Department of Biochemistry, Indian Institute of Science, Bangalore, Karnataka, India.
PLoS One. 2013 Jul 29;8(7):e70273. doi: 10.1371/journal.pone.0070273. Print 2013.
Abrin, an A/B toxin obtained from the Abrus precatorius plant is extremely toxic and a potential bio-warfare agent. Till date there is no antidote or vaccine available against this toxin. The only known neutralizing monoclonal antibody against abrin, namely D6F10, has been shown to rescue the toxicity of abrin in cells as well as in mice. The present study focuses on mapping the epitopic region to understand the mechanism of neutralization of abrin by the antibody D6F10. Truncation and mutational analysis of abrin A chain revealed that the amino acids 74-123 of abrin A chain contain the core epitope and the residues Thr112, Gly114 and Arg118 are crucial for binding of the antibody. In silico analysis of the position of the mapped epitope indicated that it is present close to the active site cleft of abrin A chain. Thus, binding of the antibody near the active site blocks the enzymatic activity of abrin A chain, thereby rescuing inhibition of protein synthesis by the toxin in vitro. At 1∶10 molar concentration of abrin:antibody, the antibody D6F10 rescued cells from abrin-mediated inhibition of protein synthesis but did not prevent cell attachment of abrin. Further, internalization of the antibody bound to abrin was observed in cells by confocal microscopy. This is a novel finding which suggests that the antibody might function intracellularly and possibly explains the rescue of abrin's toxicity by the antibody in whole cells and animals. To our knowledge, this study is the first report on a neutralizing epitope for abrin and provides mechanistic insights into the poorly understood mode of action of anti-A chain antibodies against several toxins including ricin.
相思豆毒素 Abrin 是从相思豆植物中提取的 A/B 型毒素,具有很强的毒性,是一种潜在的生物战剂。迄今为止,尚无针对这种毒素的解毒剂或疫苗。目前已知的抗 Abrin 的中和单克隆抗体是 D6F10,它已被证明可以在细胞中和小鼠中挽救 Abrin 的毒性。本研究集中于绘制表位区域,以了解抗体 D6F10 中和 Abrin 的机制。 Abrin A 链的截断和突变分析表明,Abrin A 链的 74-123 个氨基酸含有核心表位,而 Thr112、Gly114 和 Arg118 残基对于抗体的结合至关重要。对映射表位位置的计算分析表明,它位于 Abrin A 链的活性位点裂缝附近。因此,抗体在靠近活性位点的位置结合会阻止 Abrin A 链的酶活性,从而在体外挽救毒素对蛋白质合成的抑制作用。在 Abrin:抗体摩尔浓度为 1∶10 时,抗体 D6F10 可挽救细胞免受 Abrin 介导的蛋白质合成抑制,但不能阻止 Abrin 与细胞的附着。此外,通过共聚焦显微镜观察到与 Abrin 结合的抗体在细胞内内化。这是一个新的发现,表明该抗体可能在细胞内发挥作用,并可能解释抗体在整个细胞和动物中挽救 Abrin 毒性的原因。据我们所知,这项研究是针对 Abrin 的中和表位的首次报道,并为抗 A 链抗体针对包括蓖麻毒素在内的几种毒素的作用机制提供了深入的了解。