Department of Molecular Biosciences, Department of Chemistry, and the Feinberg School of Medicine, Northwestern University, Evanston, IL, USA.
National High Magnetic Field Laboratory, Florida State University, Tallahassee, FL, USA.
Science. 2022 Jan 28;375(6579):411-418. doi: 10.1126/science.aaz5284. Epub 2022 Jan 27.
Human biology is tightly linked to proteins, yet most measurements do not precisely determine alternatively spliced sequences or posttranslational modifications. Here, we present the primary structures of ~30,000 unique proteoforms, nearly 10 times more than in previous studies, expressed from 1690 human genes across 21 cell types and plasma from human blood and bone marrow. The results, compiled in the Blood Proteoform Atlas (BPA), indicate that proteoforms better describe protein-level biology and are more specific indicators of differentiation than their corresponding proteins, which are more broadly expressed across cell types. We demonstrate the potential for clinical application, by interrogating the BPA in the context of liver transplantation and identifying cell and proteoform signatures that distinguish normal graft function from acute rejection and other causes of graft dysfunction.
人类生物学与蛋白质紧密相关,但大多数测量方法并不能精确地确定选择性剪接序列或翻译后修饰。在这里,我们展示了来自 1690 个人类基因在 21 种细胞类型以及来自人类血液和骨髓的血浆中的约 30000 种独特蛋白异构体的一级结构,这几乎是之前研究的 10 倍。研究结果汇编在血液蛋白异构体图谱(BPA)中,表明蛋白异构体可以更好地描述蛋白质水平的生物学,并且比它们对应的蛋白更能特异性地指示分化,因为蛋白在细胞类型中更广泛地表达。我们通过在肝移植的背景下研究 BPA 并确定区分正常移植物功能与急性排斥反应和其他移植物功能障碍原因的细胞和蛋白异构体特征,证明了其在临床应用中的潜力。