1. Structural and functional insights into the delivery of a bacterial Rhs pore-forming toxin to the membrane
- Author
-
Wellcome Trust, Biotechnology and Biological Sciences Research Council (UK), Medical Research Council (UK), Fundación Biofísica Bizkaia, Ministerio de Ciencia e Innovación (España), European Commission, Agencia Estatal de Investigación (España), Eusko Jaurlaritza, Ikerbasque Basque Foundation for Science, Ministerio de Ciencia, Innovación y Universidades (España), Canadian HIV Trials Network Canadian Institutes of Health Research, Universidad Jaime I, Generalitat Valenciana, Burroughs Wellcome Fund, González-Magaña, Amaia [0000-0002-6007-8390], Tascón, Igor [0000-0003-2526-6238], Altuna, Jon [0000-0002-4993-7991], Albesa-Jové, David [0000-0003-2904-8203], González-Magaña, Amaia, Tascón, Igor, Altuna, Jon, Queralt, María, Colautti, Jake, Velázquez, Carmen, Zabala, Maialen, Rojas-Palomino, Jessica, Cárdenas, Marité, Alcaraz, Antonio, Whitney, John C., Ubarretxena, Iban, Albesa-Jové, David, Wellcome Trust, Biotechnology and Biological Sciences Research Council (UK), Medical Research Council (UK), Fundación Biofísica Bizkaia, Ministerio de Ciencia e Innovación (España), European Commission, Agencia Estatal de Investigación (España), Eusko Jaurlaritza, Ikerbasque Basque Foundation for Science, Ministerio de Ciencia, Innovación y Universidades (España), Canadian HIV Trials Network Canadian Institutes of Health Research, Universidad Jaime I, Generalitat Valenciana, Burroughs Wellcome Fund, González-Magaña, Amaia [0000-0002-6007-8390], Tascón, Igor [0000-0003-2526-6238], Altuna, Jon [0000-0002-4993-7991], Albesa-Jové, David [0000-0003-2904-8203], González-Magaña, Amaia, Tascón, Igor, Altuna, Jon, Queralt, María, Colautti, Jake, Velázquez, Carmen, Zabala, Maialen, Rojas-Palomino, Jessica, Cárdenas, Marité, Alcaraz, Antonio, Whitney, John C., Ubarretxena, Iban, and Albesa-Jové, David
- Abstract
Bacterial competition is a significant driver of toxin polymorphism, which allows continual compensatory evolution between toxins and the resistance developed to overcome their activity. Bacterial Rearrangement hot spot (Rhs) proteins represent a widespread example of toxin polymorphism. Here, we present the 2.45 Å cryo-electron microscopy structure of Tse5, an Rhs protein central to Pseudomonas aeruginosa type VI secretion system-mediated bacterial competition. This structural insight, coupled with an extensive array of biophysical and genetic investigations, unravels the multifaceted functional mechanisms of Tse5. The data suggest that interfacial Tse5-membrane binding delivers its encapsulated pore-forming toxin fragment to the target bacterial membrane, where it assembles pores that cause cell depolarisation and, ultimately, bacterial death.
- Published
- 2023