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Serum-Mediated Cleavage of Bacillus anthracis Protective Antigen Is a Two-Step Process That Involves a Serum Carboxypeptidase.
Goldman, David L; Nieves, Edward; Nakouzi, Antonio; Rivera, Johanna; Phyu, Ei Ei; Win, Than Htut; Achkar, Jacqueline M; Casadevall, Arturo.
Afiliación
  • Goldman DL; Department of Microbiology and Immunology, Einstein College of Medicine, Bronx, New York, USA david.goldman@einstein.yu.edu.
  • Nieves E; Department of Pediatrics, Einstein College of Medicine, Bronx, New York, USA.
  • Nakouzi A; The Children's Hospital at Montefiore, Bronx, New York, USA.
  • Rivera J; Department of Biochemistry, Einstein College of Medicine, Bronx, New York, USA.
  • Phyu EE; Department of Microbiology and Immunology, Einstein College of Medicine, Bronx, New York, USA.
  • Win TH; Department of Microbiology and Immunology, Einstein College of Medicine, Bronx, New York, USA.
  • Achkar JM; Department of Pediatrics, Einstein College of Medicine, Bronx, New York, USA.
  • Casadevall A; Department of Pediatrics, Einstein College of Medicine, Bronx, New York, USA.
mSphere ; 3(3)2018 06 27.
Article en En | MEDLINE | ID: mdl-29950379
Much of our understanding of the activity of anthrax toxin is based on in vitro systems, which delineate the interaction between Bacillus anthracis toxins and the cell surface. However, these systems fail to account for the intimate association of B. anthracis with the circulatory system, including the contribution of serum proteins to the host response and processing of anthrax toxins. Using a variety of immunological techniques to inhibit serum processing of B. anthracis protective antigen (PA) along with mass spectrometry analysis, we demonstrate that serum digests PA via 2 distinct reactions. In the first reaction, serum cleaves PA83 into 2 fragments to produce PA63 and PA20 fragments, similarly to that observed following furin digestion. This is followed by carboxypeptidase-mediated removal of the carboxy-terminal arginine and lysines from PA20IMPORTANCE Our findings identify a serum-mediated modification of PA20 that has not been previously described. These observations further imply that the processing of PA is more complex than currently thought. Additional study is needed to define the contribution of serum processing of PA to the host response and individual susceptibility to anthrax.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Toxinas Bacterianas / Carboxipeptidasas / Suero / Hidrólisis / Antígenos Bacterianos Tipo de estudio: Prognostic_studies Idioma: En Revista: MSphere Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Toxinas Bacterianas / Carboxipeptidasas / Suero / Hidrólisis / Antígenos Bacterianos Tipo de estudio: Prognostic_studies Idioma: En Revista: MSphere Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos