a Beijing Key Laboratory of Innovative Drug Discovery of Traditional Chinese Medicine (Natural Medicine) and Translational Medicine , Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College , Beijing , China.
b Key Laboratory of Bioactive Substances and Resources, Utilization of Chinese Herbal Medicine, Ministry of Education , Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College , Beijing , China.
Pharm Biol. 2019 Dec;57(1):133-139. doi: 10.1080/13880209.2018.1557699.
Calenduloside E (CE), one of the primary natural products found in Aralia elata (Miq.) Seem. (Araliaceae), possesses prominent anti-apoptotic potential. A previous study found that one of the anti-apoptotic CE targets is heat shock protein 90 AB1 (Hsp90AB1) by probe CE-P, while the other targets of CE still need to be identified with more efficient probes.
This study investigates CE analogue (CEA) as one clickable activity-based probe for use in exploring anti-apoptotic CE targets.
Pretreatment of HUVECs with CEA (1.25 μM) for 8 hr, followed by ox-LDL stimulation for 24 h. Flow cytometry analysis and JC-1 staining assays were performed The kinetic constant measurements were tested by the Biacore T200, CM5 Sensor Chip which was activated by using sulpho-NHS/EDC. Ligands were dissolved and injected with a concentration of 12.5, 6.25, 3.125, 1.56, 0.78 and 0 μM.
CEA was confirmed to possess an anti-apoptotic effect. The probable targets of CE/CEA were calculated, and as one of the higher scores proteins (Fit values: 0.88/0.86), Hsp90 properly got our attention. Molecular modelling study showed that both CE and CEA could bind to Hsp90 with the similar interaction, and the docking scores (S value) were -7.61 and -7.33. SPR assay provided more evidence to prove that CEA can interact with Hsp90 with the KD value 11.7 µM.
Our results suggest that clickable probe CEA could alleviate ox-LDL induced apoptosis by a similar mechanism of anti-apoptotic CE, and afforded the possibility of identifying additional anti-apoptotic targets of CE.
瓜叶菊皂苷 E(CE)是刺五加(Miq.)Seem.(五加科)中发现的主要天然产物之一,具有显著的抗细胞凋亡作用。先前的研究发现,抗凋亡 CE 的一个靶标是热休克蛋白 90 AB1(Hsp90AB1),探针 CE-P 就是以此为依据发现的,而 CE 的其他靶标仍需要用更有效的探针来确定。
本研究探讨 CE 类似物(CEA)作为一种点击活性探针,用于探索抗凋亡 CE 靶标。
将 HUVECs 用 CEA(1.25 μM)预处理 8 小时,然后用 ox-LDL 刺激 24 小时。采用流式细胞术分析和 JC-1 染色法进行检测。通过 Biacore T200 进行动力学常数测量,CM5 传感器芯片采用磺基-NHS/EDC 激活。配体溶解后以 12.5、6.25、3.125、1.56、0.78 和 0 μM 的浓度注入。
CEA 被证实具有抗凋亡作用。计算了 CE/CEA 的可能靶标,其中 HSP90 作为得分较高的蛋白之一(拟合值:0.88/0.86)引起了我们的注意。分子建模研究表明,CE 和 CEA 都可以与 HSP90 结合,具有相似的相互作用,对接评分(S 值)分别为-7.61 和-7.33。SPR 试验提供了更多证据证明 CEA 可以与 HSP90 以 KD 值 11.7 μM 相互作用。
我们的研究结果表明,点击探针 CEA 可以通过与抗凋亡 CE 类似的机制缓解 ox-LDL 诱导的细胞凋亡,并为鉴定 CE 的其他抗凋亡靶标提供了可能性。