Figure 2
Figure 2. Structure and trafficking to Maurer clefts. (A) Localization of the resident Maurer clefts markers PfSBP1 and PfMAHRP1 in parental CS2 (first row of each panel) and CS2ΔSBP1-infected cells (second row of each panel). PfMAHRP1 was correctly trafficked to Maurer clefts in both cell lines, whereas PfSBP1 showed only cross-reactivity with another protein within the parasite CS2ΔSBP1 without localization on Maurer clefts as observed in the parental CS2 cells. (B) Ultrastructural analysis of CS2- (top) and CS2ΔSBP1-infected cells (bottom) shows typical Maurer clefts in both cell lines. Bars represent 0.5 μm.

Structure and trafficking to Maurer clefts. (A) Localization of the resident Maurer clefts markers PfSBP1 and PfMAHRP1 in parental CS2 (first row of each panel) and CS2ΔSBP1-infected cells (second row of each panel). PfMAHRP1 was correctly trafficked to Maurer clefts in both cell lines, whereas PfSBP1 showed only cross-reactivity with another protein within the parasite CS2ΔSBP1 without localization on Maurer clefts as observed in the parental CS2 cells. (B) Ultrastructural analysis of CS2- (top) and CS2ΔSBP1-infected cells (bottom) shows typical Maurer clefts in both cell lines. Bars represent 0.5 μm.

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