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可点击的抗细胞凋亡活性探针——贯叶连翘苷 E。

The clickable activity-based probe of anti-apoptotic calenduloside E.

机构信息

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.

出版信息

Pharm Biol. 2019 Dec;57(1):133-139. doi: 10.1080/13880209.2018.1557699.

Abstract

CONTEXT

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.

OBJECTIVE

This study investigates CE analogue (CEA) as one clickable activity-based probe for use in exploring anti-apoptotic CE targets.

MATERIALS AND METHODS

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.

RESULTS

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.

DISCUSSION AND CONCLUSIONS

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.

摘要

背景

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。

目的

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。

材料和方法

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。

结果

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。

讨论与结论

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b523/6407588/764677aef850/IPHB_A_1557699_F0001_B.jpg

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