Advances in aqueous humor proteomics for biomarker discovery and disease mechanisms exploration: a spotlight on primary open angle glaucoma

V. M. Beutgen, Johannes Graumann
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Abstract

Altered protein levels in the aqueous humor (AH) may be a valuable source of novel biomarkers in neurodegenerative retinal disease. The proximity of this body fluid to the disease focus, and its corresponding enrichment for tissue specific proteins, renders it an excellent matrix to study underlying molecular mechanisms. Novel proteomic methods accordingly hold large potential for insight into pathologies based on the composition of the AH proteome, including primary open angle glaucoma (POAG). Recent mass spectrometry-based studies use novel approaches to tackle the challenges arising from the combination of low available sample volume and protein concentration, thereby increasing proteome coverage. But despite significant improvements in mass spectrometry (MS), a different class of proteomic technologies is poised to majorly impact the analysis of ocular biofluids. Affinity proteomic workflows, having become available commercially recently, have started to complement data obtained by MS and likely will grow into a crucial tool for ophthalmological biomarker research. This review highlights corresponding approaches in proteome analysis of aqueous humor and discusses recent findings on alterations of the AH proteome in POAG.
用于生物标记物发现和疾病机制探索的眼液蛋白质组学研究进展:聚焦原发性开角型青光眼
房水(AH)中蛋白质水平的改变可能是神经退行性视网膜疾病新型生物标志物的重要来源。这种体液接近病灶,相应地富含组织特异性蛋白质,因此是研究潜在分子机制的绝佳基质。因此,新的蛋白质组学方法具有很大的潜力,可根据 AH 蛋白质组的组成深入了解病理,包括原发性开角型青光眼(POAG)。近期基于质谱的研究采用了新型方法来解决因样本量少和蛋白质浓度低而带来的挑战,从而提高了蛋白质组的覆盖率。不过,尽管质谱技术(MS)有了长足的进步,但另一类蛋白质组学技术将对眼部生物流体的分析产生重大影响。亲和蛋白组学工作流程最近开始商业化,开始对质谱获得的数据进行补充,并有可能发展成为眼科生物标志物研究的重要工具。本综述重点介绍了对房水进行蛋白质组分析的相应方法,并讨论了有关 POAG 患者房水蛋白质组变化的最新发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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