质谱法
生物标志物发现
生物分析
生物标志物
肽
2019年冠状病毒病(COVID-19)
蛋白质组学
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
化学
计算生物学
色谱法
医学
生物
疾病
内科学
生物化学
传染病(医学专业)
基因
作者
Bart Van Puyvelde,Christie L. Hunter,Maxim Zhgamadze,Sudha S. Savant,Y. Wang,Esthelle Hoedt,Koen Raedschelders,Matt Pope,Carissa A. Huynh,V. Krishnan Ramanujan,Warren G. Tourtellotte,Morteza Razavi,N. Leigh Anderson,Geert A. Martens,Dieter Deforce,Qin Fu,Maarten Dhaenens,Jennifer E. Van Eyk
标识
DOI:10.1038/s41467-024-48563-z
摘要
Abstract The global scientific response to COVID 19 highlighted the urgent need for increased throughput and capacity in bioanalytical laboratories, especially for the precise quantification of proteins that pertain to health and disease. Acoustic ejection mass spectrometry (AEMS) represents a much-needed paradigm shift for ultra-fast biomarker screening. Here, a quantitative AEMS assays is presented, employing peptide immunocapture to enrich (i) 10 acute phase response (APR) protein markers from plasma, and (ii) SARS-CoV-2 NCAP peptides from nasopharyngeal swabs. The APR proteins were quantified in 267 plasma samples, in triplicate in 4.8 h, with %CV from 4.2% to 10.5%. SARS-CoV-2 peptides were quantified in triplicate from 145 viral swabs in 10 min. This assay represents a 15-fold speed improvement over LC-MS, with instrument stability demonstrated across 10,000 peptide measurements. The combination of speed from AEMS and selectivity from peptide immunocapture enables ultra-high throughput, reproducible quantitative biomarker screening in very large cohorts.
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