蛋白质组
生物标志物
镧系元素
仿形(计算机编程)
化学
纳米技术
环境化学
色谱法
计算生物学
材料科学
生物
生物化学
计算机科学
有机化学
离子
操作系统
作者
Shuang Zhang,Zhixiao Xu,Youming Chen,Lai Jiang,Aiting Wang,Guangxia Shen,Xianting Ding
出处
期刊:ACS Nano
[American Chemical Society]
日期:2025-01-22
标识
DOI:10.1021/acsnano.4c12280
摘要
Identifying effective biomarkers has long been a persistent need for early diagnosis and targeted therapy of disease. While mass spectrometry-based label-free proteomics with trace cell has been demonstrated, deep proteomics with ultratrace human biofluid remains challenging due to low protein concentration, extremely limited patient sample volume, and substantial protein contact losses during preprocessing. Herein, we proposed and validated lanthanide metal–organic framework flowers (MOF-flowers), as effective materials, to trap and enrich protein in biofluid jointly through cation−π interaction and O–Ln coordination. We further developed a MOF-flower assisted simplified and single-pot Sample Preparation (Mass-SP) workflow that incorporates protein capture, digest, and peptide elute into one single PCR tube to maximally avoid adsorptive sample loss. We adopted Mass-SP to decipher aqueous humor (AH) proteome signatures from cataract and retinal vein occlusion (RVO) patients and quantified ∼3900 proteins in merely 1 μL of AH. Combined with machine learning, we further identified PFKL as a prioritization biomarker for RVO disease with the areas under the curves of 0.95 ± 0.04. Mass-SP presents a strategy to identify de novo biomarkers and explore potential therapeutic targets with extremely limited clinical human body fluid resources.
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