Division of Infectious Diseases, Department of Medicine, Massachusetts General Hospital, Cambridge, MA 02139, USA.
Sci Transl Med. 2010 Sep 29;2(51):51ps48. doi: 10.1126/scitranslmed.3001612.
As a way of enhancing infections, bacterial pathogens often alter host cell signaling pathways. Here, we describe recent work that highlights a new phosphatase from an intestinal and wound-invading pathogen that manipulates host cell phosphoinositide circuits. Despite the active-site homology between bacterial inositol phosphatases and mammalian phosphatases, sequence differences between them suggest that the development of specific inhibitors may be feasible.
作为增强感染的一种方式,细菌病原体通常会改变宿主细胞的信号通路。在这里,我们描述了最近的一项工作,该工作强调了一种来自肠道和侵袭性伤口病原体的新型磷酸酶,该磷酸酶可以操纵宿主细胞的磷酸肌醇环电路。尽管细菌肌醇磷酸酶和哺乳动物磷酸酶在活性位点上具有同源性,但它们之间的序列差异表明,开发特异性抑制剂可能是可行的。