Conserved high activity binding peptides from the Plasmodium falciparum Pf34 rhoptry protein inhibit merozoites in vitro invasion of red blood cells

Rhoptries are specialized secretory organelles found in all members of the genus Plasmodium whose proteins have been considered as promising vaccine candidates due to their involvement in cell invasion and the formation of the parasitophorous vacuole (PV). The Plasmodium falciparum Pf34 protein was recently identified as a rhoptry-neck protein located in detergent-resistant microdomains (DRMs) that is expressed in mature intraerythrocytic parasite stages, but its biological function is still unknown. Receptor-ligand assays carried out in this study found that peptides 36,051 ( 101DKKFSESLKAHMDHLKILNN120Y), 36,053 ( 141KKYIIKEIQNNKYLNKEKKS160), 36,055 ( 181WLESVNNIEEKSNILKNIKS200Y) and 36,056 ( 201QLLNNIASLNHTLSEEIKNI220Y), located in the central portion of Pf34, were found to establish protease-sensitive interactions of high affinity and specificity with receptors on the surface of red blood cell (RBCs). In vitro assays showed that Pf34 high activity binding peptides (HABPs) inhibit invasion of RBCs by P. falciparum merozoites, therefore suggesting that Pf34 could act as an adhesin during invasion and supporting the inclusion of Pf34 HABPs in further studies to develop antimalarial control methods. © 2010 Elsevier Inc. All rights reserved.

• Fecha de publicación: 2010
• Institución: Universidad del Rosario
• Repositorio: Repositorio EdocUR - U. Rosario
• Idioma: eng
• OAI Identifier: oai:repository.urosario.edu.co:10336/22785
• Acceso en línea: https://doi.org/10.1016/j.peptides.2010.07.009; https://repository.urosario.edu.co/handle/10336/22785
• Palabra clave: Adhesin; Antimalarial agent; High activity binding peptide 36051; High activity binding peptide 36053; High activity binding peptide 36055; High activity binding peptide 36056; Peptide derivative; Plasmodium falciparum pf34 protein; Protozoal protein; Unclassified drug; Amino acid sequence; Article; Cell invasion; Circular dichroism; Drug inhibition; Drug receptor binding; Erythrocyte; Human; Human cell; In vitro study; Merozoite; Plasmodium falciparum; Polymerase chain reaction; Priority journal; Protein interaction; Amino acid sequence; Animals; Erythrocytes; Humans; Membrane glycoproteins; Plasmodium falciparum; Protozoan proteins; Plasmodium falciparum; Detergent-resistant microdomains; Gpi-anchored; Peptides; Receptors; Vaccine
• License: Abierto (Texto Completo)