• 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

相似文献

1
The roles of Pol and Env in the assembly pathway of human foamy virus.多聚酶(Pol)和包膜蛋白(Env)在人泡沫病毒装配途径中的作用。
J Virol. 1998 May;72(5):3658-65. doi: 10.1128/JVI.72.5.3658-3665.1998.
2
Proteolytic activity, the carboxy terminus of Gag, and the primer binding site are not required for Pol incorporation into foamy virus particles.蛋白酶活性、Gag的羧基末端和引物结合位点对于Pol整合到泡沫病毒颗粒中不是必需的。
J Virol. 1999 Aug;73(8):6387-93. doi: 10.1128/JVI.73.8.6387-6393.1999.
3
Human foamy virus replication: a pathway distinct from that of retroviruses and hepadnaviruses.人泡沫病毒复制:一条不同于逆转录病毒和嗜肝DNA病毒的途径。
Science. 1996 Mar 15;271(5255):1579-82. doi: 10.1126/science.271.5255.1579.
4
Particle assembly and genome packaging.颗粒组装与基因组包装。
Curr Top Microbiol Immunol. 2003;277:89-110. doi: 10.1007/978-3-642-55701-9_4.
5
RNA and protein requirements for incorporation of the Pol protein into foamy virus particles.将Pol蛋白整合到泡沫病毒颗粒中所需的RNA和蛋白质
J Virol. 2005 Jun;79(11):7005-13. doi: 10.1128/JVI.79.11.7005-7013.2005.
6
Relationship of the env genes and the endonuclease domain of the pol genes of simian foamy virus type 1 and human foamy virus.猴泡沫病毒1型和人泡沫病毒的env基因与pol基因的核酸内切酶结构域之间的关系
J Virol. 1990 Jan;64(1):406-10. doi: 10.1128/JVI.64.1.406-410.1990.
7
Foamy virus assembly with emphasis on pol encapsidation.泡沫病毒组装,重点是聚合酶包裹。
Viruses. 2013 Mar 20;5(3):886-900. doi: 10.3390/v5030886.
8
Protein composition and morphology of human foamy virus intracellular cores and extracellular particles.人类泡沫病毒细胞内核心及细胞外颗粒的蛋白质组成与形态
Virology. 1997 Feb 17;228(2):307-17. doi: 10.1006/viro.1996.8379.
9
Proteolytic processing of foamy virus Gag and Pol proteins.泡沫病毒群Gag和Pol蛋白的蛋白水解加工
Curr Top Microbiol Immunol. 2003;277:63-88. doi: 10.1007/978-3-642-55701-9_3.
10
Mutagenesis of N-terminal residues of feline foamy virus Gag reveals entirely distinct functions during capsid formation, particle assembly, Gag processing and budding.猫泡沫病毒Gag蛋白N端残基的诱变揭示了衣壳形成、病毒粒子组装、Gag加工和出芽过程中完全不同的功能。
Retrovirology. 2016 Aug 22;13(1):57. doi: 10.1186/s12977-016-0291-8.

