化学
离子液体
萃取(化学)
胶束
对接(动物)
生物物理学
色谱法
膜
分子动力学
组合化学
生物化学
计算化学
有机化学
医学
生物
护理部
催化作用
水溶液
作者
Hongwei Chu,Qun Zhao,Ju Liu,Kaiguang Yang,Yanlei Wang,Jianhui Liu,Kun Zhang,Baofeng Zhao,Hongyan He,Yong Zheng,Shijun Zhong,Zhen Liang,Lihua Zhang,Yukui Zhang
标识
DOI:10.1021/acs.analchem.1c03195
摘要
Limited by the rare efficient extraction system in extracting hydrophobic membrane protein complexes (MPCs) without compromising the stability of protein-protein interactions (PPIs), the in-depth functional study of MPCs has lagged far behind. In this study, the first systematic screening of ionic liquids (ILs) was performed and showed that triethylammonium acetate (TEAA) IL exhibited excellent performance in stabilizing PPIs, which was further confirmed by molecular docking simulations. By combining TEAA with the conventional detergent Nonidet P-40 (NP-40), a novel IL-based extraction system, i-TAN (TEAA IL with 1% NP-40), was proposed, which demonstrated superior performance in extracting and stabilizing MPCs, attributed to its larger size, more uniform distribution, and closer-to-neutral microenvironment of micelles. Extraction of MPCs with i-TAN allowed the confident identification of more hydrophobic EGFR-interacting proteins that are easily dissociated during the extraction process. Quantitative analysis of the difference in EGFR complexes between trastuzumab-sensitive and trastuzumab-resistant breast cancer cells provided comprehensive insights to understand the drug resistance mechanism, suggesting that i-TAN has great potential in interactomics and functional analysis of MPCs. This study provides a novel strategy for MPC extraction and downstream processing.
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