Epitope mapping of the human papillomavirus type 16 E4 protein by means of synthetic peptides

1 Department of Experimental Virology, Institute of Hematology and Blood Transfusion, Korunní 108, 101 03 Prague 10 and 2 Department of Synthetic Peptides, Institute of Sera and Vaccines, Prague, Czechoslovakia Eight overlapping icosapeptides covering the entire sequence of the E4 protein of human p...

Full description

Saved in:
Bibliographic Details
Published inJournal of general virology Vol. 73; no. 2; pp. 429 - 432
Main Authors Suchankova, A, Krchnak, V, Vagner, J, Hamsikova, E, Krcmar, M, Ritterova, L, Vonka, V
Format Journal Article
LanguageEnglish
Published Reading Soc General Microbiol 01.02.1992
Society for General Microbiology
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:1 Department of Experimental Virology, Institute of Hematology and Blood Transfusion, Korunní 108, 101 03 Prague 10 and 2 Department of Synthetic Peptides, Institute of Sera and Vaccines, Prague, Czechoslovakia Eight overlapping icosapeptides covering the entire sequence of the E4 protein of human papillomavirus type 16 (HPV-16), were prepared and tested for their reactivity with human sera in IgG-specific ELISA. The strongest reactivity of sera from HPV-16 DNA-positive invasive cervical carcinoma (INCA) patients was detected with the peptide denoted 16/E4-6, covering amino acids 51 to 70. Subsequently nearly 200 sera were tested for the presence of the 16/E4-6-specific antibody. Reactivity was more frequent in cervical intraepithelial neoplasia patients and INCA patients than in matched control subjects. Sera from INCA patients were also tested for antibody reactive with peptide 16/E7-2 covering the major type-specific reactive region of the HPV-16 E7 protein. Only four of 13 sera possessing the 16/E4-6-specific antibody were reactive with the 16/E7-2 peptide. Received 23 July 1991; accepted 31 October 1991.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ObjectType-Article-1
ObjectType-Feature-2
ISSN:0022-1317
1465-2099
DOI:10.1099/0022-1317-73-2-429