引用本文的文献

1
Efficient production of inhibitor-free foamy virus glycoprotein-containing retroviral vectors by proteoglycan-deficient packaging cells.通过蛋白聚糖缺陷型包装细胞高效生产不含抑制剂的含泡沫病毒糖蛋白的逆转录病毒载体。
Mol Ther Methods Clin Dev. 2022 Aug 1;26:394-412. doi: 10.1016/j.omtm.2022.07.004. eCollection 2022 Sep 8.
2
Plasma antibodies from humans infected with zoonotic simian foamy virus do not inhibit cell-to-cell transmission of the virus despite binding to the surface of infected cells.尽管与人感染的动物源性猴泡沫病毒结合,但来自感染人类的血浆抗体并不能抑制病毒的细胞间传播。
PLoS Pathog. 2022 May 23;18(5):e1010470. doi: 10.1371/journal.ppat.1010470. eCollection 2022 May.
3
Crystal Structure of a Retroviral Polyprotein: Prototype Foamy Virus Protease-Reverse Transcriptase (PR-RT).逆转录病毒多蛋白晶体结构:泡沫病毒蛋白酶-逆转录酶(PR-RT)原型。
Viruses. 2021 Jul 29;13(8):1495. doi: 10.3390/v13081495.
4
The Unique, the Known, and the Unknown of Spumaretrovirus Assembly.泡沫反转录病毒组装的独特性、已知性和未知性。
Viruses. 2021 Jan 13;13(1):105. doi: 10.3390/v13010105.
5
Foamy Virus Protein-Nucleic Acid Interactions during Particle Morphogenesis.泡沫病毒颗粒形态发生过程中的蛋白质-核酸相互作用
Viruses. 2016 Aug 30;8(9):243. doi: 10.3390/v8090243.
6
The cooperative function of arginine residues in the Prototype Foamy Virus Gag C-terminus mediates viral and cellular RNA encapsidation.原型泡沫病毒Gag C末端中精氨酸残基的协同作用介导病毒和细胞RNA的包裹。
Retrovirology. 2014 Oct 8;11:87. doi: 10.1186/s12977-014-0087-7.
7
New World simian foamy virus infections in vivo and in vitro.新型世界灵长类泡沫病毒的体内和体外感染。
J Virol. 2014 Jan;88(2):982-91. doi: 10.1128/JVI.03154-13. Epub 2013 Nov 6.
8
An N-terminal domain helical motif of Prototype Foamy Virus Gag with dual functions essential for particle egress and viral infectivity.原型泡沫病毒 Gag 蛋白 N 端结构域螺旋模体具有双重功能,对于粒子出芽和病毒感染力至关重要。
Retrovirology. 2013 Apr 25;10:45. doi: 10.1186/1742-4690-10-45.
9
Foamy virus budding and release.泡沫病毒出芽和释放。
Viruses. 2013 Apr 10;5(4):1075-98. doi: 10.3390/v5041075.
10
Foamy virus assembly with emphasis on pol encapsidation.泡沫病毒组装,重点是聚合酶包裹。
Viruses. 2013 Mar 20;5(3):886-900. doi: 10.3390/v5030886.

本文引用的文献

1
Evidence that the human foamy virus genome is DNA.人类泡沫病毒基因组为DNA的证据。
J Virol. 1999 Feb;73(2):1565-72. doi: 10.1128/JVI.73.2.1565-1572.1999.
2
Plasma membrane targeting of chimeric intracisternal A-type particle polyproteins leads to particle release and specific activation of the viral proteinase.嵌合的A型核内池颗粒多聚蛋白靶向质膜会导致颗粒释放和病毒蛋白酶的特异性激活。
J Virol. 1997 Jul;71(7):5209-17. doi: 10.1128/JVI.71.7.5209-5217.1997.
3
Characterization of human foamy virus proteins expressed by recombinant vaccinia viruses.重组痘苗病毒表达的人泡沫病毒蛋白的特性分析
AIDS Res Hum Retroviruses. 1997 Apr 10;13(6):517-21. doi: 10.1089/aid.1997.13.517.
4
A sorting motif localizes the foamy virus glycoprotein to the endoplasmic reticulum.一个分选基序将泡沫病毒糖蛋白定位于内质网。
J Virol. 1997 Jan;71(1):778-84. doi: 10.1128/JVI.71.1.778-784.1997.
5
Direct interaction between the envelope and matrix proteins of HIV-1.HIV-1包膜蛋白与基质蛋白之间的直接相互作用。
EMBO J. 1996 Nov 1;15(21):5783-8.
6
Human immunodeficiency virus type 2 glycoprotein enhancement of particle budding: role of the cytoplasmic domain.2型人类免疫缺陷病毒糖蛋白对病毒颗粒出芽的增强作用:胞质结构域的作用
J Virol. 1996 Apr;70(4):2669-73. doi: 10.1128/JVI.70.4.2669-2673.1996.
7
Foamy virus reverse transcriptase is expressed independently from the Gag protein.泡沫病毒逆转录酶独立于 gag 蛋白表达。
Proc Natl Acad Sci U S A. 1996 Apr 30;93(9):4137-41. doi: 10.1073/pnas.93.9.4137.
8
Human foamy virus replication: a pathway distinct from that of retroviruses and hepadnaviruses.人泡沫病毒复制:一条不同于逆转录病毒和嗜肝DNA病毒的途径。
Science. 1996 Mar 15;271(5255):1579-82. doi: 10.1126/science.271.5255.1579.
9
The envelope glycoprotein of human immunodeficiency virus type 2 enhances viral particle release: a Vpu-like factor?人类免疫缺陷病毒2型的包膜糖蛋白增强病毒颗粒释放:一种类似Vpu的因子?
J Virol. 1996 Feb;70(2):820-9. doi: 10.1128/JVI.70.2.820-829.1996.
10
The human foamy virus pol gene is expressed as a Pro-Pol polyprotein and not as a Gag-Pol fusion protein.人类泡沫病毒pol基因表达为前体多聚蛋白Pro-Pol,而非Gag-Pol融合蛋白。
J Virol. 1996 Feb;70(2):1033-40. doi: 10.1128/JVI.70.2.1033-1040.1996.

