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采用完整蛋白 MS 和靶向 MRM 技术对 KRAS 不可逆共价抑制剂进行高通量动力学表征。

High-Throughput Kinetic Characterization of Irreversible Covalent Inhibitors of KRAS by Intact Protein MS and Targeted MRM.

机构信息

Biochemical and Cellular Pharmacology, Genentech, Inc., South San Francisco, California 94080, United States.

Confluence, 4340 Duncan Avenue, Suite 400, St. Louis, Missouri 63110, United States.

出版信息

Anal Chem. 2022 Jan 18;94(2):1230-1239. doi: 10.1021/acs.analchem.1c04463. Epub 2022 Jan 6.

Abstract

With recent advances and success in several drugs designed to treat acute and chronic diseases, targeted covalent inhibitors show a resurgence in drug discovery. As covalent inhibition is time-dependent, the preferred quantitative potency metric of irreversible inhibitors is the second-order rate constant /, rather than IC. Here, we present the development of a mass spectrometry-based platform for rapid kinetic analysis of irreversible covalent inhibitors. Using a simple liquid handling robot for automated sample preparation and a solid-phase extraction-based RapidFire-MS system for rapid MS analysis, kinetic characterization of covalent inhibitors was performed in high throughput both by intact protein analysis and targeted multiple reaction monitoring (MRM). In addition, a bimolecular reaction model was applied to extract / in data fitting, providing tremendous flexibility in the experimental design to characterize covalent inhibitors with various properties. Using KRAS inhibitors as a test case, the platform was demonstrated to be effective for studying covalent inhibitors with a wide range of / values from single digit to 3 × 10 M s.

摘要

随着针对急性和慢性疾病的几种药物的最新进展和成功,靶向共价抑制剂在药物发现中重新兴起。由于共价抑制是时间依赖性的,不可逆抑制剂的首选定量效力度量标准是二级速率常数 k,而不是 IC。在这里,我们提出了一种基于质谱的平台,用于快速动力学分析不可逆共价抑制剂。使用简单的液体处理机器人进行自动化样品制备和基于固相萃取的 RapidFire-MS 系统进行快速 MS 分析,通过完整蛋白分析和靶向多重反应监测(MRM)以高通量方式对共价抑制剂进行动力学表征。此外,双分子反应模型被应用于 k 提取进行数据拟合,为具有各种特性的共价抑制剂的表征提供了极大的实验设计灵活性。使用 KRAS 抑制剂作为测试案例,该平台被证明可有效地用于研究具有从单个数字到 3×10 M s 范围的各种 k 值的共价抑制剂。

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