• 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

肌醇磷酸与分离的普列克底物蛋白同源结构域的特异性高亲和力结合。

Specific and high-affinity binding of inositol phosphates to an isolated pleckstrin homology domain.

作者信息

Lemmon M A, Ferguson K M, O'Brien R, Sigler P B, Schlessinger J

机构信息

Department of Pharmacology, New York University Medical Center, New York 10016, USA.

出版信息

Proc Natl Acad Sci U S A. 1995 Nov 7;92(23):10472-6. doi: 10.1073/pnas.92.23.10472.

DOI:10.1073/pnas.92.23.10472
PMID:7479822
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC40633/
Abstract

Pleckstrin homology (PH) domains are found in many signaling molecules and are thought to be involved in specific intermolecular interactions. Their binding to several proteins and to membranes containing 1-alpha-phosphatidylinositol 4,5-bisphosphate [PtdIns(4,5)P2] has been reported. A region that includes the PH domain has also been implicated in binding of phospholipase C-delta 1 (PLC-delta 1) to both PtdIns(4,5)P2 and D-myo-inositol 1,4,5-trisphosphate [Ins(1,4,5)P3] [Cifuentes, M. E., Delaney, T. & Rebecchi, M. J. (1994) J. Biol. Chem. 269, 1945-1948]. We report herein that the isolated PH domain from PLC-delta 1 binds to both PtdIns(4,5)P2 and Ins(1,4,5)P3 with high affinity and shows the same binding specificity seen by others with whole PLC-delta 1. Thus the PH domain is functionally and structurally modular. These results demonstrate stereo-specific high-affinity binding by an isolated PH domain and further support a functional role for PH domains in the regulation of PLC isoforms. Other PH domains did not bind strongly to the compounds tested, suggesting that inositol phosphates and phospholipids are not likely physiological ligands for all PH domains. Nonetheless, since all PH-domain-containing proteins are associated with membrane surfaces, several PH domains bind to specific sites on membranes, and PH domains appear to be electrostatically polarized, a possible general role for PH domains in membrane association is suggested.

摘要

普列克底物蛋白同源(PH)结构域存在于许多信号分子中,被认为参与特定的分子间相互作用。据报道,它们能与多种蛋白质以及含有1-α-磷脂酰肌醇4,5-二磷酸[PtdIns(4,5)P2]的膜结合。包含PH结构域的一个区域也与磷脂酶C-δ1(PLC-δ1)结合PtdIns(4,5)P2和D-肌醇1,4,5-三磷酸[Ins(1,4,5)P3]有关[西富恩特斯,M.E.,德莱尼,T. & 雷贝奇,M.J.(1994年)《生物化学杂志》269卷,第1945 - 1948页]。我们在此报告,从PLC-δ1分离出的PH结构域能以高亲和力与PtdIns(4,5)P2和Ins(1,4,5)P3结合,并且表现出与其他人用完整PLC-δ1观察到的相同结合特异性。因此,PH结构域在功能和结构上是模块化的。这些结果证明了分离出的PH结构域具有立体特异性高亲和力结合,并进一步支持了PH结构域在调节PLC同工型中的功能作用。其他PH结构域与所测试的化合物结合不强,这表明肌醇磷酸酯和磷脂不太可能是所有PH结构域的生理配体。尽管如此,由于所有含PH结构域的蛋白质都与膜表面相关,一些PH结构域能与膜上的特定位点结合,并且PH结构域似乎是静电极化的,因此提示了PH结构域在膜结合中可能具有普遍作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd50/40633/e599df1c93ec/pnas01501-0039-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd50/40633/e599df1c93ec/pnas01501-0039-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd50/40633/e599df1c93ec/pnas01501-0039-a.jpg

