd1和RacGEF Dock7,并在体外验证了它们与Pcdh19的相互作用。我们的研究结果首次全面深入了解了Pcdh19的相互作用组,并为未来研究这种对神经系统正常发育至关重要的蛋白质的细胞和分子生物学提供了一个平台。