Immunogenicity changes in melittin conjugates by structural modifications

V. Curcio-Vonlanthen, Zhenjun Zhao, H. P. Rolli, C. H. Schneider

Research output: Contribution to conferencePaper

Abstract

Peptides derived from the bee-venom melittin were fitted with the haptenic group dinitrocarboxyphenyl (Dncp) and tested in out-bred guinea pigs for immunogenicity by measuring the IgG anti-Dncp antibody response by ELISA. Dncp-conjugates comprising virtually the entire melittin proved to be strong immunogens producing antibody responses comparable to those of proteins. Weak responses were obtained with considerably shortened sequences. Conjugates with N-terminal Dncp gave markedly reduced antibody responses compared to peptides with C-terminal Dncp. An N-terminal biotinyl substituent abolished the immune response whereas N-terminal lauryl and caprylyl had little effect. Insertion of L-proline into a hexadecapeptide conjugate abolishing the possibility of helix formation gave an immunogen to which individual animals clearly responded on a low level. Oligomerisation, but not the cytolytic activity of melittin peptides, may contribute to the immunogenicities observed.
Original languageEnglish
Pages843-844
Number of pages2
Publication statusPublished - 1994
Externally publishedYes
Event23rd European peptide symposium - Braga, Portugal
Duration: 4 Sep 199410 Sep 1994

Conference

Conference23rd European peptide symposium
CountryPortugal
CityBraga
Period4/09/9410/09/94

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  • Cite this

    Curcio-Vonlanthen, V., Zhao, Z., Rolli, H. P., & Schneider, C. H. (1994). Immunogenicity changes in melittin conjugates by structural modifications. 843-844. Paper presented at 23rd European peptide symposium, Braga, Portugal.