• 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

糖基磷脂酰肌醇-磷脂酶D:一种用于糖基磷脂酰肌醇结构分析的工具。

Glycosylphosphatidylinositol-phospholipase D: a tool for glycosylphosphatidylinositol structural analysis.

作者信息

Deeg M A, Davitz M A

机构信息

Department of Medicine, University of Washington, Seattle 98195, USA.

出版信息

Methods Enzymol. 1995;250:630-40. doi: 10.1016/0076-6879(95)50101-0.

DOI:10.1016/0076-6879(95)50101-0
PMID:7651182
Abstract

Cleavage by the GPI-PLD provides definitive evidence of a minimal GPI structure: glucosamine-phosphatidylinositol. Unlike the case for PI-PLC, cleavage by the GPI-PLD is unaffected by acylation of the inositol ring. Thus the GPI-PLD provides an excellent simple enzymatic tool for analyzing the basic core structure of GPI anchors.

摘要

糖基磷脂酰肌醇特异性磷脂酶D(GPI-PLD)的切割提供了关于最小GPI结构(葡糖胺-磷脂酰肌醇)的确切证据。与磷脂酰肌醇特异性磷脂酶C(PI-PLC)的情况不同,GPI-PLD的切割不受肌醇环酰化的影响。因此,GPI-PLD为分析GPI锚定物的基本核心结构提供了一种出色且简单的酶学工具。

相似文献

1
Glycosylphosphatidylinositol-phospholipase D: a tool for glycosylphosphatidylinositol structural analysis.糖基磷脂酰肌醇-磷脂酶D:一种用于糖基磷脂酰肌醇结构分析的工具。
Methods Enzymol. 1995;250:630-40. doi: 10.1016/0076-6879(95)50101-0.
2
Glycosylphosphatidylinositol-specific phospholipase D.
Methods Enzymol. 1991;197:567-75. doi: 10.1016/0076-6879(91)97184-z.
3
Purification and characterization of glycosyl-phosphatidylinositol-specific phospholipase D.
J Biol Chem. 1990 Oct 15;265(29):17738-45.
4
Characterization of the plasma glycosylphosphatidylinositol-specific phospholipase D (GPI-PLD).
Cell Biol Int Rep. 1991 Sep;15(9):875-82. doi: 10.1016/0309-1651(91)90039-l.
5
Crystal structure of phosphatidylinositol-specific phospholipase C from Bacillus cereus in complex with glucosaminyl(alpha 1-->6)-D-myo-inositol, an essential fragment of GPI anchors.蜡样芽孢杆菌磷脂酰肌醇特异性磷脂酶C与GPI锚定物的必需片段氨基葡萄糖基(α1→6)-D-肌醇复合物的晶体结构
Biochemistry. 1996 Jul 23;35(29):9496-504. doi: 10.1021/bi9606105.
6
Purification and characterization of human immunodeficiency virus type 1 reverse transcriptase.
Methods Enzymol. 1995;262:130-44. doi: 10.1016/0076-6879(95)62015-x.
7
Posttranslational modification of glycosylphosphatidylinositol (GPI)-specific phospholipase D and its activity in cleavage of GPI anchors.糖基磷脂酰肌醇(GPI)特异性磷脂酶D的翻译后修饰及其在切割GPI锚中的活性。
Biochem Biophys Res Commun. 1998 Oct 29;251(3):737-43. doi: 10.1006/bbrc.1998.9542.
8
Structural analysis of glycosylphosphatidylinositol anchors.糖基磷脂酰肌醇锚定物的结构分析
Methods Enzymol. 1994;230:418-42. doi: 10.1016/0076-6879(94)30027-5.
9
Factors affecting the ability of glycosylphosphatidylinositol-specific phospholipase D to degrade the membrane anchors of cell surface proteins.影响糖基磷脂酰肌醇特异性磷脂酶D降解细胞表面蛋白膜锚定物能力的因素。
Biochem J. 1991 Oct 15;279 ( Pt 2)(Pt 2):483-93. doi: 10.1042/bj2790483.
10
Alcohol dehydrogenase from Sulfolobus solfataricus.来自嗜热栖热菌的乙醇脱氢酶。
Methods Enzymol. 2001;331:176-95. doi: 10.1016/s0076-6879(01)31056-x.

引用本文的文献

1
Emerging connections between GPI-anchored proteins and their extracellular carriers in colorectal cancer.结直肠癌中糖基磷脂酰肌醇锚定蛋白与其细胞外载体之间新出现的联系。
Extracell Vesicles Circ Nucl Acids. 2023 Jun;4(2):195-217. doi: 10.20517/evcna.2023.17. Epub 2023 May 18.
2
Mass spectrometry-based detection and assignment of protein posttranslational modifications.基于质谱法的蛋白质翻译后修饰检测与鉴定
ACS Chem Biol. 2015 Jan 16;10(1):63-71. doi: 10.1021/cb500904b.
3
PGAP2 is essential for correct processing and stable expression of GPI-anchored proteins.
PGAP2对于糖基磷脂酰肌醇(GPI)锚定蛋白的正确加工和稳定表达至关重要。
Mol Biol Cell. 2006 Mar;17(3):1410-20. doi: 10.1091/mbc.e05-11-1005. Epub 2006 Jan 11.
4
Intracellular cleavage of glycosylphosphatidylinositol by phospholipase D induces activation of protein kinase Calpha.磷脂酶D对糖基磷脂酰肌醇的细胞内切割可诱导蛋白激酶Cα的激活。
Biochem J. 1999 Sep 1;342 ( Pt 2)(Pt 2):449-55.