Suppr超能文献

巨噬细胞移动抑制因子可作为一种新合成化合物 1-(9'-甲基-3'-咔唑)-3,4-二氢-β-咔啉的潜在作用靶点。

Macrophage Migration Inhibitory Factor Acts as the Potential Target of a Newly Synthesized Compound, 1-(9'-methyl-3'-carbazole)-3, 4-dihydro-β-carboline.

机构信息

Graduate Institute of Physiology, College of Medicine, National Taiwan University, Taipei, Taiwan.

School of Pharmacy, College of Medicine, National Taiwan University, Taipei, Taiwan.

出版信息

Sci Rep. 2019 Feb 14;9(1):2147. doi: 10.1038/s41598-019-38590-y.

Abstract

For a newly synthesized compound, identifying its target protein is a slow but pivotal step toward understand its pharmacologic mechanism. In this study, we systemically synthesized novel manzamine derivatives and chose 1-(9'-methyl-3'-carbazole)-3, 4-dihydro-β-carboline (MCDC) as an example to identify its target protein and function. MCDC had potent toxicity against several cancer cells. To identify its target protein, we first used a docking screen to predict macrophage migration inhibitory factor (MIF) as the potential target. Biochemical experiments, including mutation analysis and hydrogen-deuterium exchange assays, validated the binding of MCDC to MIF. Furthermore, MCDC was shown by microarrays to interfere with the cell cycle of breast cancer MCF7 cells. The activated signaling pathways included AKT phosphorylation and S phase-related proteins. Our results showed MIF as a potential direct target of a newly synthesized manzamine derivative, MCDC, and its pharmacologic mechanisms.

摘要

对于新合成的化合物,确定其靶蛋白是理解其药理机制的一个缓慢但关键的步骤。在这项研究中,我们系统地合成了新型曼扎宁衍生物,并选择 1-(9'-甲基-3'-咔唑)-3,4-二氢-β-咔啉(MCDC)作为一个例子来鉴定其靶蛋白和功能。MCDC 对几种癌细胞具有很强的毒性。为了鉴定其靶蛋白,我们首先使用对接筛选预测巨噬细胞移动抑制因子(MIF)作为潜在的靶标。生化实验,包括突变分析和氢氘交换实验,验证了 MCDC 与 MIF 的结合。此外,微阵列显示 MCDC 干扰乳腺癌 MCF7 细胞的细胞周期。激活的信号通路包括 AKT 磷酸化和 S 期相关蛋白。我们的结果表明 MIF 是新合成的曼扎宁衍生物 MCDC 的一个潜在的直接靶标,以及其药理机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97a7/6375994/4ac235a9483d/41598_2019_38590_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验