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Bifunctional Immunity Proteins Protect Bacteria against FtsZ-Targeting ADP-Ribosylating Toxins.
Ting, See-Yeun; Bosch, Dustin E; Mangiameli, Sarah M; Radey, Matthew C; Huang, Shuo; Park, Young-Jun; Kelly, Katherine A; Filip, Szymon Krzysztof; Goo, Young Ah; Eng, Jimmy K; Allaire, Marc; Veesler, David; Wiggins, Paul A; Peterson, S Brook; Mougous, Joseph D.
Afiliação
  • Ting SY; Department of Microbiology, University of Washington School of Medicine, Seattle, WA 98195, USA.
  • Bosch DE; Department of Pathology, University of Washington School of Medicine, Seattle, WA 98195, USA.
  • Mangiameli SM; Department of Physics, University of Washington, Seattle, WA 98195, USA.
  • Radey MC; Department of Microbiology, University of Washington School of Medicine, Seattle, WA 98195, USA.
  • Huang S; Department of Microbiology, University of Washington School of Medicine, Seattle, WA 98195, USA.
  • Park YJ; Department of Biochemistry, University of Washington School of Medicine, Seattle, WA 98195, USA.
  • Kelly KA; Department of Microbiology, University of Washington School of Medicine, Seattle, WA 98195, USA.
  • Filip SK; Proteomics Center of Excellence, Northwestern University, Chicago, IL 60611, USA.
  • Goo YA; Proteomics Center of Excellence, Northwestern University, Chicago, IL 60611, USA.
  • Eng JK; Proteomics Resource, University of Washington, Seattle, WA 98195, USA.
  • Allaire M; Molecular Biophysics and Integrated Bioimaging, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA.
  • Veesler D; Department of Biochemistry, University of Washington School of Medicine, Seattle, WA 98195, USA.
  • Wiggins PA; Department of Microbiology, University of Washington School of Medicine, Seattle, WA 98195, USA; Department of Physics, University of Washington, Seattle, WA 98195, USA; Department of Bioengineering, University of Washington, Seattle, WA 98195, USA.
  • Peterson SB; Department of Microbiology, University of Washington School of Medicine, Seattle, WA 98195, USA.
  • Mougous JD; Department of Microbiology, University of Washington School of Medicine, Seattle, WA 98195, USA; Department of Biochemistry, University of Washington School of Medicine, Seattle, WA 98195, USA; Howard Hughes Medical Institute, University of Washington, Seattle, WA 98195, USA. Electronic address: mou
Cell ; 175(5): 1380-1392.e14, 2018 11 15.
Article em En | MEDLINE | ID: mdl-30343895
ABSTRACT
ADP-ribosylation of proteins can profoundly impact their function and serves as an effective mechanism by which bacterial toxins impair eukaryotic cell processes. Here, we report the discovery that bacteria also employ ADP-ribosylating toxins against each other during interspecies competition. We demonstrate that one such toxin from Serratia proteamaculans interrupts the division of competing cells by modifying the essential bacterial tubulin-like protein, FtsZ, adjacent to its protomer interface, blocking its capacity to polymerize. The structure of the toxin in complex with its immunity determinant revealed two distinct modes of inhibition active site occlusion and enzymatic removal of ADP-ribose modifications. We show that each is sufficient to support toxin immunity; however, the latter additionally provides unprecedented broad protection against non-cognate ADP-ribosylating effectors. Our findings reveal how an interbacterial arms race has produced a unique solution for safeguarding the integrity of bacterial cell division machinery against inactivating post-translational modifications.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas de Bactérias / Toxinas Bacterianas / ADP Ribose Transferases / Proteínas do Citoesqueleto / N-Glicosil Hidrolases Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas de Bactérias / Toxinas Bacterianas / ADP Ribose Transferases / Proteínas do Citoesqueleto / N-Glicosil Hidrolases Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article