Camperi Silvia A, Acosta Gerardo, Barredo Gabriela R, Iglesias-García Lucía C, Alves da Silva Caldeira Cleópatra, Martínez-Ceron María C, Giudicessi Silvana L, Cascone Osvaldo, Albericio Fernando
Universidad de Buenos Aires, Facultad de Farmacia y Bioquímica, Cátedra de Biotecnología, Junín 956, 1113, Buenos Aires, Argentina.
CONICET-Universidad de Buenos Aires, Instituto de Nanobiotecnología (NANOBIOTEC), Facultad de Farmacia y Bioquímica, Junín 956, 1113, Buenos Aires, Argentina.
Toxicon X. 2020 May 5;6:100038. doi: 10.1016/j.toxcx.2020.100038. eCollection 2020 Jun.
Scorpion and spider envenomation is treated with the appropriate antivenoms, prepared as described by Césaire Auguste Phisalix and Albert Calmette in 1894. Such treatment requires the acquisition and manipulation of arachnid venoms, both very complicated procedures. Most of the toxins in the venoms of spiders and scorpions are extremely stable cysteine-rich peptide neurotoxins. Many strategies have been developed to obtain synthetic immunogens to facilitate the production of antivenoms against these toxins. For example, whole peptide toxins can be synthesized by solid-phase peptide synthesis (SPPS). Also, epitopes of the toxins can be identified and after the chemical synthesis of these peptide epitopes by SPPS, they can be coupled to protein carriers to develop efficient immunogens. Moreover, multiple antigenic peptides with a polylysine core can be designed and synthesized. This review focuses on the strategies developed to obtain synthetic immunogens for the production of antivenoms against the toxic Cys-rich peptides of scorpions and spiders.
蝎子和蜘蛛蜇伤可用适当的抗蛇毒血清治疗,这些抗蛇毒血清是按照塞泽尔·奥古斯特·菲萨利克斯和阿尔贝·卡尔梅特在1894年所描述的方法制备的。这种治疗需要获取和处理蛛形纲动物毒液,这两个过程都非常复杂。蜘蛛和蝎子毒液中的大多数毒素都是极其稳定的富含半胱氨酸的肽类神经毒素。人们已经开发出许多策略来获得合成免疫原,以促进针对这些毒素的抗蛇毒血清的生产。例如,全肽毒素可以通过固相肽合成(SPPS)来合成。此外,可以鉴定毒素的表位,在通过SPPS化学合成这些肽表位后,可将它们与蛋白质载体偶联以开发高效免疫原。而且,可以设计并合成具有聚赖氨酸核心的多抗原肽。本综述重点关注为生产针对蝎子和蜘蛛有毒富含半胱氨酸肽的抗蛇毒血清而开发的获取合成免疫原的策略。