• 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

使用荧光标记焦点在全细胞中同时测量 p53:Mdm2 和 p53:Mdm4 蛋白-蛋白相互作用。

Simultaneous measurement of p53:Mdm2 and p53:Mdm4 protein-protein interactions in whole cells using fluorescence labelled foci.

机构信息

p53 Laboratory, A*STAR (Agency for Science, Technology and Research), 8A Biomedical Grove, #06-04/05, Neuros/Immunos, Singapore, 138648, Singapore.

R&D Division, Medical & Biological Laboratories, Co., Ltd., 1063-103 Terasawaoka, Ina, Nagano, 396-0002, Japan.

出版信息

Sci Rep. 2019 Nov 29;9(1):17933. doi: 10.1038/s41598-019-54123-z.

DOI:10.1038/s41598-019-54123-z
PMID:31784573
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6884555/
Abstract

In this report we describe the development of a Fluorescent Protein-Protein Interaction-visualization (FLUOPPI) to enable the simultaneous measurement of both Mdm2:p53 and Mdm4:p53 interactions in order to assess the relative efficiencies of mimetic molecules of the p53 peptide helix against both PPIs. Mdm2 and Mdm4 overexpression frequently leads to the inactivation of non-mutated p53 in human cancers, via inhibition of its transcriptional activity, enhancing its degradation by the proteasome or by preventing its nuclear import. Development of inhibitors to disrupt the binding of one or both of these protein interactions have been the subject of intensive pharmaceutical development for anti-cancer therapies. Using the bimodal FLUOPPI system we have characterised compounds that were either monospecific for Mdm2 or bispecific for both Mdm2 and Mdm4. We have also demonstrated that the FLUOPPI assay can reliably differentiate between specific and non-specific disruption of these protein complexes via accurate assessment and normalization to the cell population under measurement. We envision that this methodology will increase the efficiency of identifying compounds that are either specific against a single PPI from a closely related family of interactions or compounds that interact across multiple related PPI pairs, depending on which is more desirable.

摘要

在本报告中,我们描述了荧光蛋白-蛋白相互作用可视化(FLUOPPI)的开发,以实现同时测量 Mdm2:p53 和 Mdm4:p53 相互作用,从而评估针对这两种 PPI 的 p53 肽螺旋模拟分子的相对效率。Mdm2 和 Mdm4 的过度表达经常通过抑制其转录活性、增强其通过蛋白酶体的降解或阻止其核输入来使非突变型 p53在人类癌症中失活。开发抑制剂以破坏这两种蛋白相互作用之一或两者的结合一直是癌症治疗的药物开发的重点。使用双模态 FLUOPPI 系统,我们已经对单特异性针对 Mdm2 的化合物或对 Mdm2 和 Mdm4 都具有双特异性的化合物进行了表征。我们还证明,FLUOPPI 测定法可以通过准确评估和对测量下的细胞群体进行归一化,可靠地区分这些蛋白复合物的特异性和非特异性破坏。我们设想这种方法将提高识别针对密切相关的相互作用家族中的单个 PPI 具有特异性的化合物或与多个相关 PPI 对相互作用的化合物的效率,具体取决于哪种方法更可取。

