A Novel Phosphatidylinositol 4,5-Bisphosphate Binding Domain Mediates Plasma Membrane Localization of ExoU and Other Patatin-like Phospholipases
| Autor: | Hyunjin Kim, Karla J. Satchell, Brett Geissler, Andrei S. Halavaty, Mallory J. Agard, Alan R. Hauser, Gregory H. Tyson, Wayne F. Anderson, Wonhwa Cho |
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| Rok vydání: | 2015 |
| Předmět: |
Phosphatidylinositol 4
5-Diphosphate Plasma protein binding Pseudomonas fluorescens Microbiology Biochemistry Protein Structure Secondary Type three secretion system Cell membrane chemistry.chemical_compound fluids and secretions Phospholipase A2 Bacterial Proteins medicine Humans Phosphatidylinositol Molecular Biology biology Effector Cell Membrane Cell Biology bacterial infections and mycoses digestive system diseases Cell biology medicine.anatomical_structure Phosphatidylinositol 4 5-bisphosphate chemistry Phospholipases Pseudomonas aeruginosa biology.protein bacteria Photorhabdus HeLa Cells Protein Binding Binding domain |
| Zdroj: | Journal of Biological Chemistry. 290:2919-2937 |
| ISSN: | 0021-9258 |
| DOI: | 10.1074/jbc.m114.611251 |
| Popis: | Bacterial toxins require localization to specific intracellular compartments following injection into host cells. In this study, we examined the membrane targeting of a broad family of bacterial proteins, the patatin-like phospholipases. The best characterized member of this family is ExoU, an effector of the Pseudomonas aeruginosa type III secretion system. Upon injection into host cells, ExoU localizes to the plasma membrane, where it uses its phospholipase A2 activity to lyse infected cells. The targeting mechanism of ExoU is poorly characterized, but it was recently found to bind to the phospholipid phosphatidylinositol 4,5-bisphosphate (PI(4,5)P2), a marker for the plasma membrane of eukaryotic cells. We confirmed that the membrane localization domain (MLD) of ExoU had a direct affinity for PI(4,5)P2, and we determined that this binding was required for ExoU localization. Previously uncharacterized ExoU homologs from Pseudomonas fluorescens and Photorhabdus asymbiotica also localized to the plasma membrane and required PI(4,5)P2 for this localization. A conserved arginine within the MLD was critical for interaction of each protein with PI(4,5)P2 and for localization. Furthermore, we determined the crystal structure of the full-length P. fluorescens ExoU and found that it was similar to that of P. aeruginosa ExoU. Each MLD contains a four-helical bundle, with the conserved arginine exposed at its cap to allow for interaction with the negatively charged PI(4,5)P2. Overall, these findings provide a structural explanation for the targeting of patatin-like phospholipases to the plasma membrane and define the MLD of ExoU as a member of a new class of PI(4,5)P2 binding domains. |
| Databáze: | OpenAIRE |
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