Two approximately 300 kilodalton Plasmodium falciparum proteins at the surface membrane of infected erythrocytes

• Published in: Molecular and biochemical parasitology Vol. 27; no. 2; pp. 207 - 223
• Main Authors: Howard, Russell J., Barnwell, John W., Rock, Edwin P., Neequaye, Janet, Ofori-Adjei, David, Lee Maloy, W., Lyon, Jeffrey A., Saul, Allan
• Format: Journal Article
• Language: English
• Published: Shannon Elsevier B.V 15.01.1988; Elsevier Science
• Subjects: Animals; Antibodies, Protozoan - immunology; Antigens, Protozoan - immunology; Antigens, Surface - immunology; Aotus trivirgatus - blood; Aotus trivirgatus - parasitology; Biochemistry. Physiology. Immunology. Molecular biology; Biological and medical sciences; Cytoadherence; Erythrocyte Membrane - immunology; Erythrocyte surface; Fundamental and applied biological sciences. Psychology; Human protozoal diseases; Humans; Infectious diseases; Malaria; Malarial antigen; Medical sciences; Molecular Weight; Monoclonal antibody; Parasitic diseases; Plasmodium falciparum; Plasmodium falciparum - analysis; Plasmodium falciparum - immunology; Protozoa; Protozoal diseases; Tropical medicine; MESA; SDS; Monoclonal antibody; P-RBC; Pf EMP; Erythrocyte surface; Plasmodium falciparum; SICA; McAb; K +B +, K +B −, K; Malarial antigen; Cytoadherence; Rα; Proteins; Protozoa; Intraerythrocytic cycle; Plasma membrane; Pathogen; Sporozoa; Molecular weight
• ISSN: 0166-6851; 1872-9428
• DOI: 10.1016/0166-6851(88)90040-0

Two very large Plasmodium falciparum proteins are identified as constituents of the infected erythrocyte membrane. Sera were obtained from Aotus monkeys that had been repeatedly infected with asexual P. falciparum from one of four strains. The capacity of these sera to block in vitro cytoadherence of infected erythrocytes and agglutinate intact infected cells was determined. The sera were also used to immunoprecipitate protein antigens from detergent extracts of 125I-surface labeled or biosynthetically radiolabeled infected erythrocytes. For each serum/antigen combination, precipitation of only one protein correlated with the ability of the serum to interfere with cytoadherence and agglutinate infected cells. This malarial protein, denoted Pf EMP 1 ( P. falciparum-erythrocyte-membrane-protein 1) bore strain-specific epitope(s) on the cell surface and displayed size heterogeneity ( M r ∼220 000–350 000). Pf EMP 1 was strongly labeled by cell-surface radioiodination but was a quantitatively very minor malarial protein. Pf EMP 1 was distinguished by its size, surface accessibility and antigenic properties from a more predominant malarial protein in the same size range (Pf EMP 2) that is under the infected erythrocyte membrane at knobs. Monoclonal antibodies and rabbit antisera raised against Pf EMP 2 were used to show that this size heterogeneous antigen was indistinguishable from the previously described MESA (mature parasite infected erythrocyte surface antigen), identified by precipitation with rabbit antisera raised against the MESA hexapeptide repeats. Antibodies raised against Pf EMP 2/MESA did not precipitate Pf EMP 1. We conclude that Pf EMP 1 is either directly responsible for the cytoadherence phenomenon, or is very closely associated with another as yet unidentified functional molecule. Pf EMP 2/MESA must have a structural property/function that is important under the host cell membrane.