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本文引用的文献

1
Characterization of the plasma membrane localization and orientation of HPV16 E5 for cell-cell fusion.人乳头瘤病毒16型E5蛋白在细胞间融合中的质膜定位及方向特征分析
Virology. 2009 Oct 10;393(1):135-43. doi: 10.1016/j.virol.2009.07.034. Epub 2009 Aug 26.
2
Papillomaviruses in the causation of human cancers - a brief historical account.人乳头瘤病毒在人类癌症病因中的作用——简要历史回顾
Virology. 2009 Feb 20;384(2):260-5. doi: 10.1016/j.virol.2008.11.046. Epub 2009 Jan 8.
3
Human papillomavirus 16 E5 induces bi-nucleated cell formation by cell-cell fusion.人乳头瘤病毒16 E5通过细胞-细胞融合诱导双核细胞形成。
Virology. 2009 Feb 5;384(1):125-34. doi: 10.1016/j.virol.2008.10.011. Epub 2008 Nov 28.
4
Epidemiology of human papillomavirus infection in men, cancers other than cervical and benign conditions.男性人乳头瘤病毒感染的流行病学、非宫颈癌及良性疾病
Vaccine. 2008 Aug 19;26 Suppl 10(0 10):K17-28. doi: 10.1016/j.vaccine.2008.06.021.
5
Host defenses against human papillomaviruses: lessons from epidermodysplasia verruciformis.宿主对人乳头瘤病毒的防御:来自疣状表皮发育不良的经验教训。
Curr Top Microbiol Immunol. 2008;321:59-83. doi: 10.1007/978-3-540-75203-5_3.
6
Koilocytosis: a cooperative interaction between the human papillomavirus E5 and E6 oncoproteins.凹空细胞形成:人乳头瘤病毒E5和E6癌蛋白之间的协同相互作用。
Am J Pathol. 2008 Sep;173(3):682-8. doi: 10.2353/ajpath.2008.080280. Epub 2008 Aug 7.
7
Bap31 is a novel target of the human papillomavirus E5 protein.Bap31是人类乳头瘤病毒E5蛋白的一个新靶点。
J Virol. 2008 Oct;82(20):10042-51. doi: 10.1128/JVI.01240-08. Epub 2008 Aug 6.
8
Karyopherin beta3: a new cellular target for the HPV-16 E5 oncoprotein.核转运蛋白β3:人乳头瘤病毒16型E5癌蛋白的新细胞靶点。
Biochem Biophys Res Commun. 2008 Jul 11;371(4):684-8. doi: 10.1016/j.bbrc.2008.04.122. Epub 2008 May 1.
9
The first hydrophobic region of the HPV16 E5 protein determines protein cellular location and facilitates anchorage-independent growth.人乳头瘤病毒16型E5蛋白的首个疏水区域决定蛋白质的细胞定位并促进不依赖贴壁的生长。
Virol J. 2008 Feb 26;5:30. doi: 10.1186/1743-422X-5-30.
10
Regulation of cellular zinc balance as a potential mechanism of EVER-mediated protection against pathogenesis by cutaneous oncogenic human papillomaviruses.细胞锌平衡的调节作为EVER介导的针对皮肤致癌性人乳头瘤病毒发病机制的潜在保护机制。
J Exp Med. 2008 Jan 21;205(1):35-42. doi: 10.1084/jem.20071311. Epub 2007 Dec 24.

人乳头瘤病毒 16 型 E5 癌蛋白的膜定向。

Membrane orientation of the human papillomavirus type 16 E5 oncoprotein.

机构信息

Department of Pathology, Georgetown University Medical School, 3900 Reservoir Rd. NW, Washington, DC 20057, USA.

出版信息

J Virol. 2010 Feb;84(4):1696-703. doi: 10.1128/JVI.01968-09. Epub 2009 Dec 2.

DOI:10.1128/JVI.01968-09
PMID:19955310
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2812368/
Abstract

The E5 protein of human papillomavirus type 16 is a small, hydrophobic protein that localizes predominantly to membranes of the endoplasmic reticulum (ER). To define the orientation of E5 in these membranes, we employed a differential, detergent permeabilization technique that makes use of the ability of low concentrations of digitonin to selectively permeabilize the plasma membrane and saponin to permeabilize all cellular membranes. We then generated a biologically active E5 protein that was epitope tagged at both its N and C termini and determined the accessibility of these termini to antibodies in the presence and absence of detergents. In both COS cells and human ectocervical cells, the C terminus of E5 was exposed to the cytoplasm, whereas the N terminus was restricted to the lumen of the ER. Finally, the deletion of the E5 third transmembrane domain (and terminal hydrophilic amino acids) resulted in a protein with its C terminus in the ER lumen. Taken together, these topology findings are compatible with a model of E5 being a 3-pass transmembrane protein and with studies demonstrating its C terminus interacting with cytoplasmic proteins.

摘要

人乳头瘤病毒 16 型的 E5 蛋白是一种小的疏水性蛋白,主要定位于内质网(ER)的膜上。为了确定 E5 在这些膜中的取向,我们采用了一种差速、去污剂渗透技术,该技术利用低浓度的脱氧胆酸钠选择性渗透质膜和皂素渗透所有细胞膜的能力。然后,我们生成了一种生物活性的 E5 蛋白,该蛋白在其 N 和 C 末端都被表位标记,并确定了在存在和不存在去污剂的情况下这些末端对抗体的可及性。在 COS 细胞和人宫颈外细胞中,E5 的 C 末端暴露于细胞质中,而 N 末端则局限于 ER 的腔中。最后,E5 的第三个跨膜结构域(和末端亲水氨基酸)的缺失导致其 C 末端位于 ER 腔中。总之,这些拓扑结构发现与 E5 是一种 3 次跨膜蛋白的模型以及证明其 C 末端与细胞质蛋白相互作用的研究结果一致。