Journal article

Structures of phage-display peptides that bind to the malarial surface protein, apical membrane antigen 1, and block erythrocyte invasion

DW Keizer, LA Miles, F Li, M Nair, RF Anders, AM Coley, M Foley, RS Norton

Biochemistry | Published : 2003

Abstract

Apical membrane antigen 1 (AMA1) of the human malaria parasite Plasmodiumfalciparum is synthesized by schizont stage parasites and has been implicated in merozoite invasion of host erythrocytes. Phage-display techniques have recently been used to identify two 15-residue peptides, F1 and F2, which bind specifically to P. falciparum AMA1 and inhibit parasite invasion of erythrocytes [Li, F., et al. (2002) J. Biol. Chem. 277, 50303-50310]. We have synthesized F1, F2, and three peptides with high levels of sequence identity, determined their relative binding affinities for P. falciparum AMA1 with a competition ELISA, and investigated their solution structures by NMR spectroscopy. The strongest b..

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University of Melbourne Researchers