通过细胞热转移检测法定量检测人体全血中 RIPK1 的目标参与情况,以实现潜在的临床前和临床应用

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-03-01 DOI:10.1016/j.slasd.2023.12.007
Shitalben Patel , Marie Karlsson , Joseph T. Klahn , Frank Gambino Jr. , Helena Costa , Kathleen A. McGuire , Christina K. Baumgartner , Jon Williams , Sarah Sandoz , James E. Kath
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引用次数: 0

摘要

细胞热转移分析法 (CETSA®) 是一种广泛用于小分子化合物临床前表征的目标参与方法。CETSA® 已用于分离 PBMC 的全血半定量读数,以及使用细胞系的平板定量读数。然而,CETSA® 还没有在未经处理的人体全血中进行定量评估,而临床应用更倾向于使用这种方法。在此,我们报告了两种不同的检测方法--Alpha CETSA® 和 MSD CETSA®,每份样本只需不到 100 μL 的全血,无需分离 PBMC。我们选择 RIPK1 作为概念验证靶点,并通过测量七种不同抑制剂的参与情况,证明了检测的高灵敏度和稳健性。这些定量 CETSA® 平台可应用于临床前药代动力学-药效学研究,并在临床试验中直接与小分子靶标结合。
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Quantitative target engagement of RIPK1 in human whole blood via the cellular thermal shift assay for potential pre-clinical and clinical applications

The cellular thermal shift assay (CETSA®) is a target engagement method widely used for preclinical characterization of small molecule compounds. CETSA® has been used for semi-quantitative readouts in whole blood with PBMC isolation, and quantitative, plate-based readouts using cell lines. However, there has been no quantitative evaluation of CETSA® in unprocessed human whole blood, which is preferred for clinical applications. Here we report two separate assay formats – Alpha CETSA® and MSD CETSA® – that require less than 100 μL of whole blood per sample without PBMC isolation. We chose RIPK1 as a proof-of-concept target and, by measuring engagement of seven different inhibitors, demonstrate high assay sensitivity and robustness. These quantitative CETSA® platforms enable possible applications in preclinical pharmacokinetic-pharmacodynamic studies, and direct target engagement with small molecules in clinical trials.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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