• 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

迈向N端拓扑生成蛋白序列的比较解剖学

Towards a comparative anatomy of N-terminal topogenic protein sequences.

作者信息

von Heijne G

出版信息

J Mol Biol. 1986 May 5;189(1):239-42. doi: 10.1016/0022-2836(86)90394-3.

DOI:10.1016/0022-2836(86)90394-3
PMID:3783674
Abstract

A comparative study of three kinds of eukaryotic N-terminal topogenic sequences, viz signal peptides, N-terminal transmembrane anchors, and mitochondrial targeting sequences, suggests: that the sign of the N-terminal charge might influence the orientation of an N-terminal hydrophobic segment relative to the membrane and give rise to N-terminally anchored proteins with their main mass exposed either on the cytosolic or extra-cytosolic side of the membrane; and that N-terminal transmembrane segments in mitochondrial targeting sequences have a relatively low overall hydrophobicity, probably in order to avoid being recognized by the endoplasmic reticulum export machinery.

摘要

对三种真核生物N端拓扑序列(即信号肽、N端跨膜锚定序列和线粒体靶向序列)的比较研究表明:N端电荷的正负可能影响N端疏水片段相对于膜的方向,从而产生N端锚定蛋白,其主要质量暴露在膜的胞质侧或胞外侧;线粒体靶向序列中的N端跨膜片段总体疏水性相对较低,这可能是为了避免被内质网输出机制识别。

相似文献

1
Towards a comparative anatomy of N-terminal topogenic protein sequences.迈向N端拓扑生成蛋白序列的比较解剖学
J Mol Biol. 1986 May 5;189(1):239-42. doi: 10.1016/0022-2836(86)90394-3.
2
An amphiphilic lipid-binding domain influences the topology of a signal-anchor sequence in the mitochondrial outer membrane.一个两亲性脂质结合结构域影响线粒体外膜中信号锚定序列的拓扑结构。
Biochemistry. 1996 Mar 26;35(12):3764-71. doi: 10.1021/bi9528053.
3
A signal-anchor sequence selective for the mitochondrial outer membrane.一种对线粒体外膜具有选择性的信号锚定序列。
J Cell Biol. 1992 Dec;119(6):1451-7. doi: 10.1083/jcb.119.6.1451.
4
Common principles of protein translocation across membranes.蛋白质跨膜转运的共同原则。
Science. 1996 Mar 15;271(5255):1519-26. doi: 10.1126/science.271.5255.1519.
5
Characterization of the signal that directs Tom20 to the mitochondrial outer membrane.引导Tom20定位于线粒体外膜的信号的特征分析。
J Cell Biol. 2000 Oct 16;151(2):277-88. doi: 10.1083/jcb.151.2.277.
6
The human mitochondrial import receptor, hTom20p, prevents a cryptic matrix targeting sequence from gaining access to the protein translocation machinery.人类线粒体输入受体hTom20p可阻止隐蔽的基质靶向序列接近蛋白质转运机制。
J Cell Biol. 1996 Jul;134(2):307-13. doi: 10.1083/jcb.134.2.307.
7
Functions of signal and signal-anchor sequences are determined by the balance between the hydrophobic segment and the N-terminal charge.信号序列和信号锚定序列的功能由疏水片段和N端电荷之间的平衡决定。
Proc Natl Acad Sci U S A. 1992 Jan 1;89(1):16-9. doi: 10.1073/pnas.89.1.16.
8
Novel targeting signals mediate the sorting of different isoforms of the tail-anchored membrane protein cytochrome b5 to either endoplasmic reticulum or mitochondria.新型靶向信号介导尾锚定膜蛋白细胞色素b5的不同异构体分选至内质网或线粒体。
Plant Cell. 2004 Nov;16(11):3002-19. doi: 10.1105/tpc.104.026039. Epub 2004 Oct 14.
9
The topogenic contribution of uncharged amino acids on signal sequence orientation in the endoplasmic reticulum.内质网中不带电荷氨基酸对信号序列取向的拓扑形成作用。
J Biol Chem. 2000 May 19;275(20):14916-22. doi: 10.1074/jbc.M000456200.
10
The membrane-interactive tail of cytochrome b(5) can function as a stop-transfer sequence in concert with a signal sequence to give inversion of protein topology in the endoplasmic reticulum.细胞色素b(5)的膜结合尾部可与信号序列协同作用,作为终止转移序列,使内质网中的蛋白质拓扑结构发生反转。
Arch Biochem Biophys. 2003 Apr 15;412(2):259-66. doi: 10.1016/s0003-9861(03)00051-1.

引用本文的文献

1
Signal Peptides and Their Fragments in Post-Translation: Novel Insights of Signal Peptides.翻译后修饰中的信号肽及其片段:信号肽的新见解
Int J Mol Sci. 2024 Dec 18;25(24):13534. doi: 10.3390/ijms252413534.
2
Signal peptide stabilizes folding and inhibits misfolding of serum amyloid A.信号肽稳定血清淀粉样蛋白 A 的折叠并抑制其错误折叠。
Protein Sci. 2022 Dec;31(12):e4485. doi: 10.1002/pro.4485.
3
Signal Peptide Features Determining the Substrate Specificities of Targeting and Translocation Components in Human ER Protein Import.
决定人类内质网蛋白质导入中靶向和转运成分底物特异性的信号肽特征
Front Physiol. 2022 Jul 11;13:833540. doi: 10.3389/fphys.2022.833540. eCollection 2022.
4
Signal Sequence-Dependent Orientation of Signal Peptide Fragments to Exosomes.信号序列依赖性的信号肽片段定向到外泌体。
Int J Mol Sci. 2022 Mar 15;23(6):3137. doi: 10.3390/ijms23063137.
5
The Molecular Biodiversity of Protein Targeting and Protein Transport Related to the Endoplasmic Reticulum.内质网相关的蛋白质靶向和蛋白质运输的分子生物多样性。
Int J Mol Sci. 2021 Dec 23;23(1):143. doi: 10.3390/ijms23010143.
6
Quantitative Proteomics and Differential Protein Abundance Analysis after Depletion of Putative mRNA Receptors in the ER Membrane of Human Cells Identifies Novel Aspects of mRNA Targeting to the ER.在人细胞内质网膜中假定的mRNA受体耗竭后进行定量蛋白质组学和差异蛋白质丰度分析,揭示了mRNA靶向内质网的新方面。
Molecules. 2021 Jun 11;26(12):3591. doi: 10.3390/molecules26123591.
7
Complexity and Specificity of Sec61-Channelopathies: Human Diseases Affecting Gating of the Sec61 Complex.Sec61 通道病的复杂性和特异性:影响 Sec61 复合物门控的人类疾病。
Cells. 2021 Apr 27;10(5):1036. doi: 10.3390/cells10051036.
8
Septal secretion of protein A in requires SecA and lipoteichoic acid synthesis.需要 SecA 和脂磷壁酸合成来实现蛋白 A 在 中的隔室分泌。
Elife. 2018 May 14;7:e34092. doi: 10.7554/eLife.34092.
9
Recombinant expression, purification and biochemical characterization of kievitone hydratase from Nectria haematococca.血座壳菌中基辅酮水合酶的重组表达、纯化及生化特性分析
PLoS One. 2018 Feb 8;13(2):e0192653. doi: 10.1371/journal.pone.0192653. eCollection 2018.
10
An Update on Sec61 Channel Functions, Mechanisms, and Related Diseases.Sec61通道的功能、机制及相关疾病的最新进展
Front Physiol. 2017 Nov 1;8:887. doi: 10.3389/fphys.2017.00887. eCollection 2017.