Improved immunodetection of human papillomavirus E7.
- Author:
Ju Hong JEON
1
;
Sung Yup CHO
;
Chai Wan KIM
;
Dong Myung SHIN
;
Joon Cheol KWON
;
Kyung Ho CHOI
;
In Gyu KIM
Author Information
1. Department of Biochemistry and Molecular Biology, Aging Apoptosis Research Center (AARC), Seoul National University College of Medicine, Seoul, Korea. igkim@plaza.snu.ac.kr
- Publication Type:Original Article ; Research Support, Non-U.S. Gov't
- Keywords:
glutaral;
immunoblotting;
immunologic techniques;
oncogene proteins;
viral;
papillomavirus;
human
- MeSH:
Cell Extracts/chemistry/immunology;
Cell Line;
Human;
Immunochemistry/*methods;
Oncogene Proteins, Viral/*analysis/immunology;
Papillomavirus, Human/chemistry/*immunology
- From:Experimental & Molecular Medicine
2002;34(6):496-499
- CountryRepublic of Korea
- Language:English
-
Abstract:
Human papillomavirus E7 (HPV E7) is a viral oncoprotein that plays an important role in cervical carcinogenesis through binding with retinoblastoma protein (Rb). Inactivation of Rb by E7 is necessary but not sufficient for cellular transformation, suggesting other protein-protein interactions are required for E7-mediated cellular transformation aside from the interaction with Rb. However, studies on the oncogenic function of HPV E7 have been limited by its poor immunoreactivity. In this report, we show that the fixation of purified recombinant HPV E7 on blotted nitrocellulose membrane with glutaldehyde markedly enhanced the immunoreactivity of HPV E7 protein. Using HeLa and Caski cell line which are infected with HPV 18 and HPV 16, respectively, we demonstrated that native HPV E7 proteins also could be detected by this method. These results therefore can provide the experimental conditions for detection of HPV E7 proteins with greater sensitivity and may help to analyze E7 functions.
