Vázquez Citlali, Mejia-Tlachi Marlen, González-Chávez Zabdi, Silva Aketzalli, Rodríguez-Zavala José Salud, Moreno-Sánchez Rafael, Saavedra Emma
Departamento de Bioquímica, Instituto Nacional de Cardiología Ignacio Chávez, Mexico city, México.
FEBS Lett. 2017 Dec;591(23):3881-3894. doi: 10.1002/1873-3468.12904. Epub 2017 Nov 27.
Buthionine sulfoximine (BSO) induces decreased glutathione (GSH) and trypanothione [T(SH) ] pools in trypanosomatids, presumably because only gamma-glutamylcysteine synthetase (γECS) is blocked. However, some BSO effects cannot be explained by exclusive γECS inhibition; therefore, its effect on the T(SH) metabolism pathway in Trypanosoma cruzi was re-examined. Parasites exposed to BSO did not synthesize T(SH) even when supplemented with cysteine or GSH, suggesting trypanothione synthetase (TryS) inhibition by BSO. Indeed, recombinant γECS and TryS, but not GSH synthetase, were inhibited by BSO and kinetics and docking analyses on a TcTryS 3D model suggested BSO binding at the GSH site. Furthermore, parasites overexpressing γECS and TryS showed ~ 50% decreased activities after BSO treatment. These results indicated that BSO is also an inhibitor of TryS.
丁硫氨酸亚砜亚胺(BSO)可使锥虫中的谷胱甘肽(GSH)和泛硫乙胺[T(SH)₂]水平降低,推测这是因为只有γ-谷氨酰半胱氨酸合成酶(γECS)被阻断。然而,一些BSO的作用无法仅通过γECS的抑制来解释;因此,重新研究了其对克氏锥虫中T(SH)₂代谢途径的影响。暴露于BSO的寄生虫即使补充半胱氨酸或GSH也不合成T(SH)₂,这表明BSO抑制了泛硫乙胺合成酶(TryS)。事实上,重组γECS和TryS,而非GSH合成酶,受到BSO的抑制,并且对TcTryS三维模型的动力学和对接分析表明BSO在GSH位点结合。此外,过表达γECS和TryS的寄生虫在BSO处理后活性降低了约50%。这些结果表明BSO也是TryS的抑制剂。