Species | Disruptability | Reference | Submitter |
---|---|---|---|
P. falciparum 3D7 |
Possible |
USF piggyBac screen (Insert. mut.) | USF PiggyBac Screen |
Location of native STEVOR at the iRBC surface. (A) Immunofluorescence assay of live 5A-infected erythrocytes with anti-S1 (upper row) and anti-S2 (middle row) antisera recognizing native STEVOR at the iRBC surface. Either anti-S1 or anti-S2 (lower row) did not react with trypsinized iRBC. The specific antibodies that reacted with the iRBC surface were detected with Alexa Fluor–labeled goat anti-rabbit IgG. Visualization of STEVOR surface antigens. Double staining of live 5A-iRBCs with either anti-S1 (or anti-S2) (panel i) with anti-Glycophorin C antibodies.Niang M, Yan Yam X, Preiser PR. The Plasmodium falciparum STEVOR Multigene Family Mediates Antigenic Variation of the Infected Erythrocyte. PLoS Pathog. 2009;5(2):e1000307. Epub 2009 Feb 20.
See original on MMPRepresentative images from fixed and live IFA of iRBCs from different clones. A4(tr-II) clone contains GFP tagged STEVOR. For fixed IFA, cells from 5A, A4 and A4 (tr-I ) clones were first treated with 4% paraformaldehyde for 15 minutes followed by permeabilization wtih 0.05% Triton X100. Permeabilized cells were then incubated with anti-S1 serum as the primary antibody. For 5A, the primary antibody was detected with PE conjugated goat anti-rabbit serum; for A4 and A4(tr-I), Alexa-488 conjugated donkey anti-rabbit serum was used as the secondary antibody. For live IFA, A4 and A4(tr-I) cells, after a 30 minutes incubation with 1% BSA, were directly incubated with anti-S1 serum followed by staining with Alexa-488 conjugated goat anti rabbit secondary antibody. A4(tr-II) cells were not incubated with any STEVOR antibody in live IFA assay. In each case, parasite was stained with 6-diaminido-2-phenylindole (DAPI, 2 mg/mL in PBS). Successive columns from left to right show the bright field, DAPI, STEVOR staining/GFP tag and merged images respectively. A4 clone does not exhibit any staining with anti-S1 serum in fixed and live IFA assays showing the lack of STEVOR proteins. Cells shown are representative of different asexual stages from cell population samples (White scale bar, 5μm; black scale bar, 5μm).Singh H, Madnani K, Lim YB, Cao J, Preiser PR, Lim CT. Expression dynamics and physiologically relevant functional study of STEVOR in asexual stages of Plasmodium falciparum infection. Cell Microbiol. 2017 Jun;19(6)
See original on MMPPlasmoDB | PF3D7_0617600 |
GeneDB | PF3D7_0617600 |
Malaria Metabolic Pathways | Localisation images Pathways mapped to |
Previous ID(s) | 2270.t00066, MAL6P1.251, PFF0850c |
Orthologs | |
Google Scholar | Search for all mentions of this gene |