Screening of small molecule inhibitors against RhoA protein from Alisma using an online detection system

被引:0
|
作者
Yan, Chenjia [1 ]
Wang, Hong [1 ]
Chen, Shizhong [1 ]
机构
[1] Peking Univ, Sch Pharmaceut Sci, Dept Nat Med, 38 Xueyuan Rd, Beijing 100191, Peoples R China
基金
中国国家自然科学基金;
关键词
RhoA protein; Small molecule inhibitor; Alisma; Online activity screening system; SPR; BINDING; GTPASES; DNA;
D O I
10.1016/j.chroma.2022.463558
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Targeted high-throughput screening of inhibitors from natural products is an effective approach in the treatment of cancer progression. RhoA protein is essential for many signaling pathways. It is closely re-lated to the occurrence and development of tumor. So far, there are only a few reports on the screen-ing of small molecule inhibitors of RhoA protein from natural products. In this study, an online UHPLC-PDA-MS2-RhoA-FLD screening system was established for the first time to identify RhoA inhibitors from medicinal Alisma. Using this online system by adding fluorescent probes protopine [LZ1] to proteins, 17 active components were identified from Alisma, including 14 terpenoids. Their binding abilities were eval-uated by Surface Plasmon Resonance experiments. The activities of representative compounds were tested and showed anti-proliferative effect in cancer cells. Mechanistic studies showed that these compounds were able to downregulate the cellular expressions of RhoA associated proteins. This study provides po-tential lead compounds as small molecule inhibitors of RhoA protein for cancer therapy. This reported method can be used for targeted screening of small molecule inhibitors against tumors, and provides an approach for screening tumor inhibitors from natural products.(c) 2022 Elsevier B.V. All rights reserved.
引用
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页数:10
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