Science for Life Laboratory, Solna, Sweden.
The Royal Institute of Technology, Division of Systems Biology, Department of Protein Science, School of Chemistry, Biotechnology and Health, Stockholm, Sweden.
Elife. 2021 Nov 8;10:e70843. doi: 10.7554/eLife.70843.
Reliable, robust, large-scale molecular testing for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is essential for monitoring the ongoing coronavirus disease 2019 (COVID-19) pandemic. We have developed a scalable analytical approach to detect viral proteins based on peptide immuno-affinity enrichment combined with liquid chromatography-mass spectrometry (LC-MS). This is a multiplexed strategy, based on targeted proteomics analysis and read-out by LC-MS, capable of precisely quantifying and confirming the presence of SARS-CoV-2 in phosphate-buffered saline (PBS) swab media from combined throat/nasopharynx/saliva samples. The results reveal that the levels of SARS-CoV-2 measured by LC-MS correlate well with their correspondingreal-time polymerase chain reaction (RT-PCR) read-out (r = 0.79). The analytical workflow shows similar turnaround times as regular RT-PCR instrumentation with a quantitative read-out of viral proteins corresponding to cycle thresholds (Ct) equivalents ranging from 21 to 34. Using RT-PCR as a reference, we demonstrate that the LC-MS-based method has 100% negative percent agreement (estimated specificity) and 95% positive percent agreement (estimated sensitivity) when analyzing clinical samples collected from asymptomatic individuals with a Ct within the limit of detection of the mass spectrometer (Ct ≤ 30). These results suggest that a scalable analytical method based on LC-MS has a place in future pandemic preparedness centers to complement current virus detection technologies.
可靠、稳健、大规模的严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)分子检测对于监测正在进行的 2019 年冠状病毒病(COVID-19)大流行至关重要。我们已经开发了一种基于肽免疫亲和富集结合液相色谱-质谱(LC-MS)的可扩展分析方法来检测病毒蛋白。这是一种基于靶向蛋白质组学分析和 LC-MS 读出的多重策略,能够精确定量和确认磷酸盐缓冲盐水(PBS)拭子介质中 SARS-CoV-2 的存在,这些拭子来自联合的喉咙/鼻咽/唾液样本。结果表明,LC-MS 测量的 SARS-CoV-2 水平与实时聚合酶链反应(RT-PCR)读数很好地相关(r = 0.79)。分析工作流程与常规 RT-PCR 仪器具有相似的周转时间,具有与循环阈值(Ct)等效物相对应的病毒蛋白的定量读数,范围从 21 到 34。使用 RT-PCR 作为参考,当分析 Ct 值在质谱仪检测限内(Ct≤30)的无症状个体采集的临床样本时,我们证明基于 LC-MS 的方法具有 100%的负百分比一致性(估计特异性)和 95%的正百分比一致性(估计灵敏度)。这些结果表明,基于 LC-MS 的可扩展分析方法在未来的大流行准备中心具有一席之地,可以补充当前的病毒检测技术。