A Comprehensive Subcellular Atlas of the Toxoplasma Proteome via hyperLOPIT Provides Spatial Context for Protein Functions.
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IF: 31.316
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Cited by: 158
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Abstract

Apicomplexan parasites cause major human disease and food insecurity. They owe their considerable success to highly specialized cell compartments and structures. These adaptations drive their recognition, nondestructive penetration, and elaborate reengineering of the host's cells to promote their growth, dissemination, and the countering of host defenses. The evolution of unique apicomplexan cellular compartments is concomitant with vast proteomic novelty. Consequently, half of apicomplexan proteins are unique and uncharacterized. Here, we determine the steady-state subcellular location of thousands of proteins simultaneously within the globally prevalent apicomplexan parasite Toxoplasma gondii. This provides unprecedented comprehensive molecular definition of these unicellular eukaryotes and their specialized compartments, and these data reveal the spatial organizations of protein expression and function, adaptation to hosts, and the underlying evolutionary trajectories of these pathogens.

Keywords

Spatial Omics
IMC
Spatial Gene Expression
apicomplexa
evolution
host-pathogen interaction
invasion
organelle
parasitism
plasmodium
proteomics
subcellular
toxoplasma

MeSH terms

Apicomplexa
Biological Evolution
Epitopes
Host-Pathogen Interactions
Humans
Proteome
Proteomics
Protozoan Proteins
Toxoplasma

Authors

Barylyuk, Konstantin
Koreny, Ludek
Ke, Huiling
Butterworth, Simon
Crook, Oliver M
Lassadi, Imen
Gupta, Vipul
Tromer, Eelco
Mourier, Tobias
Stevens, Tim J
Breckels, Lisa M
Pain, Arnab
Lilley, Kathryn S
Waller, Ross F

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