Identifying the drug-target interactome of small molecule therapeutics is essential for understanding the full pharmacological effects of a compound. These therapies often induce changes within the cellular proteome, leading to unexpected consequences such as changes in the targets complexation state or off-target interactions between the compound and additional proteins. Currently, unbiased target-ID approaches are being used to embark on this task. Here we provide an overview of the strengths and limitations of these methods, and a practical step-by-step protocol for using the BioTAC system to assist with drug target and interactome ID.
Measuring Ligand-bound Protein Complexes with Proximity Labeling: A Practical Guide.
利用邻近标记法测量配体结合蛋白复合物:实用指南
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作者:Goyal Pavitra, Tao Andrew J, Mumby Elizabeth J, English Justin G, Ferguson Fleur M
| 期刊: | Chembiochem | 影响因子: | 2.800 |
| 时间: | 2024 | 起止号: | 2024 May 17; 25(10):e202400073 |
| doi: | 10.1002/cbic.202400073 | 研究方向: | 其它 |
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