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非洲爪蟾卵母细胞中乙型肝炎表面抗原多肽细胞内运输和组装的障碍

A block to the intracellular transport and assembly of hepatitis B surface antigen polypeptides in Xenopus oocytes.

作者信息

Simon K, Lingappa V R, Ganem D

机构信息

Department of Microbiology, University of California Medical Center, San Francisco 94143.

出版信息

Virology. 1988 Sep;166(1):76-81. doi: 10.1016/0042-6822(88)90148-1.

DOI:10.1016/0042-6822(88)90148-1
PMID:3413987
Abstract

Hepatitis B surface antigen is the major protein of the virion envelope, and is also independently secreted from infected cells as a subviral particle composed exclusively of HBsAg and host-derived lipid. Similar particles are efficiently assembled and secreted by cultured mammalian cells transfected with the gene for HBsAg. In contrast to such cultured cells, Xenopus oocytes microinjected with HBsAg mRNA secrete less than 5% of newly synthesized HBsAg polypeptides. We have examined the HBsAg biosynthetic intermediates in such oocytes and provide evidence that the impaired secretion of HBsAg is due to a discrete block in the assembly of lipoprotein particles.

摘要

乙型肝炎表面抗原是病毒粒子包膜的主要蛋白质,也作为仅由乙肝表面抗原和宿主来源脂质组成的亚病毒颗粒从受感染细胞中独立分泌。用乙肝表面抗原基因转染的培养哺乳动物细胞能高效组装并分泌类似颗粒。与这种培养细胞不同,显微注射乙肝表面抗原信使核糖核酸的非洲爪蟾卵母细胞分泌的新合成乙肝表面抗原多肽不到5%。我们已研究了此类卵母细胞中乙肝表面抗原的生物合成中间体,并提供证据表明乙肝表面抗原分泌受损是由于脂蛋白颗粒组装过程中的一个离散阻滞。

相似文献

1
A block to the intracellular transport and assembly of hepatitis B surface antigen polypeptides in Xenopus oocytes.非洲爪蟾卵母细胞中乙型肝炎表面抗原多肽细胞内运输和组装的障碍
Virology. 1988 Sep;166(1):76-81. doi: 10.1016/0042-6822(88)90148-1.
2
Secreted hepatitis B surface antigen polypeptides are derived from a transmembrane precursor.分泌型乙肝表面抗原多肽源自一种跨膜前体。
J Cell Biol. 1988 Dec;107(6 Pt 1):2163-8. doi: 10.1083/jcb.107.6.2163.
3
Reduced secretion of virions and hepatitis B virus (HBV) surface antigen of a naturally occurring HBV variant correlates with the accumulation of the small S envelope protein in the endoplasmic reticulum and Golgi apparatus.一种自然发生的乙肝病毒(HBV)变体的病毒粒子和乙肝表面抗原分泌减少,这与小S包膜蛋白在内质网和高尔基体中的积累有关。
J Virol. 2005 Nov;79(21):13483-96. doi: 10.1128/JVI.79.21.13483-13496.2005.
4
Assembly of viral particles in Xenopus oocytes: pre-surface-antigens regulate secretion of the hepatitis B viral surface envelope particle.非洲爪蟾卵母细胞中病毒颗粒的组装:前表面抗原调节乙型肝炎病毒表面包膜颗粒的分泌。
Proc Natl Acad Sci U S A. 1986 Dec;83(24):9338-42. doi: 10.1073/pnas.83.24.9338.
5
Intracellular assembly and packaging of hepatitis B surface antigen particles occur in the endoplasmic reticulum.乙型肝炎表面抗原颗粒的细胞内组装和包装发生在内质网中。
J Virol. 1986 Jun;58(3):884-92. doi: 10.1128/JVI.58.3.884-892.1986.
6
A unique amino acid substitution, L215Q, in the hepatitis B virus small envelope protein of a genotype F isolate that inhibits secretion of hepatitis B virus subviral particles.基因型F分离株的乙型肝炎病毒小包膜蛋白中一种独特的氨基酸取代L215Q,可抑制乙型肝炎病毒亚病毒颗粒的分泌。
Intervirology. 2008;51(2):81-6. doi: 10.1159/000127430. Epub 2008 Apr 22.
7
Expression of hepatitis B virus large envelope polypeptide inhibits hepatitis B surface antigen secretion in transgenic mice.
J Virol. 1986 Dec;60(3):880-7. doi: 10.1128/JVI.60.3.880-887.1986.
8
Mutual dependence of Na,K-ATPase alpha- and beta-subunits for correct posttranslational processing and intracellular transport.钠钾ATP酶α亚基和β亚基在正确的翻译后加工及细胞内运输中的相互依赖性。
FEBS Lett. 1990 Aug 20;269(1):105-8. doi: 10.1016/0014-5793(90)81130-g.
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Presentation of the hydrophilic domains of hepatitis C viral E2 envelope glycoprotein on hepatitis B surface antigen particles.丙型肝炎病毒E2包膜糖蛋白亲水区在乙型肝炎表面抗原颗粒上的呈现
J Med Virol. 1996 Oct;50(2):145-51. doi: 10.1002/(SICI)1096-9071(199610)50:2<145::AID-JMV7>3.0.CO;2-A.
10
Mutational analysis of hepatitis B surface antigen particle assembly and secretion.乙型肝炎表面抗原颗粒组装与分泌的突变分析
J Virol. 1991 Jul;65(7):3813-20. doi: 10.1128/JVI.65.7.3813-3820.1991.

引用本文的文献

1
Secreted hepatitis B surface antigen polypeptides are derived from a transmembrane precursor.分泌型乙肝表面抗原多肽源自一种跨膜前体。
J Cell Biol. 1988 Dec;107(6 Pt 1):2163-8. doi: 10.1083/jcb.107.6.2163.
2
Expression and characterization of hepatitis B virus surface antigen polypeptides in insect cells with a baculovirus expression system.利用杆状病毒表达系统在昆虫细胞中表达和鉴定乙型肝炎病毒表面抗原多肽
J Virol. 1989 Apr;63(4):1549-57. doi: 10.1128/JVI.63.4.1549-1557.1989.