• 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
Kinome profiling: A veritable Rosetta Stone for protease-activated receptor 1 biased signaling.激酶组分析:蛋白酶激活受体1偏向性信号传导的真正罗塞塔石碑。
Vascul Pharmacol. 2025 Mar;158:107469. doi: 10.1016/j.vph.2025.107469. Epub 2025 Feb 2.
2
Occupancy of human EPCR by protein C induces β-arrestin-2 biased PAR1 signaling by both APC and thrombin.蛋白C占据人内皮蛋白C受体可通过活化蛋白C和凝血酶诱导β-抑制蛋白2偏向性蛋白酶激活受体1信号传导。
Blood. 2016 Oct 6;128(14):1884-1893. doi: 10.1182/blood-2016-06-720581. Epub 2016 Aug 25.
3
Molecular basis for activation and biased signaling at the thrombin-activated GPCR proteinase activated receptor-4 (PAR4).血栓激活的 G 蛋白偶联受体蛋白酶激活受体-4(PAR4)的激活和偏向信号转导的分子基础。
J Biol Chem. 2020 Feb 21;295(8):2520-2540. doi: 10.1074/jbc.RA119.011461. Epub 2019 Dec 31.
4
Paradigm of Biased PAR1 (Protease-Activated Receptor-1) Activation and Inhibition in Endothelial Cells Dissected by Phosphoproteomics.通过磷酸化蛋白质组学剖析内皮细胞中偏向性PAR1(蛋白酶激活受体1)激活与抑制的范式
Arterioscler Thromb Vasc Biol. 2017 Oct;37(10):1891-1902. doi: 10.1161/ATVBAHA.117.309926. Epub 2017 Aug 17.
5
Neutrophil elastase and proteinase-3 trigger G protein-biased signaling through proteinase-activated receptor-1 (PAR1).中性粒细胞弹性蛋白酶和蛋白酶-3 通过蛋白酶激活受体-1(PAR1)触发 G 蛋白偏向性信号传导。
J Biol Chem. 2013 Nov 15;288(46):32979-90. doi: 10.1074/jbc.M113.483123. Epub 2013 Sep 19.
6
Phosphoproteomic analysis of protease-activated receptor-1 biased signaling reveals unique modulators of endothelial barrier function.磷酸化蛋白质组学分析揭示了蛋白酶激活受体-1 偏向信号传导的内皮屏障功能的独特调节剂。
Proc Natl Acad Sci U S A. 2020 Mar 3;117(9):5039-5048. doi: 10.1073/pnas.1917295117. Epub 2020 Feb 18.
7
G protein-coupled receptor kinase-5 regulates thrombin-activated signaling in endothelial cells.G蛋白偶联受体激酶-5调节内皮细胞中凝血酶激活的信号传导。
Proc Natl Acad Sci U S A. 2000 Jun 20;97(13):7440-5. doi: 10.1073/pnas.97.13.7440.
8
Caveolae are required for protease-selective signaling by protease-activated receptor-1.小窝对于蛋白酶激活受体-1介导的蛋白酶选择性信号传导是必需的。
Proc Natl Acad Sci U S A. 2009 Apr 14;106(15):6393-7. doi: 10.1073/pnas.0810687106. Epub 2009 Mar 30.
9
Acetaminophen Overdose Reveals PAR4 as a Low-Expressing but Potent Receptor on the Hepatic Endothelium in Mice.对乙酰氨基酚过量揭示PAR4是小鼠肝内皮细胞上一种低表达但强效的受体。
Arterioscler Thromb Vasc Biol. 2025 Jan;45(1):53-71. doi: 10.1161/ATVBAHA.124.321353. Epub 2024 Oct 3.
10
Biased agonism of protease-activated receptor-1 regulates thromboinflammation in murine sickle cell disease.蛋白酶激活受体-1 的偏性激动调节小鼠镰状细胞病中的血栓炎症。
Blood Adv. 2024 Jun 25;8(12):3272-3283. doi: 10.1182/bloodadvances.2023011907.

