Department of Chemistry, University of Wisconsin-Madison, Madison, Wisconsin 53706, United States.
Department of Surgery, University of Wisconsin-Madison, Madison, Wisconsin 53705, United States.
J Am Soc Mass Spectrom. 2021 Jun 2;32(6):1278-1294. doi: 10.1021/jasms.1c00099. Epub 2021 May 13.
Top-down mass spectrometry (MS)-based proteomics is a powerful technology for comprehensively characterizing proteoforms to decipher post-translational modifications (PTMs) together with genetic variations and alternative splicing isoforms toward a proteome-wide understanding of protein functions. In the past decade, top-down proteomics has experienced rapid growth benefiting from groundbreaking technological advances, which have begun to reveal the potential of top-down proteomics for understanding basic biological functions, unraveling disease mechanisms, and discovering new biomarkers. However, many challenges remain to be comprehensively addressed. In this Account & Perspective, we discuss the major challenges currently facing the top-down proteomics field, particularly in protein solubility, proteome dynamic range, proteome complexity, data analysis, proteoform-function relationship, and analytical throughput for precision medicine. We specifically review the major technology developments addressing these challenges with an emphasis on our research group's efforts, including the development of top-down MS-compatible surfactants for protein solubilization, functionalized nanoparticles for the enrichment of low-abundance proteoforms, strategies for multidimensional chromatography separation of proteins, and a new comprehensive user-friendly software package for top-down proteomics. We have also made efforts to connect proteoforms with biological functions and provide our visions on what the future holds for top-down proteomics.
自上而下的质谱(MS)基蛋白质组学是一种强大的技术,可全面表征蛋白质形式,以破译翻译后修饰(PTMs)以及遗传变异和选择性剪接异构体,从而全面了解蛋白质的功能。在过去的十年中,自上而下的蛋白质组学受益于开创性的技术进步,经历了快速发展,这些进步开始揭示自上而下的蛋白质组学在理解基本生物学功能、揭示疾病机制和发现新的生物标志物方面的潜力。然而,仍有许多挑战需要全面解决。在本观点和观点中,我们讨论了自上而下的蛋白质组学领域当前面临的主要挑战,特别是在蛋白质溶解度、蛋白质组动态范围、蛋白质组复杂性、数据分析、蛋白质形式-功能关系以及精准医学的分析通量方面。我们特别回顾了针对这些挑战的主要技术发展,重点介绍了我们研究小组的努力,包括开发与自上而下的 MS 兼容的用于蛋白质溶解的表面活性剂、用于富集低丰度蛋白质形式的功能化纳米粒子、用于蛋白质多维色谱分离的策略,以及用于自上而下的蛋白质组学的新的全面用户友好的软件包。我们还努力将蛋白质形式与生物学功能联系起来,并对自上而下的蛋白质组学的未来发展提出我们的看法。