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Structural modifications to a high-activity binding peptide located within the PfEMP1 NTS domain induce protection against P. falciparum malaria in Aotus monkeysBinding activity, structure, and immunogenicity of synthetic peptides derived from Plasmodium falciparum CelTOS and TRSP proteinsPlasmodium falciparum rhoptry neck protein 5 peptides bind to human red blood cells and inhibit parasite invasionIdentifying putative Mycobacterium tuberculosis Rv2004c protein sequences that bind specifically to U937 macrophages and A549 epithelial cellsThe Mycobacterium tuberculosis membrane protein Rv2560--biochemical and functional studiesFunctional characterization of Mycobacterium tuberculosis Rv2969c membrane proteinCharacterising Mycobacterium tuberculosis Rv1510c protein and determining its sequences that specifically bind to two target cell linesMycobacterium tuberculosis Rv2536 protein implicated in specific binding to human cell linesIdentifying Plasmodium falciparum merozoite surface protein-10 human erythrocyte specific binding regionsPlasmodium falciparum normocyte binding protein (PfNBP-1) peptides bind specifically to human erythrocytes.P. falciparum: merozoite surface protein-8 peptides bind specifically to human erythrocytes.Fine mapping of Plasmodium falciparum ribosomal phosphoprotein PfP0 revealed sequences with highly specific binding activity to human red blood cells.Mycobacterium tuberculosis Rv0679c protein sequences involved in host-cell infection: potential TB vaccine candidate antigen.Specific interaction between Mycobacterium tuberculosis lipoprotein-derived peptides and target cells inhibits mycobacterial entry in vitro.Using the PfEMP1 head structure binding motif to deal a blow at severe malaria.The Plasmodium vivax rhoptry neck protein 5 is expressed in the apical pole of Plasmodium vivax VCG-1 strain schizonts and binds to human reticulocytes.Mammaglobin peptide as a novel biomarker for breast cancer detection.Identification of Plasmodium falciparum RhopH3 protein peptides that specifically bind to erythrocytes and inhibit merozoite invasion.Annotation and characterization of the Plasmodium vivax rhoptry neck protein 4 (PvRON4)Functional, immunological and three-dimensional analysis of chemically synthesised sporozoite peptides as components of a fully-effective antimalarial vaccine.Recent advances in the development of a chemically synthesised anti-malarial vaccine.Immune protection-inducing protein structures (IMPIPS) against malaria: the weapons needed for beating Odysseus.Mce4F Mycobacterium tuberculosis protein peptides can inhibit invasion of human cell lines.Peptides derived from Mycobacterium tuberculosis Rv2301 protein are involved in invasion to human epithelial cells and macrophages.Identification of peptides with high red blood cell and hepatocyte binding activity in the Plasmodium falciparum multi-stage invasion proteins: PfSPATR and MCP-1.Peptides derived from the Mycobacterium tuberculosis Rv1490 surface protein implicated in inhibition of epithelial cell entry: potential vaccine candidates?Characterizing the Mycobacterium tuberculosis Rv2707 protein and determining its sequences which specifically bind to two human cell lines.Liver stage antigen 3 Plasmodium falciparum peptides specifically interacting with HepG2 cells.Identifying Plasmodium falciparum merozoite surface antigen 3 (MSP3) protein peptides that bind specifically to erythrocytes and inhibit merozoite invasion.Characterization of Plasmodium falciparum integral membrane protein Pf25-IMP and identification of its red blood cell binding sequences inhibiting merozoite invasion in vitro.Identification of specific Hep G2 cell binding regions in Plasmodium falciparum sporozoite-threonine-asparagine-rich protein (STARP).Plasmodium falciparum: binding studies of peptide derived from the sporozoite surface protein 2 to Hep G2 cells.PvRON2, a new Plasmodium vivax rhoptry neck antigen.A Maurer's cleft-associated Plasmodium falciparum membrane-associated histidine-rich protein peptide specifically interacts with the erythrocyte membrane.Conserved regions from Plasmodium falciparum MSP11 specifically interact with host cells and have a potential role during merozoite invasion of red blood cells.Plasmodium vivax MSP-1 peptides have high specific binding activity to human reticulocytes.Synthetic peptides from conserved regions of the Plasmodium falciparum early transcribed membrane and ring exported proteins bind specifically to red blood cell proteins.Conserved regions of the Plasmodium falciparum rhoptry-associated protein 3 mediate specific host-pathogen interactions during invasion of red blood cells.Plasmodium falciparum EBA-140 kDa protein peptides that bind to human red blood cells.Protecting capacity against malaria of chemically defined tetramer forms based on the Plasmodium falciparum apical sushi protein as potential vaccine components.
P50
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P21
P31
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0000-0002-6556-7812