引用本文的文献

1
Novel Function for Endothelial Protease-Activated Receptors in Modulating Insulin Receptor Activity With Implications for Diabetes.内皮蛋白酶激活受体在调节胰岛素受体活性中的新功能及其对糖尿病的影响。
Arterioscler Thromb Vasc Biol. 2025 Jul 31. doi: 10.1161/ATVBAHA.125.323140.
2
A novel function for endothelial protease-activated receptors in modulating insulin receptor activity with implications for diabetes.内皮蛋白酶激活受体在调节胰岛素受体活性方面的新功能及其对糖尿病的影响。
bioRxiv. 2025 Mar 25:2025.03.21.644607. doi: 10.1101/2025.03.21.644607.

本文引用的文献

1
Endothelial protease-activated receptor 4: impotent or important?内皮蛋白酶激活受体4:无作用还是重要?
Front Cardiovasc Med. 2025 Jan 28;12:1541879. doi: 10.3389/fcvm.2025.1541879. eCollection 2025.
2
Acetaminophen Overdose Reveals PAR4 as a Low-Expressing but Potent Receptor on the Hepatic Endothelium in Mice.对乙酰氨基酚过量揭示PAR4是小鼠肝内皮细胞上一种低表达但强效的受体。
Arterioscler Thromb Vasc Biol. 2025 Jan;45(1):53-71. doi: 10.1161/ATVBAHA.124.321353. Epub 2024 Oct 3.
3
The intrinsic substrate specificity of the human tyrosine kinome.人类酪氨酸激酶组的固有底物特异性。
Nature. 2024 May;629(8014):1174-1181. doi: 10.1038/s41586-024-07407-y. Epub 2024 May 8.
4
An atlas of substrate specificities for the human serine/threonine kinome.人类丝氨酸/苏氨酸激酶组的底物特异性图谱
Nature. 2023 Jan;613(7945):759-766. doi: 10.1038/s41586-022-05575-3. Epub 2023 Jan 11.
5
A journey from phosphotyrosine to phosphohistidine and beyond.从磷酸酪氨酸到磷酸组氨酸的历程及超越。
Mol Cell. 2022 Jun 16;82(12):2190-2200. doi: 10.1016/j.molcel.2022.05.007. Epub 2022 Jun 1.
6
The AMPK-related kinase NUAK2 suppresses glutathione peroxidase 4 expression and promotes ferroptotic cell death in breast cancer cells.与AMPK相关的激酶NUAK2抑制谷胱甘肽过氧化物酶4的表达并促进乳腺癌细胞的铁死亡。
Cell Death Discov. 2022 May 6;8(1):253. doi: 10.1038/s41420-022-01044-y.
7
Phosphoproteomic analysis of protease-activated receptor-1 biased signaling reveals unique modulators of endothelial barrier function.磷酸化蛋白质组学分析揭示了蛋白酶激活受体-1 偏向信号传导的内皮屏障功能的独特调节剂。
Proc Natl Acad Sci U S A. 2020 Mar 3;117(9):5039-5048. doi: 10.1073/pnas.1917295117. Epub 2020 Feb 18.
8
IKKβ regulates essential functions of the vascular endothelium through kinase-dependent and -independent pathways.IKKβ 通过激酶依赖和非依赖途径调节血管内皮的基本功能。
Nat Commun. 2011;2:318. doi: 10.1038/ncomms1317.
9
Loss of neuroprotective survival signal in mice lacking insulin receptor gene in rod photoreceptor cells.在视杆光感受器细胞中缺乏胰岛素受体基因的小鼠中神经保护性生存信号的丧失。
J Biol Chem. 2008 Jul 11;283(28):19781-92. doi: 10.1074/jbc.M802374200. Epub 2008 May 14.

Kinome profiling: A veritable Rosetta Stone for protease-activated receptor 1 biased signaling.

作者信息

Rajala Rahul, Griffin Courtney T

机构信息

Cardiovascular Biology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, United States; Department of Cell Biology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, United States; Harold Hamm Diabetes Center, University of Oklahoma Health Sciences Center, Oklahoma City, OK, United States.

Cardiovascular Biology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, United States; Department of Cell Biology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, United States.

出版信息

Vascul Pharmacol. 2025 Mar;158:107469. doi: 10.1016/j.vph.2025.107469. Epub 2025 Feb 2.

DOI:10.1016/j.vph.2025.107469
PMID:39904417
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11890924/
Abstract
摘要