Mutschler Hannes, Reinstein Jochen, Meinhart Anton
Department of Biomolecular Mechanisms, Max Planck Institute for Medical Research, 69120 Heidelberg, Germany.
J Biol Chem. 2010 Jul 9;285(28):21797-806. doi: 10.1074/jbc.M110.126250. Epub 2010 May 4.
The pneumococcal epsilon zeta antitoxin toxin (PezAT) system is a chromosomally encoded, class II toxin antitoxin system from the human pathogen Streptococcus pneumnoniae. Neutralization of the bacteriotoxic protein PezT is carried out by complex formation with its cognate antitoxin PezA. Here we study the stability of the inhibitory complex in vivo and in vitro. We found that toxin release is impeded in Escherichia coli and Bacillus subtilis due to the proteolytic resistance of PezA once bound to PezT. These findings are supported by in vitro experiments demonstrating a strong thermodynamic stabilization of both proteins upon binding. A detailed kinetic analysis of PezAT assembly revealed that these particular features of PezAT are based on a strong, electrostatically guided binding mechanism leading to a stable toxin antitoxin complex with femtomolar affinity. Our data show that PezAT complex formation is distinct to all other conventional toxin antitoxin modules and a controlled mode of toxin release is required for activation.
肺炎链球菌εζ抗毒素毒素(PezAT)系统是一种由人类病原体肺炎链球菌染色体编码的II类毒素-抗毒素系统。细菌毒性蛋白PezT通过与其同源抗毒素PezA形成复合物来实现中和作用。在此,我们研究了抑制性复合物在体内和体外的稳定性。我们发现,由于PezA一旦与PezT结合就具有蛋白水解抗性,因此在大肠杆菌和枯草芽孢杆菌中,毒素的释放受到阻碍。体外实验表明,两种蛋白质结合后具有很强的热力学稳定性,这支持了上述发现。对PezAT组装的详细动力学分析表明,PezAT的这些特殊特征基于一种强大的、静电引导的结合机制,该机制导致形成具有飞摩尔亲和力的稳定毒素-抗毒素复合物。我们的数据表明,PezAT复合物的形成与所有其他传统毒素-抗毒素模块不同,并且激活需要一种受控的毒素释放模式。