Serum-Mediated Cleavage ofBacillus anthracisProtective Antigen Is a Two-Step Process That Involves a Serum Carboxypeptidase
ABSTRACTMuch of our understanding of the activity of anthrax toxin is based onin vitrosystems, which delineate the interaction betweenBacillus anthracistoxins and the cell surface. However, these systems fail to account for the intimate association ofB. anthraciswith 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 ofB. anthracisprotective antigen (PA) along with mass spectrometry analysis, we demonstrate that serum digests PA via 2 distinct reactions. In the first reaction, serum cleaves PA83into 2 fragments to produce PA63and PA20fragments, similarly to that observed following furin digestion. This is followed by carboxypeptidase-mediated removal of the carboxy-terminal arginine and lysines from PA20.IMPORTANCEOur findings identify a serum-mediated modification of PA20that 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.