Kumbalathara A D Umesha Subhani S, Bartolomeu Halicki Priscila Cristina, Kalera Karishma, Swarts Benjamin M, Rohde Kyle H, Sucheck Steven J
Department of Chemistry and Biochemistry, University of Toledo, Toledo, OH, 43606, United States.
Division of Immunity and Pathogenesis, Burnett School of Biomedical Sciences, College of Medicine, University of Central Florida, Orlando, FL, 32827, United States.
Carbohydr Res. 2025 Jul;553:109506. doi: 10.1016/j.carres.2025.109506. Epub 2025 May 3.
One obstacle to developing new drugs targeting Mycobacterium tuberculosis (Mtb) is its unique cell wall, which forms a significant permeability barrier to drug transport. Recently, transporters of trehalose and other disaccharides within this structure have been identified. We hypothesized that conjugating small molecules active against Mtb with trehalose could facilitate selective uptake of the trehalose conjugate into the cell. This strategy might enhance penetration of the hydrophobic mycomembrane or enable selective targeting of mycobacteria. To test this hypothesis, we used Cu(I)-catalyzed azide-alkyne Huisgen cycloaddition to conjugate 6-azido trehalose to known polyketide synthase 13 (Pks13) inhibitors, such as 2-aminothiophenes (AT), and benzofurans (BzF) with alkyne moieties, and tested the conjugates' activity against mycobacteria. We found that, in some instances, trehalose served to significantly enhance either the antimycobacterial potency or improve selectivity (by reducing toxicity) of the Pks13 inhibitors. Somewhat surprisingly, in M. smegmatis (Msm), the activity of trehalose-modified AT derivatives was independent of the trehalose transporter LpqY-SugABC, suggesting an alternative mechanism(s) of passage into the cell. Thus, the mechanisms underlying trehalose-enhanced inhibitor activity remains to be elucidated. Future studies applying this Trojan Horse strategy to alternative inhibitor chemotypes will be needed to assess the potential of this approach to overcoming the mycomembrane permeability barrier.
开发针对结核分枝杆菌(Mtb)的新药的一个障碍是其独特的细胞壁,它对药物转运形成了显著的渗透屏障。最近,已在该结构中鉴定出海藻糖和其他二糖的转运体。我们假设将对Mtb有活性的小分子与海藻糖缀合可以促进海藻糖缀合物选择性摄取到细胞中。这种策略可能会增强疏水的分枝菌膜的渗透性,或者实现对分枝杆菌的选择性靶向。为了验证这一假设,我们使用铜(I)催化的叠氮化物-炔烃惠斯根环加成反应,将6-叠氮基海藻糖与已知的聚酮合酶13(Pks13)抑制剂缀合,如带有炔基部分的2-氨基噻吩(AT)和苯并呋喃(BzF),并测试了这些缀合物对分枝杆菌的活性。我们发现,在某些情况下,海藻糖可显著增强Pks13抑制剂的抗分枝杆菌效力或提高其选择性(通过降低毒性)。有点令人惊讶的是,在耻垢分枝杆菌(Msm)中,海藻糖修饰的AT衍生物的活性与海藻糖转运体LpqY-SugABC无关,这表明存在进入细胞的替代机制。因此,海藻糖增强抑制剂活性的潜在机制仍有待阐明。未来需要将这种特洛伊木马策略应用于其他抑制剂化学类型的研究,以评估这种方法克服分枝菌膜渗透屏障的潜力。