Department of Biology, The Catholic University of America, 620 Michigan Ave, Washington, DC 20064, USA.
Department of Biology, The Catholic University of America, 620 Michigan Ave, Washington, DC 20064, USA.
Biochim Biophys Acta Biomembr. 2021 Nov 1;1863(11):183715. doi: 10.1016/j.bbamem.2021.183715. Epub 2021 Jul 30.
Protective antigen channel is the central component of the deadly anthrax exotoxin responsible for binding and delivery of the toxin's enzymatic lethal and edema factor components into the cytosol. The channel, which is more than three times longer than the lipid bilayer membrane thickness and has a 6-Å limiting diameter, is believed to provide a sophisticated unfoldase and translocase machinery for the foreign protein transport into the host cell cytosol. The tripartite toxin can be reengineered, one component at a time or collectively, to adapt it for the targeted cancer therapeutic treatments. In this review, we focus on the biophysical studies of the protective antigen channel-forming activity, small ion transport properties, enzymatic factor translocation, and blockage comparing it with the related clostridial binary toxin channels. We address issues linked to the anthrax toxin channel structural dynamics and lipid dependence, which are yet to become generally recognized as parts of the toxin translocation machinery.
保护性抗原通道是致命炭疽外毒素的核心组成部分,负责将毒素的酶性致死和水肿因子成分结合并递送至细胞质。该通道的长度超过脂质双层膜厚度的三倍,具有 6-Å 的限制直径,被认为提供了一种复杂的展开酶和转运酶机制,用于将外源蛋白输送到宿主细胞质。三组分毒素可以逐个或集体进行改造,以适应靶向癌症治疗。在这篇综述中,我们专注于保护性抗原通道形成活性、小离子转运特性、酶因子易位和阻断的生物物理研究,并将其与相关梭状芽胞杆菌二元毒素通道进行了比较。我们解决了与炭疽毒素通道结构动力学和脂质依赖性相关的问题,这些问题尚未被普遍认为是毒素易位机制的一部分。