• 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

O-连接的N-乙酰葡糖胺(O-GlcNAc)与O-磷酸之间的动态相互作用:蛋白质调控的甜蜜一面。

Dynamic interplay between O-GlcNAc and O-phosphate: the sweet side of protein regulation.

作者信息

Slawson Chad, Hart Gerald W

机构信息

Department of Biological Chemistry, Johns Hopkins University School of Medicine, Baltimore, MD 21205-2185, USA.

出版信息

Curr Opin Struct Biol. 2003 Oct;13(5):631-6. doi: 10.1016/j.sbi.2003.08.003.

DOI:10.1016/j.sbi.2003.08.003
PMID:14568619
Abstract

Beta-O-linked N-acetylglucosamine (O-GlcNAc) is an abundant modification of cytosolic and nuclear proteins that occurs in metazoans. O-GlcNAc is dynamically processed by a unique set of enzymes that actively add and remove the modification. Functionally, O-GlcNAc appears to regulate protein stability, subcellular localization and protein-protein interactions. The modification often acts in a reciprocal manner to O-phosphate modifications of proteins and together they can synergistically control the activity of many cellular processes. Recently, O-GlcNAc has been demonstrated to play a significant role in diseases such as diabetes, cancer and neurodegeneration. For example, the increased levels of O-GlcNAc that occur in diabetes are associated with decreased insulin responsiveness in adipocytes.

摘要

β - O - 连接的N - 乙酰葡糖胺(O - GlcNAc)是后生动物中胞质和核蛋白丰富的修饰形式。O - GlcNAc由一组独特的酶动态加工,这些酶可主动添加和去除该修饰。在功能上,O - GlcNAc似乎调节蛋白质稳定性、亚细胞定位和蛋白质 - 蛋白质相互作用。这种修饰通常与蛋白质的O - 磷酸化修饰相互作用,二者共同协同控制许多细胞过程的活性。最近,已证明O - GlcNAc在糖尿病、癌症和神经退行性疾病等病症中起重要作用。例如,糖尿病中出现的O - GlcNAc水平升高与脂肪细胞中胰岛素反应性降低有关。

相似文献

1
Dynamic interplay between O-GlcNAc and O-phosphate: the sweet side of protein regulation.O-连接的N-乙酰葡糖胺(O-GlcNAc)与O-磷酸之间的动态相互作用:蛋白质调控的甜蜜一面。
Curr Opin Struct Biol. 2003 Oct;13(5):631-6. doi: 10.1016/j.sbi.2003.08.003.
2
O-GlcNAc: a regulatory post-translational modification.O-连接的N-乙酰葡糖胺:一种翻译后修饰调控方式
Biochem Biophys Res Commun. 2003 Mar 14;302(3):435-41. doi: 10.1016/s0006-291x(03)00175-x.
3
Cycling of O-linked beta-N-acetylglucosamine on nucleocytoplasmic proteins.核质蛋白上O-连接的β-N-乙酰葡糖胺循环
Nature. 2007 Apr 26;446(7139):1017-22. doi: 10.1038/nature05815.
4
[Role of O-GlcNAc modification of cellular proteins in signal transduction].[细胞蛋白的O-连接N-乙酰葡糖胺修饰在信号转导中的作用]
Postepy Biochem. 2007;53(4):389-99.
5
O-GlcNAc turns twenty: functional implications for post-translational modification of nuclear and cytosolic proteins with a sugar.O-连接的N-乙酰葡糖胺迎来二十岁:糖基化对核蛋白和胞质蛋白翻译后修饰的功能影响
FEBS Lett. 2003 Jul 3;546(1):154-8. doi: 10.1016/s0014-5793(03)00641-0.
6
O-GlcNAc a sensor of cellular state: the role of nucleocytoplasmic glycosylation in modulating cellular function in response to nutrition and stress.O-连接的N-乙酰葡糖胺——细胞状态的传感器:核质糖基化在响应营养和应激调节细胞功能中的作用
Biochim Biophys Acta. 2004 Jul 6;1673(1-2):13-28. doi: 10.1016/j.bbagen.2004.03.016.
7
Modulation of transcription factor function by O-GlcNAc modification.O-连接的N-乙酰葡糖胺修饰对转录因子功能的调控
Biochim Biophys Acta. 2010 May-Jun;1799(5-6):353-64. doi: 10.1016/j.bbagrm.2010.02.005. Epub 2010 Mar 2.
8
Tools for probing and perturbing O-GlcNAc in cells and in vivo.用于在细胞和体内探测和扰动 O-GlcNAc 的工具。
Curr Opin Chem Biol. 2013 Oct;17(5):719-28. doi: 10.1016/j.cbpa.2013.06.030. Epub 2013 Jul 30.
9
Detection and analysis of (O-linked beta-N-acetylglucosamine)-modified proteins.(O-连接的β-N-乙酰葡糖胺)修饰蛋白的检测与分析
Methods Mol Biol. 2009;464:227-54. doi: 10.1007/978-1-60327-461-6_13.
10
A Sweet Embrace: Control of Protein-Protein Interactions by O-Linked β-N-Acetylglucosamine.甜蜜的拥抱:O-连接的β-N-乙酰葡糖胺对蛋白质-蛋白质相互作用的调控
Biochemistry. 2018 Jan 9;57(1):13-21. doi: 10.1021/acs.biochem.7b00871. Epub 2017 Nov 20.

