Chan Zuckerberg Biohub, Stanford, California 94305, United States.
Otolaryngology Head and Neck Surgery Research Division, Stanford University, Stanford, California 94305, United States.
J Proteome Res. 2021 Jan 1;20(1):393-408. doi: 10.1021/acs.jproteome.0c00464. Epub 2020 Dec 17.
Major histocompatibility complex (MHC)-presented peptides (pMHC) give insight into T cell immune responses, a critical step toward developing a new generation of targeted immunotherapies. Recent instrumentation advances have propelled mass spectrometry to being arguably the most robust technology for discovering and quantifying naturally presented pMHC from cells and tissues. However, sample preparation has remained a major limitation due to time-consuming and labor-intensive workflows. We developed a high-throughput and automated platform with enhanced speed, sensitivity, and reproducibility relative to prior studies. This pipeline is capable of processing up to 96 samples in 6 h or less yielding high-quality pMHC mixtures ready for mass spectrometry. Here, we describe our efforts to optimize purification and mass spectrometer parameters, ultimately allowing us to identify as many as almost 5000 pMHC I and 7400 pMHC II from as little as 2.5 × 10 Raji cells each. We believe that this platform will facilitate and accelerate immunopeptidome profiling and benefit clinical research for immunotherapies.
主要组织相容性复合体 (MHC) 呈递的肽段 (pMHC) 为 T 细胞免疫反应提供了深入了解,这是开发新一代靶向免疫疗法的关键步骤。最近的仪器仪表进步推动了质谱技术的发展,使其成为从细胞和组织中发现和定量天然呈递的 pMHC 的最强大技术之一。然而,由于工作流程耗时且劳动强度大,样品制备仍然是一个主要限制。我们开发了一种高通量和自动化的平台,与之前的研究相比,该平台具有增强的速度、灵敏度和重现性。该流水线能够在 6 小时或更短的时间内处理多达 96 个样本,产生高质量的 pMHC 混合物,可直接用于质谱分析。在这里,我们描述了优化纯化和质谱仪参数的努力,最终使我们能够从每个 2.5×10 Raji 细胞中鉴定多达近 5000 个 MHC I 和 7400 个 MHC II pMHC。我们相信,该平台将促进和加速免疫肽组学分析,并有益于免疫疗法的临床研究。