Department of Chemistry, The Pennsylvania State University, University Park, PA, 16802, USA.
Department of Biochemistry and Molecular Biology, The Pennsylvania State University, University Park, PA, 16802, USA.
Angew Chem Int Ed Engl. 2017 Jul 17;56(30):8672-8676. doi: 10.1002/anie.201702417. Epub 2017 Jun 19.
Drug-induced proteome stress that involves protein aggregation may cause adverse effects and undermine the safety profile of a drug. Safety of drugs is regularly evaluated using cytotoxicity assays that measure cell death. However, these assays provide limited insights into the presence of proteome stress in live cells. A fluorogenic protein sensor is reported to detect drug-induced proteome stress prior to cell death. An aggregation prone Halo-tag mutant (AgHalo) was evolved to sense proteome stress through its aggregation. Detection of such conformational changes was enabled by a fluorogenic ligand that fluoresces upon AgHalo forming soluble aggregates. Using 5 common anticancer drugs, we exemplified detection of differential proteome stress before any cell death was observed. Thus, this sensor can be used to evaluate drug safety in a regime that the current cytotoxicity assays cannot cover and be generally applied to detect proteome stress induced by other toxins.
药物诱导的蛋白质组应激,包括蛋白质聚集,可能会导致不良反应,并破坏药物的安全性。药物的安全性通常通过细胞毒性测定来评估,该测定方法可测量细胞死亡。然而,这些测定方法提供的关于活细胞中蛋白质组应激存在的信息有限。荧光蛋白传感器可用于在细胞死亡之前检测药物诱导的蛋白质组应激。通过其聚集,一种易于聚集的 Halo 标签突变体(AgHalo)被进化为感知蛋白质组应激。通过荧光配体来实现对这种构象变化的检测,当 AgHalo 形成可溶性聚集体时,该配体就会发出荧光。使用 5 种常见的抗癌药物,我们举例说明了在观察到任何细胞死亡之前,对差异蛋白质组应激的检测。因此,这种传感器可用于评估当前细胞毒性测定无法涵盖的药物安全性,并可普遍用于检测其他毒素引起的蛋白质组应激。