Proteins without TM that are located in the PV. a young and an old schizont are shown to illustrate the fact that some cells showed gaps in the fluorescence around the parasite (third row of images). The top microscopy panel row shows a ring and a trophozoite stage, the middle row shows a schizont and the bottom row shows a late schizont.Khosh-Naucke M, Becker J, Mesén-Ramírez P, Kiani P, Birnbaum J, Fröhlke U, Jonscher E, Schlüter H, Spielmann T. Identification of novel parasitophorous vacuole proteins in P. falciparum parasites using BioID. Int J Med Microbiol. 2017 Jul 27. [Epub ahead of print]

Saponin lysis during microscopy of a cell expressing parasitophorous vacuolar protein 2 (upper panel). The identical infected RBC is shown before (top row) and after (bottom row) lysis with saponin. release of the PV content using saponin did not abolish the signal in the parasite periphery, clearly showing that the signal around the parasite with PV2derives from the full-length protein. (B) A late schizont expressing serine/threonine protein phosphatase UIS2 (bottom panel) shows release of merozoites (arrow head) while the fluorescence still surrounds the bulk of the remainder of merozoites (top row) and no fluorescence is observed in released merozoites (bottom row). Some late stages were observed where merozoites had already been partially released but, in contrast to the merozoites in the remainder of the schizont, were not surrounded by GFP signal (arrowheads). As the released merozoites aresurrounded by PPM, this indicates that these proteins were associatedwith the PVM. In agreement with this, no fluorescence was observedwith fully released merozoites.Khosh-Naucke M, Becker J, Mesén-Ramírez P, Kiani P, Birnbaum J, Fröhlke U, Jonscher E, Schlüter H, Spielmann T. Identification of novel parasitophorous vacuole proteins in P. falciparum parasites using BioID. Int J Med Microbiol. 2017 Jul 27. [Epub ahead of print]