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Merozoite surface protein 1 (MSP1) has been identified as a target antigen for protective immune responses against asexual blood stage malaria, but effective vaccines based on MSP1 have not been developed so far. We have modified the sequence of  Plasmodium yoelii  MSP1 19  (the C-terminal region of the molecule) and examined the ability of the variant proteins to bind protective monoclonal antibodies and to induce protection by immunization. In parallel, we examined the structure of the protein and the consequences of the amino acid changes. Naturally occurring sequence polymorphisms reduced the binding of individual protective antibodies, indicating that they contribute to immune evasion, but immunization with these variant proteins still provided protective immunity. One variant that resulted in the localized distortion of a loop close to the N-terminus of MSP1 19  almost completely ablated protection by immunization, indicating the importance of this region of MSP1 19  as a target for protective immunity and in vaccine development.

The structure ofPlasmodium yoeliimerozoite surface protein 119, antibody specificity and implications for malaria vaccine design

The structure ofPlasmodium yoeliimerozoite surface protein 1₁₉, antibody specificity and implications for malaria vaccine design