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实时细胞热转移分析监测靶标结合。

Real-Time Cellular Thermal Shift Assay to Monitor Target Engagement.

机构信息

National Center for Advancing Translational Sciences, National Institutes of Health, Rockville, Maryland 20850, United States.

出版信息

ACS Chem Biol. 2022 Sep 16;17(9):2471-2482. doi: 10.1021/acschembio.2c00334. Epub 2022 Sep 1.

DOI:10.1021/acschembio.2c00334
PMID:36049119
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9486815/
Abstract

Determining a molecule's mechanism of action is paramount during chemical probe development and drug discovery. The cellular thermal shift assay (CETSA) is a valuable tool to confirm target engagement in cells for a small molecule that demonstrates a pharmacological effect. CETSA directly detects biophysical interactions between ligands and protein targets, which can alter a protein's unfolding and aggregation properties in response to thermal challenge. In traditional CETSA experiments, each temperature requires an individual sample, which restricts throughput and requires substantial optimization. To capture the full aggregation profile of a protein from a single sample, we developed a prototype real-time CETSA (RT-CETSA) platform by coupling a real-time PCR instrument with a CCD camera to detect luminescence. A thermally stable Nanoluciferase variant (ThermLuc) was bioengineered to withstand unfolding at temperatures greater than 90 °C and was compatible with monitoring target engagement events when fused to diverse targets. Utilizing well-characterized inhibitors of lactate dehydrogenase alpha, RT-CETSA showed significant correlation with enzymatic, biophysical, and other cell-based assays. A data analysis pipeline was developed to enhance the sensitivity of RT-CETSA to detect on-target binding. RT-CETSA technology advances capabilities of the CETSA method and facilitates the identification of ligand-target engagement in cells, a critical step in assessing the mechanism of action of a small molecule.

摘要

在化学探针开发和药物发现过程中,确定分子的作用机制至关重要。细胞热转移分析(CETSA)是一种用于确认具有药理作用的小分子在细胞中靶标结合的有效工具。CETSA 直接检测配体与蛋白靶标的生物物理相互作用,这些相互作用可以改变蛋白在热挑战下的展开和聚集特性。在传统的 CETSA 实验中,每个温度都需要一个单独的样本,这限制了通量,并且需要大量的优化。为了从单个样本中捕获蛋白的完整聚集谱,我们通过将实时 PCR 仪器与 CCD 相机耦合来检测发光,开发了一种实时 CETSA(RT-CETSA)原型平台。我们对热稳定的纳米荧光素酶变体(ThermLuc)进行了生物工程改造,使其能够在 90°C 以上的温度下展开,并与融合到不同靶标时监测靶标结合事件兼容。利用乳酸脱氢酶 alpha 的特征明确的抑制剂,RT-CETSA 显示出与酶学、生物物理和其他基于细胞的测定法的显著相关性。我们开发了一种数据分析管道来提高 RT-CETSA 检测靶标结合的灵敏度。RT-CETSA 技术提高了 CETSA 方法的能力,并促进了在细胞中鉴定配体-靶标结合,这是评估小分子作用机制的关键步骤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5790/9486815/6a400c44b4ac/cb2c00334_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5790/9486815/32bb939ea801/cb2c00334_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5790/9486815/05ec71e51411/cb2c00334_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5790/9486815/6ecb1e404ed9/cb2c00334_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5790/9486815/6a400c44b4ac/cb2c00334_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5790/9486815/32bb939ea801/cb2c00334_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5790/9486815/05ec71e51411/cb2c00334_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5790/9486815/6ecb1e404ed9/cb2c00334_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5790/9486815/6a400c44b4ac/cb2c00334_0005.jpg

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