引用本文的文献

1
The β-1,4 GalT-V Interactome-Potential Therapeutic Targets and a Network of Pathways Driving Cancer and Cardiovascular and Inflammatory Diseases.β-1,4半乳糖基转移酶-V相互作用组——潜在治疗靶点以及驱动癌症、心血管疾病和炎症性疾病的信号通路网络
Int J Mol Sci. 2025 Aug 21;26(16):8088. doi: 10.3390/ijms26168088.
2
Enhancing protein O-GlcNAcylation in down syndrome mice mitigates memory dysfunctions through the rescue of mitochondrial bioenergetics, stress responses and pathological markers.增强唐氏综合征小鼠的蛋白质O-连接N-乙酰葡糖胺化可通过挽救线粒体生物能量学、应激反应和病理标志物来减轻记忆功能障碍。
Redox Biol. 2025 Jul 16;85:103769. doi: 10.1016/j.redox.2025.103769.
3
Hexosamine biosynthesis and related pathways, protein N-glycosylation and O-GlcNAcylation: their interconnection and role in plants.
己糖胺生物合成及相关途径、蛋白质N-糖基化和O-连接的N-乙酰葡糖胺化:它们在植物中的相互联系及作用
Front Plant Sci. 2024 Mar 6;15:1349064. doi: 10.3389/fpls.2024.1349064. eCollection 2024.
4
Protein O-GlcNAcylation and the regulation of energy homeostasis: lessons from knock-out mouse models.蛋白质 O-连接的 N-乙酰葡萄糖胺化与能量稳态调控:敲除小鼠模型的启示。
J Biomed Sci. 2022 Sep 4;29(1):64. doi: 10.1186/s12929-022-00851-w.
5
Effect of MACC1 Genetic Polymorphisms and Environmental Risk Factors in the Occurrence of Oral Squamous Cell Carcinoma.MACC1基因多态性及环境危险因素在口腔鳞状细胞癌发生中的作用
J Pers Med. 2021 May 31;11(6):490. doi: 10.3390/jpm11060490.
6
The Dysregulation of OGT/OGA Cycle Mediates Tau and APP Neuropathology in Down Syndrome.OGT/OGA 循环失调介导唐氏综合征中的 Tau 和 APP 神经病理学。
Neurotherapeutics. 2021 Jan;18(1):340-363. doi: 10.1007/s13311-020-00978-4. Epub 2020 Nov 30.
7
Mass spectrometry for the identification and analysis of highly complex glycosylation of therapeutic or pathogenic proteins.质谱法用于鉴定和分析治疗性或致病性蛋白质的高度复杂糖基化。
Expert Rev Proteomics. 2020 Apr;17(4):275-296. doi: 10.1080/14789450.2020.1769479. Epub 2020 May 28.
8
Neurofilament levels in patients with neurological diseases: A comparison of neurofilament light and heavy chain levels.神经丝在神经系统疾病患者中的水平:神经丝轻链和重链水平的比较。
J Clin Lab Anal. 2019 Sep;33(7):e22948. doi: 10.1002/jcla.22948. Epub 2019 Jun 14.
9
Protein Glycosylation and Tumor Microenvironment Alterations Driving Cancer Hallmarks.蛋白质糖基化与肿瘤微环境改变驱动癌症特征
Front Oncol. 2019 May 14;9:380. doi: 10.3389/fonc.2019.00380. eCollection 2019.
10
dbPTM in 2019: exploring disease association and cross-talk of post-translational modifications.dbPTM 于 2019 年:探索翻译后修饰的疾病关联和串扰。
Nucleic Acids Res. 2019 Jan 8;47(D1):D298-D308. doi: 10.1093/nar/gky1074.