Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA.
Nat Biotechnol. 2011 Jun 19;29(7):635-43. doi: 10.1038/nbt.1899.
We developed a pipeline to integrate the proteomic technologies used from the discovery to the verification stages of plasma biomarker identification and applied it to identify early biomarkers of cardiac injury from the blood of patients undergoing a therapeutic, planned myocardial infarction (PMI) for treatment of hypertrophic cardiomyopathy. Sampling of blood directly from patient hearts before, during and after controlled myocardial injury ensured enrichment for candidate biomarkers and allowed patients to serve as their own biological controls. LC-MS/MS analyses detected 121 highly differentially expressed proteins, including previously credentialed markers of cardiovascular disease and >100 novel candidate biomarkers for myocardial infarction (MI). Accurate inclusion mass screening (AIMS) qualified a subset of the candidates based on highly specific, targeted detection in peripheral plasma, including some markers unlikely to have been identified without this step. Analyses of peripheral plasma from controls and patients with PMI or spontaneous MI by quantitative multiple reaction monitoring mass spectrometry or immunoassays suggest that the candidate biomarkers may be specific to MI. This study demonstrates that modern proteomic technologies, when coherently integrated, can yield novel cardiovascular biomarkers meriting further evaluation in large, heterogeneous cohorts.
我们开发了一个从发现到验证阶段整合蛋白质组学技术的管道,应用该管道来鉴定接受计划心肌梗死(PMI)治疗肥厚型心肌病患者血液中的早期心脏损伤生物标志物。在受控心肌损伤前后直接从患者心脏中采样,确保候选生物标志物的富集,并允许患者作为自身的生物学对照。LC-MS/MS 分析检测到 121 种高度差异表达的蛋白质,包括先前有心血管疾病标志物资格的标志物和 >100 种新的心肌梗死(MI)候选生物标志物。基于在周围血浆中的高度特异性、靶向检测,准确纳入质量筛选(AIMS)合格的候选者子集,包括如果没有这一步骤可能不会被识别的一些标志物。通过定量多重反应监测质谱或免疫测定法对接受 PMI 或自发性 MI 治疗的患者和对照者的外周血浆进行分析,表明候选生物标志物可能是 MI 特异性的。这项研究表明,当蛋白质组学技术一致整合时,可以产生新的心血管生物标志物,值得在大型、异质队列中进一步评估。