Figure 1.
Figure 1. A rhoptry-derived P falciparum parasite molecule binds to the surface of normal and infected erythrocytes. Staining of nEs and IEs from FCR3CSA parasites using mAb B4 (green) in IFA. Parasite DNA is stained with DAPI (blue). (A-D) L-IFA analysis. (E-H) AD-IFA analysis. (A) Merozoite binding to the membrane of an nE stained with anti–RSP-2. (B) Surface staining of an nE (left) and rIE (right). (C) Transfer of RSP-2 from merozoite to the entire erythrocyte surface. (D) A mature trophozoite-stage parasite is not stained by mAb B4. AD-IFA using B4 in young rIEs. (E) Endoplasmic reticulum (ER) in 26 ± 2–hour-old parasites. (F) Rhoptries in 34 ± 2–hour-old schizont stage (G) and surface of free merozoites at 44 ± 2 hours (H). Scale bars measure 10 μm.

A rhoptry-derived P falciparum parasite molecule binds to the surface of normal and infected erythrocytes. Staining of nEs and IEs from FCR3CSA parasites using mAb B4 (green) in IFA. Parasite DNA is stained with DAPI (blue). (A-D) L-IFA analysis. (E-H) AD-IFA analysis. (A) Merozoite binding to the membrane of an nE stained with anti–RSP-2. (B) Surface staining of an nE (left) and rIE (right). (C) Transfer of RSP-2 from merozoite to the entire erythrocyte surface. (D) A mature trophozoite-stage parasite is not stained by mAb B4. AD-IFA using B4 in young rIEs. (E) Endoplasmic reticulum (ER) in 26 ± 2–hour-old parasites. (F) Rhoptries in 34 ± 2–hour-old schizont stage (G) and surface of free merozoites at 44 ± 2 hours (H). Scale bars measure 10 μm.

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