NIBRT GlycoScience Group, National Institute for Bioprocessing, Research and Training, Blackrock, Dublin A94 X099, Ireland.
CÚRAM, SFI Research Centre for Medical Devices, National University of Ireland, Galway, Galway H91 W2TY, Ireland.
J Proteome Res. 2021 Aug 6;20(8):3913-3924. doi: 10.1021/acs.jproteome.1c00219. Epub 2021 Jun 30.
-Glycosylation changes in misfolded proteins are of particular interest in understanding neurodegenerative conditions such as Parkinson's disease (PD) and incidental Lewy body disease (ILBD). This work outlines optimizations of a microwave-assisted release to limit glycan degradation and employs this methodology to analyze -glycosylation on the human striatum and substantia nigra tissue in PD, ILBD, and healthy controls, working alongside well-established release approaches. A total of 70 -glycans were identified, with ILBD presenting significantly decreased levels of mannose-core ( = 0.017) and glucuronylated structures ( = 0.039) in the striatum and PD presenting an increase in sialylation ( < 0.001) and a decrease in sulfation ( = 0.001). Significant increases in sialylation ( = 0.038) in PD were also observed in the substantia nigra. This is the first study to profile the whole nigrostriatal -glycome in healthy, PD, and ILBD tissues, outlining disease biomarkers alongside benefits of employing orthogonal techniques for -glycan analysis.
在理解帕金森病 (PD) 和偶然路易体病 (ILBD) 等神经退行性疾病时,错误折叠蛋白质中的糖基化变化尤其受到关注。本工作概述了微波辅助释放的优化,以限制聚糖降解,并采用这种方法分析 PD、ILBD 和健康对照者的人纹状体和黑质组织中的 - 糖基化,同时采用成熟的 释放方法。共鉴定出 70 种 - 聚糖,ILBD 在纹状体中表现出甘露糖核心 ( = 0.017) 和葡糖醛酸化结构 ( = 0.039) 的显著降低水平,而 PD 则表现出唾液酸化的增加 ( < 0.001) 和硫酸化的减少 ( = 0.001)。在黑质中还观察到 PD 中唾液酸化的显著增加 ( = 0.038)。这是首次在健康、PD 和 ILBD 组织中对整个黑质纹状体 - 聚糖组进行分析的研究,概述了疾病生物标志物,并展示了采用正交技术进行 - 聚糖分析的益处。