• 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

Sec61介导的膜蛋白从内质网转移至蛋白酶体进行降解。

Sec61-mediated transfer of a membrane protein from the endoplasmic reticulum to the proteasome for destruction.

作者信息

Wiertz E J, Tortorella D, Bogyo M, Yu J, Mothes W, Jones T R, Rapoport T A, Ploegh H L

机构信息

Center for Cancer Research, Department of Biology, Massachusetts Institute of Technology, Cambridge 02139, USA.

出版信息

Nature. 1996 Dec 5;384(6608):432-8. doi: 10.1038/384432a0.

DOI:10.1038/384432a0
PMID:8945469
Abstract

The human cytomegalovirus genome encodes proteins that trigger destruction of newly synthesized major histocompatibility complex (MHC) class I molecules. The human cytomegalovirus gene US2 specifies a product capable of dislocating MHC class I molecules from the endoplasmic reticulum to the cytosol and delivering them to the proteasome. This process involves the Sec61 complex, in what appears to be a reversal of the reaction by which it translocates nascent chains into the endoplasmic reticulum.

摘要

人类巨细胞病毒基因组编码的蛋白质可引发新合成的主要组织相容性复合体(MHC)I类分子的破坏。人类巨细胞病毒基因US2编码的产物能够将MHC I类分子从内质网转运至细胞质溶胶,并将它们递送至蛋白酶体。这一过程涉及Sec61复合体,这似乎是其将新生肽链转运至内质网的反应的逆转。

相似文献

1
Sec61-mediated transfer of a membrane protein from the endoplasmic reticulum to the proteasome for destruction.Sec61介导的膜蛋白从内质网转移至蛋白酶体进行降解。
Nature. 1996 Dec 5;384(6608):432-8. doi: 10.1038/384432a0.
2
Reversal of fortune for nascent proteins.新生蛋白质的命运逆转。
Nature. 1996 Dec 5;384(6608):405-6. doi: 10.1038/384405a0.
3
Endoplasmic reticulum-associated protein degradation.内质网相关蛋白降解
Semin Cell Dev Biol. 2000 Jun;11(3):159-64. doi: 10.1006/scdb.2000.0160.
4
The human cytomegalovirus US11 gene product dislocates MHC class I heavy chains from the endoplasmic reticulum to the cytosol.人类巨细胞病毒US11基因产物将MHC I类重链从内质网转运至胞质溶胶。
Cell. 1996 Mar 8;84(5):769-79. doi: 10.1016/s0092-8674(00)81054-5.
5
The mechanism underlying cystic fibrosis transmembrane conductance regulator transport from the endoplasmic reticulum to the proteasome includes Sec61beta and a cytosolic, deglycosylated intermediary.囊性纤维化跨膜传导调节因子从内质网转运至蛋白酶体的潜在机制包括Sec61β和一种胞质去糖基化中间体。
J Biol Chem. 1998 Nov 6;273(45):29873-8. doi: 10.1074/jbc.273.45.29873.
6
Binding of human cytomegalovirus US2 to major histocompatibility complex class I and II proteins is not sufficient for their degradation.人类巨细胞病毒US2与主要组织相容性复合体I类和II类蛋白的结合并不足以使其降解。
J Virol. 2002 Aug;76(16):8265-75. doi: 10.1128/jvi.76.16.8265-8275.2002.
7
Ubiquitination is essential for human cytomegalovirus US11-mediated dislocation of MHC class I molecules from the endoplasmic reticulum to the cytosol.泛素化对于人巨细胞病毒US11介导的主要组织相容性复合体I类分子从内质网向内质网-胞质溶胶转运至关重要。
Biochem J. 2001 Sep 1;358(Pt 2):369-77. doi: 10.1042/0264-6021:3580369.
8
Retro-translocation of proteins from the endoplasmic reticulum into the cytosol.蛋白质从内质网逆向转运至细胞质溶胶。
Nat Rev Mol Cell Biol. 2002 Apr;3(4):246-55. doi: 10.1038/nrm780.
9
Retrotranslocation of MHC class I heavy chain from the endoplasmic reticulum to the cytosol is dependent on ATP supply to the ER lumen.主要组织相容性复合体I类重链从内质网到胞质溶胶的逆向转运依赖于内质网腔的ATP供应。
Mol Immunol. 2004 Jan;40(10):733-41. doi: 10.1016/j.molimm.2003.08.008.
10
The protein translocation channel mediates glycopeptide export across the endoplasmic reticulum membrane.蛋白质转运通道介导糖肽跨内质网膜输出。
Proc Natl Acad Sci U S A. 2000 Apr 25;97(9):4609-14. doi: 10.1073/pnas.090083497.

