Department of Pathology, Georgetown University Medical School, 3900 Reservoir Rd. NW, Washington, DC 20057, USA.
J Virol. 2010 Feb;84(4):1696-703. doi: 10.1128/JVI.01968-09. Epub 2009 Dec 2.
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.
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。