恰加斯病
拓扑异构酶
锥虫病
药品
生物
非洲锥虫病
疾病
中止
杀锥虫剂
克鲁兹锥虫
苯硝唑
病毒学
药理学
免疫学
医学
布氏锥虫
体外
寄生虫寄主
内科学
遗传学
基因
万维网
计算机科学
作者
Srinivasa P. S. Rao,Matthew K. Gould,J. Noeske,Manuel Saldivia,Rajiv S. Jumani,Pearly Shuyi Ng,Olivier René,Yen‐Liang Chen,Marcel Kaiser,Ryan Ritchie,Amanda Fortes Francisco,Nila Johnson,Debjani Patra,H. W. K. Cheung,Colin Deniston,Andreas D. Schenk,Wilian A. Cortopassi,Remo S. Schmidt,Natalie Wiedemar,Bryanna Thomas
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2023-06-29
卷期号:380 (6652): 1349-1356
被引量:24
标识
DOI:10.1126/science.adh0614
摘要
Millions who live in Latin America and sub-Saharan Africa are at risk of trypanosomatid infections, which cause Chagas disease and human African trypanosomiasis (HAT). Improved HAT treatments are available, but Chagas disease therapies rely on two nitroheterocycles, which suffer from lengthy drug regimens and safety concerns that cause frequent treatment discontinuation. We performed phenotypic screening against trypanosomes and identified a class of cyanotriazoles (CTs) with potent trypanocidal activity both in vitro and in mouse models of Chagas disease and HAT. Cryo-electron microscopy approaches confirmed that CT compounds acted through selective, irreversible inhibition of trypanosomal topoisomerase II by stabilizing double-stranded DNA:enzyme cleavage complexes. These findings suggest a potential approach toward successful therapeutics for the treatment of Chagas disease.
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