相似文献

1
Specific and high-affinity binding of inositol phosphates to an isolated pleckstrin homology domain.肌醇磷酸与分离的普列克底物蛋白同源结构域的特异性高亲和力结合。
Proc Natl Acad Sci U S A. 1995 Nov 7;92(23):10472-6. doi: 10.1073/pnas.92.23.10472.
2
Involvement of EF hand motifs in the Ca(2+)-dependent binding of the pleckstrin homology domain to phosphoinositides.EF手基序参与pleckstrin同源结构域与磷酸肌醇的钙离子依赖性结合。
Eur J Biochem. 1999 Oct 1;265(1):481-90. doi: 10.1046/j.1432-1327.1999.00786.x.
3
Specificity and promiscuity in phosphoinositide binding by pleckstrin homology domains.普列克底物蛋白同源结构域在磷酸肌醇结合中的特异性与多效性
J Biol Chem. 1998 Nov 13;273(46):30497-508. doi: 10.1074/jbc.273.46.30497.
4
Replacements of single basic amino acids in the pleckstrin homology domain of phospholipase C-delta1 alter the ligand binding, phospholipase activity, and interaction with the plasma membrane.磷脂酶C-δ1的普列克底物蛋白同源结构域中单个碱性氨基酸的替换会改变配体结合、磷脂酶活性以及与质膜的相互作用。
J Biol Chem. 1998 Jan 2;273(1):417-24. doi: 10.1074/jbc.273.1.417.
5
Differential association of the pleckstrin homology domains of phospholipases C-beta 1, C-beta 2, and C-delta 1 with lipid bilayers and the beta gamma subunits of heterotrimeric G proteins.磷脂酶C-β1、C-β2和C-δ1的普列克底物蛋白同源结构域与脂质双层以及异源三聚体G蛋白的βγ亚基的差异关联。
Biochemistry. 1999 Feb 2;38(5):1517-24. doi: 10.1021/bi982008f.
6
D-myo-inositol 1,4,5-trisphosphate inhibits binding of phospholipase C-delta 1 to bilayer membranes.D-肌醇1,4,5-三磷酸抑制磷脂酶C-δ1与双层膜的结合。
J Biol Chem. 1994 Jan 21;269(3):1945-8.
7
Phosphoinositide binding specificity among phospholipase C isozymes as determined by photo-cross-linking to novel substrate and product analogs.通过与新型底物和产物类似物进行光交联确定的磷脂酶C同工酶之间的磷酸肌醇结合特异性。
Biochemistry. 1997 Jun 10;36(23):7239-48. doi: 10.1021/bi9702288.
8
Mutation in the pleckstrin homology domain of the human phospholipase C-delta 1 gene is associated with loss of function.人类磷脂酶C-δ1基因pleckstrin同源结构域的突变与功能丧失相关。
Biochem Biophys Res Commun. 1998 Apr 28;245(3):722-8. doi: 10.1006/bbrc.1998.8307.
9
A novel phospholipase C delta4 (PLCdelta4) splice variant as a negative regulator of PLC.一种新型磷脂酶Cδ4(PLCδ4)剪接变体作为磷脂酶C的负调节因子。
J Biol Chem. 1999 Jan 29;274(5):2872-9. doi: 10.1074/jbc.274.5.2872.
10
Localization of a high-affinity inositol 1,4,5-trisphosphate/inositol 1,4,5,6-tetrakisphosphate binding domain to the pleckstrin homology module of a new 130 kDa protein: characterization of the determinants of structural specificity.一种高亲和力的肌醇1,4,5-三磷酸/肌醇1,4,5,6-四磷酸结合结构域在一种新的130 kDa蛋白质的普列克底物蛋白同源模块中的定位:结构特异性决定因素的表征
Biochem J. 1996 Sep 1;318 ( Pt 2)(Pt 2):561-8. doi: 10.1042/bj3180561.

引用本文的文献

1
Nanoscale clustering and dynamics of phosphatidylinositol 4,5-bisphosphate in an immune cell model.免疫细胞模型中磷脂酰肌醇4,5-二磷酸的纳米级聚集与动力学
Biophys J. 2025 Jul 5. doi: 10.1016/j.bpj.2025.07.004.
2
Characterization of the malaria parasite Tepsin homolog.疟原虫Tepsin同源物的特性分析。
Microbiol Spectr. 2025 Aug 5;13(8):e0328824. doi: 10.1128/spectrum.03288-24. Epub 2025 Jun 30.
3
Nanodisc single-molecule pulldown to study lipid-protein interactions.利用纳米圆盘单分子下拉技术研究脂类-蛋白质相互作用。

