骆驼单域抗体对丙酮酸锥虫激酶的变构抑制作用。

IF 6.4 1区 生物学 Q1 BIOLOGY
eLife Pub Date : 2025-03-31 DOI:10.7554/eLife.100066
Joar Esteban Pinto Torres, Mathieu Claes, Rik Hendrickx, Meng Yuan, Natalia Smiejkowska, Pieter Van Wielendaele, Aysima Hacisuleyman, Hans De Winter, Serge Muyldermans, Paul A M Michels, Malcolm D Walkinshaw, Wim Versées, Guy Caljon, Stefan Magez, Yann G-J Sterckx
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引用次数: 0

摘要

非洲锥虫是影响人类和牲畜的被忽视的热带病的病原体。由于越来越多的药物治疗失败,疾病控制极具挑战性。非洲锥虫是细胞外血源性寄生虫,主要依靠糖酵解在哺乳动物宿主体内进行能量代谢。因此,锥虫体糖酵解酶对锥虫药物的开发具有重要意义。在这里,我们报告了偶然发现的一种骆驼单域抗体(sdAb又称纳米体),它通过变构机制选择性地抑制锥虫虫(但不是宿主)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分析,我们提供了sdab介导的酶抑制对寄生虫适应性和生长产生负面影响的原理证明。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Allosteric inhibition of trypanosomatid pyruvate kinases by a camelid single-domain antibody.

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.

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来源期刊
eLife
eLife BIOLOGY-
CiteScore
12.90
自引率
3.90%
发文量
3122
审稿时长
17 weeks
期刊介绍: eLife is a distinguished, not-for-profit, peer-reviewed open access scientific journal that specializes in the fields of biomedical and life sciences. eLife is known for its selective publication process, which includes a variety of article types such as: Research Articles: Detailed reports of original research findings. Short Reports: Concise presentations of significant findings that do not warrant a full-length research article. Tools and Resources: Descriptions of new tools, technologies, or resources that facilitate scientific research. Research Advances: Brief reports on significant scientific advancements that have immediate implications for the field. Scientific Correspondence: Short communications that comment on or provide additional information related to published articles. Review Articles: Comprehensive overviews of a specific topic or field within the life sciences.
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