Department of Bacteriology, Graduate School of Medical Sciences, Kanazawa University, Ishikawa, Japan.
Department of Forensic Medicine and Pathology, Graduate School of Medical Sciences, Kanazawa University, Ishikawa, Japan.
Methods Mol Biol. 2020;2132:183-190. doi: 10.1007/978-1-0716-0430-4_19.
Botulinum hemagglutinin (HA) is one of the auxiliary protein components of the botulinum neurotoxin (BoNT) complex, the most lethal toxin known. HA promotes the intestinal absorption of BoNT by at least two mechanisms, resulting in high oral toxicity. One of the mechanisms is the attachment of large progenitor toxin complexes (L-PTCs) to the cell surface of the intestinal epithelium by the carbohydrate-binding activity of HA. The other is epithelial barrier disruption by the E-cadherin-binding activity of HA. The carbohydrate-binding activity of HA also promotes attachment to the basolateral cell surface, which increases the frequency of contact between HA and E-cadherin. Together, the carbohydrate-binding activity of HA is critical for the intestinal absorption of BoNTs. The trimeric triskelion-shaped structure of HA confers the multivalent binding to its ligands and increases the pathogenic biological activities of HA.
肉毒梭菌血凝素(HA)是肉毒神经毒素(BoNT)复合物的辅助蛋白成分之一,是已知最致命的毒素。HA 通过至少两种机制促进 BoNT 的肠道吸收,导致高口服毒性。其中一种机制是通过 HA 的碳水化合物结合活性将大前体毒素复合物(L-PTC)附着到肠上皮细胞的表面。另一种机制是 HA 的 E-钙黏蛋白结合活性破坏上皮屏障。HA 的碳水化合物结合活性还促进与基底外侧细胞表面的附着,从而增加 HA 与 E-钙黏蛋白接触的频率。HA 的碳水化合物结合活性对于 BoNTs 的肠道吸收至关重要。HA 的三聚体三链体结构赋予其对配体的多价结合,并增加了 HA 的致病生物学活性。