Li Guanlin, Qu Ye, Cai Chenguang, Kong Yirong, Liu Shuling, Zhang Jun, Zhao Jian, Fu Ling, Xu Junjie, Chen Wei
State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and Epidemiology, Beijing, China.
Biochem Biophys Res Commun. 2009 Aug 7;385(4):591-5. doi: 10.1016/j.bbrc.2009.05.114. Epub 2009 May 30.
The high affinity binding of the anthrax protective antigen (PA) to one of its receptors, capillary morphogenesis protein 2 (CMG2), is essential for the intoxication process of anthrax toxin. To acquire novel research tools to study the PA-CMG2 interaction, we generated several anti-CMG2 monoclonal antibodies (MAbs). We demonstrated that one of the MAbs, 4B5, could inhibit PA-CMG2 binding and could also protect the sensitive cells against an anthrax lethal toxin challenge. We identified the epitope recognized by 4B5 and confirmed that the key residues of the epitope were the residues (119)YI-LK(125) of CMG2. Based on our results, we propose that 4B5 binds to the E122 pocket of CMG2 and interrupts the interaction between the pocket and the PA 2beta3-2beta4 loop. To our knowledge, this is the first report to illustrate that an anti-CMG2 antibody could inhibit the PA-CMG2 interaction and therefore interfere with the intoxication of anthrax toxin.
炭疽保护性抗原(PA)与其受体之一毛细血管形态发生蛋白2(CMG2)的高亲和力结合对于炭疽毒素的中毒过程至关重要。为了获得研究PA-CMG2相互作用的新型研究工具,我们制备了几种抗CMG2单克隆抗体(MAb)。我们证明其中一种单克隆抗体4B5能够抑制PA-CMG2结合,并且还能保护敏感细胞免受炭疽致死毒素攻击。我们鉴定了4B5识别的表位,并确认该表位的关键残基是CMG2的残基(119)YI-LK(125)。基于我们的结果,我们提出4B5与CMG2的E122口袋结合,并中断该口袋与PA 2β3-2β4环之间的相互作用。据我们所知,这是第一份说明抗CMG2抗体能够抑制PA-CMG2相互作用并因此干扰炭疽毒素中毒的报告。