School of Biochemistry, University of Bristol, University Walk, Bristol BS8 1TD, United Kingdom.
Biochemistry. 2024 Sep 17;63(18):2344-2351. doi: 10.1021/acs.biochem.4c00264. Epub 2024 Aug 29.
There is a pressing need for new antibiotics to combat rising resistance to those already in use. The bacterial general secretion (Sec) system has long been considered a good target for novel antimicrobials thanks to its irreplacable role in maintaining cell envelope integrity, yet the lack of a robust, high-throughput method to screen for Sec inhibition has so far hampered efforts to realize this potential. Here, we have adapted our recently developed assay for Sec activity─based on the split NanoLuc luciferase─to work at scale and in living cells. A simple counterscreen allows compounds that specifically target Sec to be distinguished from those with other effects on cellular function. As proof of principle, we have applied this assay to a library of 5000 compounds and identified a handful of moderately effective inhibitors of Sec. Although these hits are unlikely to be potent enough to use as a basis for drug development, they demonstrate the efficacy of the screen. We therefore anticipate that the methods presented here will be scalable to larger compound libraries, in the ultimate quest for Sec inhibitors with clinically relevant properties.
迫切需要新的抗生素来对抗现有抗生素耐药性的上升。细菌普遍分泌(Sec)系统因其在维持细胞包膜完整性方面不可替代的作用,长期以来一直被认为是新型抗菌药物的一个很好的靶点,但缺乏一种强大的高通量筛选 Sec 抑制的方法,这使得实现这一潜力的努力受到了阻碍。在这里,我们对我们最近开发的基于 Sec 活性的纳米荧光素酶(split NanoLuc luciferase)的检测方法进行了改编,使其能够在大规模和活细胞中工作。一个简单的反筛选可以将专门针对 Sec 的化合物与那些对细胞功能有其他影响的化合物区分开来。作为原理验证,我们将该检测方法应用于 5000 种化合物库,并鉴定出了一小部分具有中等抑制 Sec 活性的抑制剂。尽管这些化合物不太可能具有足够的效力作为药物开发的基础,但它们证明了该筛选的有效性。因此,我们预计这里提出的方法可以扩展到更大的化合物库,最终寻求具有临床相关特性的 Sec 抑制剂。