Laboratory of Structural Microbiology, Rockefeller University, New York, New York, USA.
Nat Struct Mol Biol. 2010 Jan;17(1):130-2. doi: 10.1038/nsmb.1705. Epub 2009 Dec 6.
The CagA protein of Helicobacter pylori interacts with numerous cellular factors and is associated with increased virulence and risk of gastric carcinoma. We present here the cocrystal structure of a subdomain of CagA with the human kinase PAR1b/MARK2, revealing that a CagA peptide mimics substrates of this kinase family, resembling eukaryotic protein kinase inhibitors. Mutagenesis of conserved residues central to this interaction renders CagA inactive as an inhibitor of MARK2.
幽门螺杆菌的 CagA 蛋白与许多细胞因子相互作用,与增加的毒力和胃癌风险相关。我们在此展示了 CagA 的一个亚结构域与人激酶 PAR1b/MARK2 的共晶结构,揭示了 CagA 肽模拟该激酶家族的底物,类似于真核蛋白激酶抑制剂。对这个相互作用的关键保守残基的突变使 CagA 作为 MARK2 的抑制剂失活。