本文引用的文献

1
Measurement of protein-binding phenomena by gel filtration.通过凝胶过滤法测定蛋白质结合现象。
Biochim Biophys Acta. 1962 Oct 8;63:530-2. doi: 10.1016/0006-3002(62)90124-5.
2
A putative modular domain present in diverse signaling proteins.一种存在于多种信号蛋白中的假定模块化结构域。
Cell. 1993 May 21;73(4):629-30. doi: 10.1016/0092-8674(93)90244-k.
3
Pleckstrin domain homology.普列克底物蛋白结构域同源性
J Lipid Res. 2025 Jul;66(7):100846. doi: 10.1016/j.jlr.2025.100846. Epub 2025 Jun 20.
4
The ascent of AKAPs, from architectural elements to kinase anchors: a perspective.A激酶锚定蛋白(AKAPs)的崛起:从结构元件到激酶锚定物的视角
Biochem J. 2025 May 13;482(10):BCJ20253085. doi: 10.1042/BCJ20253085.
5
Regulation of phosphatidylinositol-(4,5)-bisphosphate and active-Rho1p levels and distribution is crucial for correct spatio-temporal cytokinesis and echinocandin responses in .磷脂酰肌醇-(4,5)-二磷酸和活性Rho1p水平及分布的调节对于正确的时空胞质分裂和棘白菌素反应至关重要。
Antimicrob Agents Chemother. 2025 Jun 4;69(6):e0190024. doi: 10.1128/aac.01900-24. Epub 2025 May 5.
6
Nonvesicular cholesterol transport in physiology.生理学中的非囊泡性胆固醇转运
J Clin Invest. 2025 Mar 17;135(6):e188127. doi: 10.1172/JCI188127.
7
Probing and imaging phospholipid dynamics in live cells.探测和成像活细胞中的磷脂动力学。
Life Metab. 2024 Apr 13;3(4):loae014. doi: 10.1093/lifemeta/loae014. eCollection 2024 Aug.
8
Septin Organization and Dynamics for Budding Yeast Cytokinesis.芽殖酵母胞质分裂中的Septin蛋白组织与动态变化
J Fungi (Basel). 2024 Sep 9;10(9):642. doi: 10.3390/jof10090642.
9
MTM1-mediated production of phosphatidylinositol 5-phosphate fuels the formation of podosome-like protrusions regulating myoblast fusion.MTM1 介导的磷脂酰肌醇 5-磷酸的生成为形成类似于 Podosome 的突起提供燃料,从而调节成肌细胞融合。
Proc Natl Acad Sci U S A. 2024 Jun 4;121(23):e2217971121. doi: 10.1073/pnas.2217971121. Epub 2024 May 28.
10
Mitochondria-ER-PM contacts regulate mitochondrial division and PI(4)P distribution.线粒体-内质网-质膜接触调控线粒体分裂和 PI(4)P 分布。
J Cell Biol. 2024 Sep 2;223(9). doi: 10.1083/jcb.202308144. Epub 2024 May 23.
Nature. 1993 May 27;363(6427):309-10. doi: 10.1038/363309b0.
4
Identification of novel pleckstrin homology (PH) domains provides a hypothesis for PH domain function.新型普列克底物蛋白同源(PH)结构域的鉴定为PH结构域的功能提供了一种假设。
Biochem Biophys Res Commun. 1993 Sep 15;195(2):1145-51. doi: 10.1006/bbrc.1993.2164.
5
Identification of two regions of beta G spectrin that bind to distinct sites in brain membranes.鉴定βG血影蛋白与脑膜中不同位点结合的两个区域。
J Biol Chem. 1994 Feb 11;269(6):4409-16.
6
D-myo-inositol 1,4,5-trisphosphate inhibits binding of phospholipase C-delta 1 to bilayer membranes.D-肌醇1,4,5-三磷酸抑制磷脂酶C-δ1与双层膜的结合。
J Biol Chem. 1994 Jan 21;269(3):1945-8.
7
The PH domain: a common piece in the structural patchwork of signalling proteins.PH结构域:信号蛋白结构拼凑中的一个常见组成部分。
Trends Biochem Sci. 1993 Sep;18(9):343-8. doi: 10.1016/0968-0004(93)90071-t.
8
Structure of the pleckstrin homology domain from beta-spectrin.来自β-血影蛋白的普列克底物蛋白同源结构域的结构
Nature. 1994 Jun 23;369(6482):675-7. doi: 10.1038/369675a0.
9
Solution structure of a pleckstrin-homology domain.普列克底物蛋白同源结构域的溶液结构
Nature. 1994 Jun 23;369(6482):672-5. doi: 10.1038/369672a0.
10
PH domains and phospholipases--a meaningful relationship?PH结构域与磷脂酶——一种有意义的关系?
Trends Biochem Sci. 1994 Feb;19(2):54-5. doi: 10.1016/0968-0004(94)90031-0.