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J Gen Virol 70 (1989), 2973-2987; DOI 10.1099/0022-1317-70-11-2973
© 1989 Society for General Microbiology

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Identification of Immunogenic Regions of the Major Coat Protein of Human Papillomavirus Type 16 that Contain Type-restricted Epitopes

John Cason1, Daksha Patel2,{dagger}, Jennifer Naylor2, Declan Lunney2, Philip S. Shepherd3, Jennifer M. Best1 and Dennis J. McCance1

The1 Richard Dimbleby Laboratory of Cancer Virology, St Thomas' Campus, Lambeth Palace Road, London SE1 7EH
and2 Department of Microbiology
and3 Department of Immunology, United Medical and Dental Schools of Guy's and St Thomas' Hospitals, Guy's Campus, London Bridge, London SE1 9RT, U.K.

We have identified regions of the major capsid protein, L1, of the human papillomavirus (HPV) type 16 (HPV-16 L1), that are recognized by five monoclonal antibodies (MAbs) raised to a bacterial fusion protein containing residues 172 to 375 of HPV-16 L1. All five MAbs recognized HPV-16-infected tissue sections by immuno-histochemistry, but not sections infected with HPV-1a (cutaneous warts), HPV-6b or -11 (genital warts). MAbs 3D1, 5A4 and 1D6 also recognized HPV-2-infected sections (cutaneous warts); MAb 8C4 recognized only sections containing HPV-16. Four MAbs (8C4, 3D1, 1D6 and 5A4) recognized a synthetic peptide corresponding to residues 269 to 284 of HPV-16 L1; within this region a minimum antibody binding site was identified, a tripeptide 276 to 278. However the complete epitope appears to extend beyond these residues and beyond HPV-16 L1 (269 to 284). The fifth MAb, 1C6, recognized bacterial fusion proteins containing HPV-6b L1, -16 L1 or -18 L1 using immunoblots, yet appeared HPV-16-specific when tested on infected tissue sections. This MAb recognized five amino acids within a different region of HPV-16 L1 (residues 299 to 313).

Keywords: HPV-16, L1 coat protein, monoclonal antibodies

{dagger} Present address: Howard Hughes Medical Institute, Department of Molecular Genetics and Cell Biology, University of Chicago, Chicago, Illinois 60617, U.S.A.

Received 10 April 1989; accepted 7 July 1989.


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