Panchal Vipul, Brenk Ruth
Department of Biomedicine, University of Bergen, Jonas Lies vei 91, 5020 Bergen, Norway.
Antibiotics (Basel). 2021 Jan 5;10(1):45. doi: 10.3390/antibiotics10010045.
Riboswitches reside in the untranslated region of RNA and regulate genes involved in the biosynthesis of essential metabolites through binding of small molecules. Since their discovery at the beginning of this century, riboswitches have been regarded as potential antibacterial targets. Using fragment screening, high-throughput screening and rational ligand design guided by X-ray crystallography, lead compounds against various riboswitches have been identified. Here, we review the current status and suitability of the thiamine pyrophosphate (TPP), flavin mononucleotide (FMN), , guanine, and other riboswitches as antibacterial targets and discuss them in a biological context. Further, we highlight challenges in riboswitch drug discovery and emphasis the need to develop riboswitch specific high-throughput screening methods.
核糖开关存在于RNA的非翻译区,通过与小分子结合来调控参与必需代谢物生物合成的基因。自本世纪初被发现以来,核糖开关一直被视为潜在的抗菌靶点。通过片段筛选、高通量筛选以及由X射线晶体学指导的合理配体设计,已鉴定出针对各种核糖开关的先导化合物。在此,我们综述了焦磷酸硫胺素(TPP)、黄素单核苷酸(FMN)、鸟嘌呤和其他核糖开关作为抗菌靶点的现状和适用性,并在生物学背景下对其进行讨论。此外,我们强调了核糖开关药物研发中的挑战,并着重指出开发核糖开关特异性高通量筛选方法的必要性。