引用本文的文献

1
B4GALT5 inhibits CD8 T-cell response by downregulating MHC-I level through ERAD pathway in PDAC.B4GALT5通过内质网相关蛋白降解(ERAD)途径下调MHC-I水平,从而抑制胰腺导管腺癌(PDAC)中的CD8 T细胞反应。
J Immunother Cancer. 2025 May 2;13(5):e010908. doi: 10.1136/jitc-2024-010908.
2
Immune Shielding of Human Heart Valves: A Proof-of-Concept Study of HLA-Targeting Therapy for Transplantations.人类心脏瓣膜的免疫屏蔽:移植 HLA 靶向治疗的概念验证研究
JACC Basic Transl Sci. 2024 Sep 11;9(11):1345-1359. doi: 10.1016/j.jacbts.2024.07.003. eCollection 2024 Nov.
3
Regulation of the cell surface expression of classical and non-classical MHC proteins by the human cytomegalovirus UL40 and rhesus cytomegalovirus Rh67 proteins.
人巨细胞病毒 UL40 和恒河猴巨细胞病毒 Rh67 蛋白对经典和非经典 MHC 蛋白细胞表面表达的调节。
J Virol. 2024 Sep 17;98(9):e0120624. doi: 10.1128/jvi.01206-24. Epub 2024 Aug 29.
4
HCMV US2 co-opts TRC8 to degrade the endoplasmic reticulum-resident protein LMAN2L.HCMV US2 劫持 TRC8 以降解内质网驻留蛋白 LMAN2L。
J Gen Virol. 2024 Apr;105(4). doi: 10.1099/jgv.0.001980.
5
Diverse cytomegalovirus US11 antagonism and MHC-A evasion strategies reveal a tit-for-tat coevolutionary arms race in hominids.巨细胞病毒 US11 的多种拮抗作用和 MHC-A 逃逸策略揭示了人类中针锋相对的共同进化军备竞赛。
Proc Natl Acad Sci U S A. 2024 Feb 27;121(9):e2315985121. doi: 10.1073/pnas.2315985121. Epub 2024 Feb 20.
6
Controlling Antigen Fate in Therapeutic Cancer Vaccines by Targeting Dendritic Cell Receptors.通过靶向树突状细胞受体控制治疗性癌症疫苗中的抗原命运
Mol Pharm. 2023 Oct 2;20(10):4826-4847. doi: 10.1021/acs.molpharmaceut.3c00330. Epub 2023 Sep 18.
7
The Orf9b protein of SARS-CoV-2 modulates mitochondrial protein biogenesis.SARS-CoV-2 的 Orf9b 蛋白调节线粒体蛋白的生物发生。
J Cell Biol. 2023 Oct 2;222(10). doi: 10.1083/jcb.202303002. Epub 2023 Sep 8.
8
Mechanisms of substrate processing during ER-associated protein degradation.内质网相关蛋白降解过程中底物加工的机制。
Nat Rev Mol Cell Biol. 2023 Nov;24(11):777-796. doi: 10.1038/s41580-023-00633-8. Epub 2023 Aug 1.
9
Characteristics and Functions of HEV Proteins.戊型肝炎病毒蛋白的特性与功能。
Adv Exp Med Biol. 2023;1417:15-32. doi: 10.1007/978-981-99-1304-6_2.
10
Intracellular trafficking of HLA-E and its regulation.HLA-E 的细胞内转运及其调控。
J Exp Med. 2023 Aug 7;220(8). doi: 10.1084/jem.20221941. Epub 2023 May 4.