Department of Pharmaceutical Chemistry, University of California, San Francisco, San Francisco, CA, United States.
Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California San Diego, San Diego, CA, United States.
Methods Enzymol. 2023;682:375-411. doi: 10.1016/bs.mie.2022.09.009. Epub 2022 Dec 21.
Proteolysis is a central regulator of many biological pathways and the study of proteases has had a significant impact on our understanding of both native biology and disease. Proteases are key regulators of infectious disease and misregulated proteolysis in humans contributes to a variety of maladies, including cardiovascular disease, neurodegeneration, inflammatory diseases, and cancer. Central to understanding a protease's biological role, is characterizing its substrate specificity. This chapter will facilitate the characterization of individual proteases and complex, heterogeneous proteolytic mixtures and provide examples of the breadth of applications that leverage the characterization of misregulated proteolysis. Here we present the protocol of Multiplex Substrate Profiling by Mass Spectrometry (MSP-MS), a functional assay that quantitatively characterizes proteolysis using a synthetic library of physiochemically diverse, model peptide substrates, and mass spectrometry. We present a detailed protocol as well as examples of the use of MSP-MS for the study of disease states, for the development of diagnostic and prognostic tests, for the generation of tool compounds, and for the development of protease-targeted drugs.
蛋白水解是许多生物途径的重要调节因子,对蛋白酶的研究对我们对天然生物学和疾病的理解产生了重大影响。蛋白酶是传染病的关键调节剂,人类中失调的蛋白水解会导致多种疾病,包括心血管疾病、神经退行性疾病、炎症性疾病和癌症。要了解蛋白酶的生物学作用,关键是要描述其底物特异性。本章将有助于描述单个蛋白酶和复杂、异质的蛋白水解混合物,并提供利用失调蛋白水解进行描述的广泛应用的例子。在这里,我们提出了通过质谱(MS)进行多重底物谱分析(MSP-MS)的方案,这是一种使用物理化学性质多样的合成模型肽底物库和质谱定量描述蛋白水解的功能测定法。我们提供了详细的方案以及 MSP-MS 在疾病状态研究、诊断和预后测试开发、工具化合物生成以及蛋白酶靶向药物开发中的应用示例。