多聚酶(Pol)和包膜蛋白(Env)在人泡沫病毒装配途径中的作用。

The roles of Pol and Env in the assembly pathway of human foamy virus.

作者信息

Baldwin D N, Linial M L

机构信息

Division of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington 98104, USA.

出版信息

J Virol. 1998 May;72(5):3658-65. doi: 10.1128/JVI.72.5.3658-3665.1998.

DOI:10.1128/JVI.72.5.3658-3665.1998
PMID:9557646
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC109586/
Abstract

Human foamy virus (HFV) is the prototype of the Spumavirus genus of retroviruses. These viruses have a genomic organization close to that of other complex retroviruses but have similarities to hepadnaviruses such as human hepatitis B virus (HBV). Both HFV and HBV express their Pol protein independently of their structural proteins. Retroviruses and hepadnaviruses differ in their requirements for particle assembly and genome packaging. Assembly of retroviral particles containing RNA genomes requires only the Gag structural protein. The Pol protein is not required for capsid assembly, and the Env surface glycoprotein is not required for release of virions from the cell. In contrast, assembly of extracellular HBV particles containing DNA requires core structural protein and polymerase (P protein) for assembly of nucleocapsids and requires surface glycoproteins for release from the cell. We investigated the requirements for synthesis of extracellular HFV particles by constructing mutants with either the pol or env gene deleted. We found that the Pol protein is dispensable for production of extracellular particles containing viral nucleic acid. In the absence of Env, intracellular particles are synthesized but few or no extracellular particles could be detected. Thus, foamy virus assembly is distinct from that of other reverse transcriptase-encoding mammalian viruses.

摘要

人类泡沫病毒(HFV)是逆转录病毒泡沫病毒属的原型。这些病毒的基因组结构与其他复杂逆转录病毒相近,但与嗜肝DNA病毒如人类乙型肝炎病毒(HBV)有相似之处。HFV和HBV均独立于其结构蛋白表达其Pol蛋白。逆转录病毒和嗜肝DNA病毒在病毒颗粒组装和基因组包装的需求方面存在差异。含有RNA基因组的逆转录病毒颗粒的组装仅需要Gag结构蛋白。衣壳组装不需要Pol蛋白,并且病毒粒子从细胞中释放也不需要Env表面糖蛋白。相比之下,含有DNA的细胞外HBV颗粒的组装需要核心结构蛋白和聚合酶(P蛋白)来组装核衣壳,并且需要表面糖蛋白从细胞中释放。我们通过构建缺失pol或env基因的突变体来研究细胞外HFV颗粒合成的需求。我们发现,Pol蛋白对于产生含有病毒核酸的细胞外颗粒是可有可无的。在没有Env的情况下,会合成细胞内颗粒,但几乎检测不到或无法检测到细胞外颗粒。因此,泡沫病毒的组装与其他编码逆转录酶的哺乳动物病毒不同。