ProGenTomics, Laboratory of Pharmaceutical Biotechnology, Ghent University, 9000, Ghent, Belgium.
Advanced Clinical Biosystems Research Institute, Smidt Heart Institute, Cedars-Sinai Medical Center, Los Angeles, CA, 90048, USA.
Nat Commun. 2024 Jun 15;15(1):5114. doi: 10.1038/s41467-024-48563-z.
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.
全球科学界对 COVID-19 的应对凸显了生物分析实验室提高通量和容量的迫切需求,特别是对与健康和疾病相关的蛋白质进行精确定量。声喷射质谱 (AEMS) 代表了超快速生物标志物筛选急需的范式转变。在这里,提出了一种定量 AEMS 测定法,该方法采用肽免疫捕获来富集 (i) 来自血浆的 10 种急性相反应 (APR) 蛋白标志物,和 (ii) 鼻咽拭子中的 SARS-CoV-2 NCAP 肽。在 267 个血浆样本中重复测量 3 次,在 4.8 小时内完成,CV% 为 4.2% 至 10.5%。从 145 个病毒拭子中重复测量 3 次,耗时 10 分钟即可定量 SARS-CoV-2 肽。与 LC-MS 相比,该测定法的速度提高了 15 倍,在进行 10000 次肽测量时显示出仪器稳定性。AEMS 的速度和肽免疫捕获的选择性相结合,使在非常大的队列中进行超高通量、可重复的定量生物标志物筛选成为可能。