相似文献

1
Simultaneous measurement of p53:Mdm2 and p53:Mdm4 protein-protein interactions in whole cells using fluorescence labelled foci.使用荧光标记焦点在全细胞中同时测量 p53:Mdm2 和 p53:Mdm4 蛋白-蛋白相互作用。
Sci Rep. 2019 Nov 29;9(1):17933. doi: 10.1038/s41598-019-54123-z.
2
The fluorescent two-hybrid assay to screen for protein-protein interaction inhibitors in live cells: targeting the interaction of p53 with Mdm2 and Mdm4.用于在活细胞中筛选蛋白质-蛋白质相互作用抑制剂的荧光双杂交检测法:靶向p53与Mdm2和Mdm4的相互作用
J Biomol Screen. 2014 Apr;19(4):516-25. doi: 10.1177/1087057113518067. Epub 2014 Jan 29.
3
Discovery of MDM2-p53 and MDM4-p53 protein-protein interactions small molecule dual inhibitors.发现 MDM2-p53 和 MDM4-p53 蛋白-蛋白相互作用小分子双重抑制剂。
Eur J Med Chem. 2022 Nov 5;241:114637. doi: 10.1016/j.ejmech.2022.114637. Epub 2022 Aug 5.
4
MDM2 and MDM4: p53 regulators as targets in anticancer therapy.MDM2与MDM4:作为抗癌治疗靶点的p53调节因子
Int J Biochem Cell Biol. 2007;39(7-8):1476-82. doi: 10.1016/j.biocel.2007.03.022. Epub 2007 Apr 8.
5
Targeting the MDM2/MDM4 interaction interface as a promising approach for p53 reactivation therapy.针对 MDM2/MDM4 相互作用界面作为一种有前途的 p53 再激活治疗方法。
Cancer Res. 2015 Nov 1;75(21):4560-72. doi: 10.1158/0008-5472.CAN-15-0439. Epub 2015 Sep 10.
6
Lithocholic acid is an endogenous inhibitor of MDM4 and MDM2.胆酸是 MDM4 和 MDM2 的内源性抑制剂。
Proc Natl Acad Sci U S A. 2012 Oct 16;109(42):16906-10. doi: 10.1073/pnas.1215060109. Epub 2012 Oct 3.
7
Mdm2 Splice isoforms regulate the p53/Mdm2/Mdm4 regulatory circuit via RING domain-mediated ubiquitination of p53 and Mdm4.Mdm2剪接异构体通过RING结构域介导的p53和Mdm4泛素化来调节p53/Mdm2/Mdm4调控回路。
Cell Cycle. 2017 Apr 3;16(7):660-664. doi: 10.1080/15384101.2017.1288327. Epub 2017 Feb 6.
8
The long and the short of it: the MDM4 tail so far.长话短说:迄今为止的 MDM4 尾巴。
J Mol Cell Biol. 2019 Mar 1;11(3):231-244. doi: 10.1093/jmcb/mjz007.
9
α-Helix-Mimicking Sulfono-γ-AApeptide Inhibitors for p53-MDM2/MDMX Protein-Protein Interactions.α-螺旋模拟磺酰基-γ-AA 肽抑制剂用于 p53-MDM2/MDMX 蛋白-蛋白相互作用。
J Med Chem. 2020 Feb 13;63(3):975-986. doi: 10.1021/acs.jmedchem.9b00993. Epub 2020 Feb 3.
10
Multiplex detection of protein-protein interactions using a next generation luciferase reporter.使用新一代荧光素酶报告基因对蛋白质-蛋白质相互作用进行多重检测。
Biochim Biophys Acta. 2016 Feb;1863(2):284-92. doi: 10.1016/j.bbamcr.2015.11.031. Epub 2015 Nov 28.

引用本文的文献

1
Functional display of bioactive peptides on the vGFP scaffold.在 vGFP 支架上展示生物活性肽的功能。
Sci Rep. 2021 May 12;11(1):10127. doi: 10.1038/s41598-021-89421-y.

本文引用的文献

1
Monitoring flux in signalling pathways through measurements of 4EBP1-mediated eIF4F complex assembly.通过监测 4EBP1 介导的 eIF4F 复合物组装来监测信号通路中的通量。
BMC Biol. 2019 May 22;17(1):40. doi: 10.1186/s12915-019-0658-0.
2
Understanding Cell Penetration of Cyclic Peptides.理解环状肽的细胞穿透性。
Chem Rev. 2019 Sep 11;119(17):10241-10287. doi: 10.1021/acs.chemrev.9b00008. Epub 2019 May 14.
3
Targeted Intracellular Delivery of Antibodies: The State of the Art.抗体的靶向细胞内递送:现状
Front Pharmacol. 2018 Oct 24;9:1208. doi: 10.3389/fphar.2018.01208. eCollection 2018.
4
Inhibitors of protein-protein interactions (PPIs): an analysis of scaffold choices and buried surface area.蛋白质-蛋白质相互作用(PPIs)抑制剂:支架选择和埋藏表面积分析。
Curr Opin Chem Biol. 2018 Jun;44:75-86. doi: 10.1016/j.cbpa.2018.06.004. Epub 2018 Jun 13.
5
Dual inhibition of MDMX and MDM2 as a therapeutic strategy in leukemia.双重抑制 MDMX 和 MDM2 作为白血病的治疗策略。
Sci Transl Med. 2018 Apr 11;10(436). doi: 10.1126/scitranslmed.aao3003.
6
A quantitative comparison of cytosolic delivery via different protein uptake systems.不同蛋白摄取系统胞质内递送的定量比较。
Sci Rep. 2017 Oct 16;7(1):13194. doi: 10.1038/s41598-017-13469-y.
7
Strategies for transitioning macrocyclic peptides to cell-permeable drug leads.将大环肽转化为细胞渗透药物先导的策略。
Curr Opin Biotechnol. 2017 Dec;48:242-250. doi: 10.1016/j.copbio.2017.07.007. Epub 2017 Aug 5.
8
Enhancing Specific Disruption of Intracellular Protein Complexes by Hydrocarbon Stapled Peptides Using Lipid Based Delivery.通过基于脂质的递送来增强烃 stapled 肽对细胞内蛋白质复合物的特异性破坏。
Sci Rep. 2017 May 11;7(1):1763. doi: 10.1038/s41598-017-01712-5.
9
Genetic visualization of protein interactions harnessing liquid phase transitions.利用液相转变进行蛋白质相互作用的遗传可视化。
Sci Rep. 2017 Apr 13;7:46380. doi: 10.1038/srep46380.
10
The Roles of MDM2 and MDMX in Cancer.MDM2和MDMX在癌症中的作用。
Annu Rev Pathol. 2016 May 23;11:617-44. doi: 10.1146/annurev-pathol-012414-040349. Epub 2016 Mar 17.