A novel platform for peptide-mediated affinity capture and LC-MS/MS identification of host receptors involved in Plasmodium invasion

Keyphrases

• Plasmodium 100%
• Red Blood Cells 100%
• Host Receptor 100%
• Affinity Capture 100%
• LC-MS Characterization 100%
• Synthetic Peptides 42%
• Plasmodium Falciparum 42%
• Ghosts 42%
• Parasite Proteins 28%
• Red Blood Cell Membrane 28%
• Basigin 28%
• Liquid Chromatography-tandem Mass Spectrometry (LC-MS/MS) 28%
• PfRH5 28%
• Parasite Biology 28%
• Sigma-1 Receptor 28%
• Malaria 14%
• Therapeutic Potential 14%
• Disease Pathogenesis 14%
• Derived Peptide 14%
• Cell Membrane Proteins 14%
• Cell Wall Proteins 14%
• Erythrocytes 14%
• Malarial Parasite 14%
• Protein Extract 14%
• Binding Ability 14%
• Binding Capacity 14%
• Cell Surface Receptor 14%
• Peptide Affinity 14%
• Molecular Interactions 14%
• Putative Drug Targets 14%
• LC-MS Analysis 14%
• Debilitating Disease 14%
• Capture Assay 14%
• Specific Receptor 14%
• Receptor-based 14%
• Cell Binding 14%
• Reticulocyte-binding Protein Homolog 5 14%

Immunology and Microbiology

• Plasmodium 100%
• Peptides 100%
• Tandem Mass Spectrometry 100%
• Liquid Chromatography Mass Spectrometry 100%
• Erythrocyte 100%
• Plasmodium falciparum 50%
• Erythrocyte Ghost 50%
• Parasite Protein 33%
• Erythrocyte Membrane 33%
• Basigin 33%
• Parasite Biology 33%
• Protein Binding 16%
• Reticulocyte 16%
• Molecular Interaction 16%
• Malaria 16%
• Therapeutic Target 16%

Biochemistry, Genetics and Molecular Biology

• Plasmodium 100%
• Liquid Chromatography-Mass Spectrometry 100%
• Peptide 100%
• Tandem Mass Spectrometry 100%
• Parasite 80%
• Plasmodium falciparum 60%
• Erythrocyte Ghost 60%
• Erythrocyte Membrane 40%
• Hemocyte 40%
• Basigin 40%
• Binding Protein 20%
• Reticulocyte 20%
• Membrane Protein 20%
• Molecular Interaction 20%