Pinto Torres Joar Esteban, Claes Mathieu, Hendrickx Rik, Yuan Meng, Smiejkowska Natalia, Van Wielendaele Pieter, Hacisuleyman Aysima, De Winter Hans, Muyldermans Serge, Michels Paul A M, Walkinshaw Malcolm D, Versées Wim, Caljon Guy, Magez Stefan, Sterckx Yann G-J
Laboratory for Cellular and Molecular Immunology (CMIM), Vrije Universiteit Brussel (VUB), Brussel, Belgium.
Laboratory of Microbiology, Parasitology and Hygiene (LMPH) and the Infla-Med Centre of Excellence, University of Antwerp, Wilrijk, Belgium.
Elife. 2025 Mar 31;13:RP100066. doi: 10.7554/eLife.100066.
African trypanosomes are the causative agents of neglected tropical diseases affecting both humans and livestock. Disease control is highly challenging due to an increasing number of drug treatment failures. African trypanosomes are extracellular, blood-borne parasites that mainly rely on glycolysis for their energy metabolism within the mammalian host. Trypanosomal glycolytic enzymes are therefore of interest for the development of trypanocidal drugs. Here, we report the serendipitous discovery of a camelid single-domain antibody (sdAb aka Nanobody) that selectively inhibits the enzymatic activity of trypanosomatid (but not host) pyruvate kinases through an allosteric mechanism. By combining enzyme kinetics, biophysics, structural biology, and transgenic parasite survival assays, we provide a proof-of-principle that the sdAb-mediated enzyme inhibition negatively impacts parasite fitness and growth.
非洲锥虫是影响人类和牲畜的被忽视热带病的病原体。由于药物治疗失败的案例不断增加,疾病控制极具挑战性。非洲锥虫是细胞外的血源寄生虫,在哺乳动物宿主体内主要依靠糖酵解进行能量代谢。因此,锥虫糖酵解酶是开发杀锥虫药物的关注对象。在此,我们报告了一项意外发现:一种骆驼科单域抗体(sdAb,又名纳米抗体)通过变构机制选择性抑制锥虫(而非宿主)丙酮酸激酶的酶活性。通过结合酶动力学、生物物理学、结构生物学和转基因寄生虫存活试验,我们提供了原理证明,即sdAb介导的酶抑制对寄生虫的适应性和生长产生负面影响。