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Programmer (design), Fremont, CA. Epitopes from six different strains of Plasmodium falciparum were fused to the PfSEA3D protein and expressed as recombinant antigen by a keyhole limpet haemocyanin signal. The 6-mer, 25-mer, and octapeptide antigens derived from the fcr4/33 genome sequence were tested in ELISAs with two sets of sera (simian and human). Results show that the 25-mer is the best candidate for incorporating in an antimalarial vaccine. Besides SEA, PfSEARPs and PfSEA3D were also investigated for vaccine development. Overall, the PfSEARPs domain does not contribute significantly to the protective effect of PfSEA3D. In addition, the PfSEA3D protein without a transmembrane segment as well as the C-terminal portion of PfSEA3D are capable of eliciting good antisera responses when fused to the MUC1 cancer antigens. A unique dimer association that may stabilize PfSEA3D is shown by NMR experiments. Our antisera results show that the conserved structure of this domain that is known to undergo very little variation may be important for antimalarial antibody responses.
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[Extra speed] sam broadcaster 4.9.2 crack added 1
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