Centre for Synthesis and Chemical Biology, University College Dublin, Belfield, Dublin 4, Ireland; Department of Molecular Microbiology and Immunology, Bloomberg School of Public Health, The Johns Hopkins University, Baltimore, Maryland 21205.
Department of Molecular Microbiology and Immunology, Bloomberg School of Public Health, The Johns Hopkins University, Baltimore, Maryland 21205.
J Biol Chem. 2020 Mar 27;295(13):4327-4340. doi: 10.1074/jbc.RA119.012251. Epub 2020 Jan 31.
Chemical biology is an emerging field that enables the study and manipulation of biological systems with probes whose reactivities provide structural insights. The opportunistic fungal pathogen possesses a polysaccharide capsule that is a major virulence factor, but is challenging to study. We report here the synthesis of a hydroxylamine-armed fluorescent probe that reacts with reducing glycans and its application to study the architecture of the capsule under a variety of conditions. The probe signal localized intracellularly and at the cell wall-membrane interface, implying the presence of reducing-end glycans at this location where the capsule is attached to the cell body. In contrast, no fluorescence signal was detected in the capsule body. We observed vesicle-like structures containing the reducing-end probe, both intra- and extracellularly, consistent with the importance of vesicles in capsular assembly. Disrupting the capsule with DMSO, ultrasound, or mechanical shear stress resulted in capsule alterations that affected the binding of the probe, as reducing ends were exposed and cell membrane integrity was compromised. Unlike the polysaccharides in the assembled capsule, isolated exopolysaccharides contained reducing ends. The reactivity of the hydroxylamine-armed fluorescent probe suggests a model for capsule assembly whereby reducing ends localize to the cell wall surface, supporting previous findings suggesting that this is an initiation point for capsular assembly. We propose that chemical biology is a promising approach for studying the capsule and its associated polysaccharides to unravel their roles in fungal virulence.
化学生物学是一个新兴领域,它使我们能够使用反应性探针来研究和操纵生物系统,这些探针提供了结构见解。机会性真菌病原体 拥有多糖荚膜,这是主要的毒力因子,但很难研究。我们在这里报告了一种带有羟胺的荧光探针的合成,该探针与还原聚糖反应,并将其应用于在各种条件下研究 荚膜的结构。探针信号在细胞内和细胞壁-膜界面处定位,这意味着在荚膜附着在细胞体的位置存在还原末端聚糖。相比之下,在荚膜体中没有检测到荧光信号。我们观察到含有还原末端探针的囊泡样结构,无论是在细胞内还是细胞外,这与囊泡在荚膜组装中的重要性一致。用 DMSO、超声或机械剪切力破坏荚膜会导致探针结合受到影响,因为还原末端暴露,细胞膜完整性受损。与组装荚膜中的多糖不同,分离的胞外多糖含有还原末端。带有羟胺的荧光探针的反应性表明了一种荚膜组装的模型,其中还原末端定位于细胞壁表面,支持先前的研究结果,表明这是荚膜组装的起始点。我们提出,化学生物学是研究 荚膜及其相关多糖的一种很有前途的方法,可以揭示它们在真菌毒力中的作用。