A Plasmodium falciparum antigen containing clusters of asparagine residues.
Author(s) -
Marie Wahlgren,
Lena Åslund,
Lovisa Franzén,
Mats Sundvall,
B Wåhlin,
Kathryn Berzins,
Lore' Anne McNicol,
Anders Björkman,
Hans Wigzell,
Peter Perlmann
Publication year - 1986
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.83.8.2677
Subject(s) - polyclonal antibodies , antigen , antiserum , plasmodium falciparum , microbiology and biotechnology , epitope , merozoite surface protein , monoclonal antibody , asparagine , biology , antibody , immunofluorescence , virology , chemistry , biochemistry , malaria vaccine , amino acid , malaria , immunology
A genomic DNA fragment that encodes a Plasmodium falciparum antigen has been isolated by using human antibodies eluted from the membrane of infected erythrocytes. The antigen has a very unusual primary structure; it is exceptionally rich in asparagine residues, many of which are distributed in clusters (2-15 residues) along the polypeptide chain. Unlike many P. falciparum antigens, this protein lacks tandemly repeated sequences. The antigen is distinct from Pf 155, a merozoite-derived antigen deposited in the membrane of infected erythrocytes, but contains epitopes that crossreact with anti-Pf 155 antibodies. Antisera prepared in mice against the asparagine-rich protein react with late-stage parasites in indirect immunofluorescence. In an in vitro merozoite reinvasion assay, the IgG fraction of a mouse polyclonal antiserum, as well as a mouse monoclonal antibody, gave significant inhibition. Three polypeptides (Mr 36,000, 30,000, and 15,000) were recognized by these antibodies on immunoblots of P. falciparum extracts.
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