Subcellular localization and quantitation of the human papillomavirus type 16 E6 oncoprotein through immunocytochemistry detection

被引:19
|
作者
Jackson, Robert [1 ,2 ]
Togtema, Melissa [1 ,2 ]
Zehbe, Ingeborg [1 ,2 ]
机构
[1] Probe Dev & Biomarker Explorat, Thunder Bay Reg Res Inst, 980 Oliver Rd, Thunder Bay, ON P7B 6V4, Canada
[2] Lakehead Univ, Dept Biol, Thunder Bay, ON P7B 5E1, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Human papillomavirus type 16 (HPV16); E6; oncoprotein; 4C6; antibody; SiHa; CaSki; Immunocytochemistry; Subcellular localization; Protein expression; MONOCLONAL-ANTIBODIES; CARCINOMA; EXPRESSION; PROTEIN; IDENTIFICATION; DEGRADATION; SEQUENCES; BINDING; DOMAIN; CELLS;
D O I
10.1016/j.virol.2012.09.032
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Human papillomavirus (HPV) type 16 E6 is a viral oncoprotein essential for host cell transformation. Due to its role in HPV-induced cancers of the genital, head and neck epithelia, reliable protein-level determination of E6 expression would be an invaluable diagnostic tool. Immunocytochemical detection and subcellular localization of HPV16 E6 has been demonstrated with varying success and a comprehensive review of techniques is lacking. To address these issues, we used established monoclonal antibodies and optimized a standard immunocytochemical method for E6 protein detection inside the HPV16 positive cell lines, SiHa and CaSki. E6 oncoprotein was detected primarily in the nucleus. We also refined quantitative analysis with a software to objectively differentiate between HPV16 positive and negative cells. Our analysis was also able to differentiate expression differences between SiHa and CaSki on par with RT-qPCR. Thus, we provide a long-needed, robust protocol for antibody-mediated detection of the HPV16 E6 oncoprotein inside cultured cells. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:425 / 432
页数:8
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