聚糖
生物标志物发现
纳米医学
纳米技术
糖蛋白
糖基化
纤维蛋白原
计算生物学
蛋白质组学
生物标志物
仿形(计算机编程)
纳米颗粒
糖组
化学
材料科学
生物
计算机科学
生物化学
基因
操作系统
作者
Duong N. Trinh,Richard A. Gardner,Alessandro N. Franciosi,Cormac McCarthy,Michael P. Keane,Mahmoud G. Soliman,James S. O’Donnell,Paula Meleady,Daniel I. R. Spencer,Marco P. Monopoli
出处
期刊:ACS Nano
[American Chemical Society]
日期:2022-03-28
卷期号:16 (4): 5463-5475
被引量:44
标识
DOI:10.1021/acsnano.1c09564
摘要
Biomolecular corona formation has emerged as a recurring and important phenomenon in nanomedicine that has been investigated for potential applications in disease diagnosis. In this study, we have combined the "personalized protein corona" with the N-glycosylation profiling that has recently gained considerable interest in human plasma biomarker discovery as a powerful early warning diagnostic and patient stratification tool. We envisioned that the protein corona formation could be exploited as an enrichment step that is critically important in both proteomic and proteoglycomic workflows. By using silica nanoparticles, plasma fibrinogen was enriched to a level in which its proteomic and glycomic "fingerprints" could be traced with confidence. Despite being a more simplified glycan profile compared to full plasma, the corona glycan profile revealed a fibrinogen-derived glycan peak that was found to potentially distinguish lung cancer patients from controls in a pilot study.
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