NCE CECR Prevention of Organ Failure (PROOF) Centre of Excellence, Vancouver, British Columbia, Canada.
PLoS Comput Biol. 2013 Apr;9(4):e1002963. doi: 10.1371/journal.pcbi.1002963. Epub 2013 Apr 4.
Recent technical advances in the field of quantitative proteomics have stimulated a large number of biomarker discovery studies of various diseases, providing avenues for new treatments and diagnostics. However, inherent challenges have limited the successful translation of candidate biomarkers into clinical use, thus highlighting the need for a robust analytical methodology to transition from biomarker discovery to clinical implementation. We have developed an end-to-end computational proteomic pipeline for biomarkers studies. At the discovery stage, the pipeline emphasizes different aspects of experimental design, appropriate statistical methodologies, and quality assessment of results. At the validation stage, the pipeline focuses on the migration of the results to a platform appropriate for external validation, and the development of a classifier score based on corroborated protein biomarkers. At the last stage towards clinical implementation, the main aims are to develop and validate an assay suitable for clinical deployment, and to calibrate the biomarker classifier using the developed assay. The proposed pipeline was applied to a biomarker study in cardiac transplantation aimed at developing a minimally invasive clinical test to monitor acute rejection. Starting with an untargeted screening of the human plasma proteome, five candidate biomarker proteins were identified. Rejection-regulated proteins reflect cellular and humoral immune responses, acute phase inflammatory pathways, and lipid metabolism biological processes. A multiplex multiple reaction monitoring mass-spectrometry (MRM-MS) assay was developed for the five candidate biomarkers and validated by enzyme-linked immune-sorbent (ELISA) and immunonephelometric assays (INA). A classifier score based on corroborated proteins demonstrated that the developed MRM-MS assay provides an appropriate methodology for an external validation, which is still in progress. Plasma proteomic biomarkers of acute cardiac rejection may offer a relevant post-transplant monitoring tool to effectively guide clinical care. The proposed computational pipeline is highly applicable to a wide range of biomarker proteomic studies.
近年来,定量蛋白质组学领域的技术进步刺激了大量各种疾病的生物标志物发现研究,为新的治疗方法和诊断方法提供了途径。然而,固有挑战限制了候选生物标志物成功转化为临床应用,因此需要一种稳健的分析方法学从生物标志物发现过渡到临床实施。我们已经开发了一种用于生物标志物研究的端到端计算蛋白质组学管道。在发现阶段,该管道强调实验设计、适当的统计方法和结果质量评估的不同方面。在验证阶段,该管道侧重于将结果迁移到适合外部验证的平台,并基于经过验证的蛋白质生物标志物开发分类器评分。在最后一个向临床实施的阶段,主要目标是开发和验证适合临床部署的测定法,并使用开发的测定法校准生物标志物分类器。该提出的管道应用于心脏移植的生物标志物研究,旨在开发一种微创临床测试来监测急性排斥反应。从对人血浆蛋白质组的非靶向筛选开始,鉴定了五个候选生物标志物蛋白。排斥反应调节蛋白反映了细胞和体液免疫反应、急性期炎症途径和脂质代谢生物过程。针对五个候选生物标志物开发了多重多重反应监测质谱 (MRM-MS) 测定法,并通过酶联免疫吸附 (ELISA) 和免疫比浊测定法 (INA) 进行了验证。基于经过验证的蛋白质的分类器评分表明,开发的 MRM-MS 测定法为外部验证提供了一种合适的方法,该验证仍在进行中。急性心脏排斥的血浆蛋白质组生物标志物可能为有效的临床护理提供一种相关的移植后监测工具。所提出的计算管道非常适用于广泛的生物标志物蛋白质组学研究。