Figure 3
Figure 3. KAHRP is trafficked normally to the erythrocyte membrane and assembled into knob structures. (A) Immunofluorescence assay to determine the localization of KAHRP in parental CS2 (top) and CS2ΔSBP1-infected erythrocytes (bottom). Cells were reacted with anti-KAHRP antibodies and identical localization patterns for both parasite lines were observed. (B) Scanning electron microscopy revealed typical knob structures in CS2ΔSBP1 parasite-infected erythrocytes compared with parental CS2. The panel shows a representative trophozoite-infected erythrocyte of each cell line. The bar represents 2 μm. (C) Ultrastructural analysis of CS2- and CS2ΔSBP1-infected cells of knob structures (arrow).

KAHRP is trafficked normally to the erythrocyte membrane and assembled into knob structures. (A) Immunofluorescence assay to determine the localization of KAHRP in parental CS2 (top) and CS2ΔSBP1-infected erythrocytes (bottom). Cells were reacted with anti-KAHRP antibodies and identical localization patterns for both parasite lines were observed. (B) Scanning electron microscopy revealed typical knob structures in CS2ΔSBP1 parasite-infected erythrocytes compared with parental CS2. The panel shows a representative trophozoite-infected erythrocyte of each cell line. The bar represents 2 μm. (C) Ultrastructural analysis of CS2- and CS2ΔSBP1-infected cells of knob structures (arrow).

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