Helmholtz Institute for Pharmaceutical Research Saarland (HIPS) - Helmholtz Centre for Infection Research (HZI), Department of Drug Design and Optimization, Saarbrücken, Germany.
Saarland University, Department of Pharmacy, Saarbrücken, Germany.
Protein Sci. 2024 Nov;33(11):e5195. doi: 10.1002/pro.5195.
This study investigates the potential of energy-coupling factor (ECF) transporters as promising anti-infective targets to combat antimicrobial resistance (AMR). ECF transporters, a subclass of ATP-binding cassette (ABC) transporters, facilitate the uptake of B-vitamins across bacterial membranes by utilizing ATP as an energy source. Vitamins are essential cofactors for bacterial metabolism and growth, and they can either be synthesized de novo or absorbed from the environment. These transporters are considered promising drug targets, underscoring the need for further research to harness their medicinal potential and develop selective inhibitors that block vitamin uptake in bacteria. Herein, we focused on the ECF transporter for pantothenate (vitamin B5) from Streptococcus pneumoniae and the ECF transporter for folate (vitamin B9) from Lactobacillus delbrueckii as a reference protein. We also included the energizing module for pantothenate along with both full transporter complexes. Initially, we transformed and purified the transporters, followed by an assessment of their thermal stability under various buffer composition, pH, and salt concentrations. Additionally, we monitored the melting temperature over six days to confirm their stability for further assays. We then measured the binding affinities of six ECF inhibitors using surface plasmon resonance (SPR) and evaluated their inhibitory effects through in vitro assays, including bacterial growth assay, whole-cell uptake, and transport-activity assays. After determining cytotoxicity in two human cell lines, we established an in vivo infection model using Galleria mellonella larvae to further validate our findings.
本研究探讨了能量偶联因子(ECF)转运蛋白作为有前途的抗微生物药物靶点,以对抗抗菌药物耐药性(AMR)。ECF 转运蛋白是 ATP 结合盒(ABC)转运蛋白的一个亚类,通过利用 ATP 作为能量来源,促进细菌细胞膜内外 B 族维生素的摄取。维生素是细菌代谢和生长所必需的辅酶,它们可以从头合成或从环境中吸收。这些转运蛋白被认为是有前途的药物靶点,这突显了进一步研究它们的药用潜力并开发选择性抑制剂以阻断细菌中维生素摄取的必要性。在此,我们专注于肺炎链球菌的泛酸(维生素 B5)ECF 转运蛋白和德氏乳杆菌的叶酸(维生素 B9)ECF 转运蛋白作为参考蛋白。我们还包括泛酸的供能模块以及完整的转运蛋白复合物。最初,我们对转运蛋白进行转化和纯化,然后在不同的缓冲液组成、pH 值和盐浓度下评估它们的热稳定性。此外,我们还监测了六天的熔点以确认它们的稳定性,以便进行进一步的测定。然后,我们使用表面等离子体共振(SPR)测量了六种 ECF 抑制剂的结合亲和力,并通过体外测定评估了它们的抑制作用,包括细菌生长测定、全细胞摄取和转运活性测定。在确定了两种人类细胞系中的细胞毒性后,我们使用家蚕幼虫建立了体内感染模型,以进一步验证我们的发现。