| 2007 |
In P. yoelii, deletion of P36 (together with P52) causes sporozoites to fail to form a parasitophorous vacuole (PV) within hepatocytes in vitro and in vivo; p52/p36-deficient parasites localized as free entities in host cell cytoplasm or nucleoplasm and did not develop as liver stages, establishing that P36 is essential for PV formation during hepatocyte invasion. |
Double-gene knockout by single genetic manipulation; immunofluorescence analysis; electron microscopy; in vitro and in vivo liver-stage growth assays |
Infection and immunity |
High |
17517871
|
| 2009 |
In P. falciparum, individual or simultaneous deletion of P36 (and P52) does not affect erythrocytic replication, gametocyte production, mosquito infection, or sporozoite production, but causes parasite developmental arrest during hepatocyte infection; the double-gene deletion exhibits a more severe intrahepatocytic growth defect than either single deletion. |
Double-crossover recombination gene deletion; in vitro liver-stage growth assay; chimeric mouse model with human hepatocytes |
Proceedings of the National Academy of Sciences of the United States of America |
High |
19625622
|
| 2015 |
In P. yoelii/P. falciparum sporozoites, P36 engages the host hepatocyte EphA2 receptor to establish the permissive parasitophorous vacuole; deletion of P36 phenocopies loss of host EphA2, and sporozoites productively infect hepatocytes with high EphA2 expression. |
Genetic deletion of P36 and EphA2; hepatocyte infection assays; EphA2 expression correlation with infectivity; mouse liver infection with EphA2 knockout |
Science (New York, N.Y.) |
Medium |
26612952
|
| 2017 |
P36 is a major parasite determinant of host cell receptor usage during sporozoite invasion of hepatocytes: P. falciparum P36 directs use of CD81, P. vivax P36 directs use of SR-BI, while P. berghei P36 is compatible with both receptors redundantly. Genetic analysis of sporozoite factors (swapping/deleting P36 across species) established this functional link between P36 and specific host cell receptors. |
Genetic analysis of sporozoite P36; hepatocyte infection assays with CD81- and SR-BI-deficient cells; cross-species comparison |
eLife |
High |
28506360
|
| 2018 |
In P. yoelii sporozoites, P36 localizes to micronemal secretory organelles and partially co-localizes with P52. P36 and P52 form a protein complex in sporozoites (demonstrated by co-immunoprecipitation). Upon sporozoite stimulation, P36 is released as a secreted protein whereas P52 is not, supporting a model in which GPI-anchored P52 scaffolds P36 for interaction with the host cell. Single deletion of P36 alone (as well as single deletion of P52 alone) causes loss of the PV after hepatocyte invasion, phenocopying the double deletion. |
Live imaging of P36-mCherry tagged parasite line; co-immunoprecipitation in vivo; immunofluorescence; single-gene knockout phenotype analysis |
Frontiers in cellular and infection microbiology |
High |
30547015
|
| 2012 |
The s48/45 domain structure (solved by NMR for the related Pf12 C-terminal domain) forms a β-sandwich with two sheets, conserved disulfide bonds linking the sheets, and structural homology to the SRS/SAG fold of Toxoplasma and to ephrins (ligands of Eph receptors), consistent with an adhesion function for P36 and other 6-cys family members. |
NMR structure determination of the Pf12 s48/45 domain; structural comparison |
Proceedings of the National Academy of Sciences of the United States of America |
Medium |
22493233
|
| 2012 |
In P. berghei, Δp52&p36 parasites that do develop in Huh-7 hepatocytes (a minor fraction) do so in the absence of an apparent parasitophorous vacuole membrane, either in the cytosol or nucleus; cytosolic Δp52&p36 parasites can fully mature and produce infectious merozoites, whereas nuclear ones cannot. |
Immunofluorescence; electron microscopy; in vitro hepatocyte culture (Huh-7); mouse blood-stage infection assay |
PloS one |
Medium |
23227206
|
| 2023 |
The B9 protein (another 6-cys family member) interacts with P36 and P52 in a heterologous expression system, suggesting P36 is part of a multi-protein invasion complex at the sporozoite surface. |
Heterologous expression system protein interaction assay (pulldown/co-expression) |
iScience |
Low |
36761022
|
| 2026 |
AlphaFold-based structural modeling combined with electron microscopy and small-angle X-ray scattering shows that P36 and P52 form a head-to-tail heterodimer with a conserved interaction interface across Plasmodium species. Epitope-tagged P36 variants combined with neutralization assays in P. berghei demonstrated that antibodies against epitopes on the membrane-distal side of the P36–P52 heterodimer efficiently block sporozoite invasion of hepatocytes in vitro, identifying vulnerable surface-exposed sites on P36 for antibody-mediated neutralization. |
AlphaFold structural modeling; electron microscopy; small-angle X-ray scattering; epitope-tagging of P36/P52; in vitro sporozoite neutralization assay in P. berghei |
PLoS pathogens |
High |
42418521
|