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热休克同源70千道尔顿蛋白是十四烷基2,3 - 二羟基苯甲酸在PC12细胞中产生促神经突生长作用的靶点。

Heat Shock Cognate 70 kDa Protein Is the Target of Tetradecyl 2,3-Dihydroxybenzoate for Neuritogenic Effect in PC12 Cells.

作者信息

Cheng Lihong, Wang Yanhui, Xiang Lan, Qi Jianhua

机构信息

College of Pharmaceutical Sciences, Zhejiang University, Hangzhou 310058, China.

出版信息

Biomedicines. 2021 Oct 16;9(10):1483. doi: 10.3390/biomedicines9101483.

Abstract

Tetradecyl 2,3-dihydroxybenzoate (ABG-001) is a lead compound derived from gentisides with a remarkable neuritogenic activity. However, the target of ABG-001 is yet to be defined to date. In this study, the potential target of ABG-001 was investigated via an activity-based protein profiling (ABPP) analysis, which is a chemical proteomic method for target identification by using chemical probes. Results indicated that the potential target proteins of ABG-001 were heat shock cognate 70 kDa protein (Hsc70), 78 kDa glucose-regulated protein (GRP78), and 14-3-3 theta protein. Then, the potential target of ABG-001 was confirmed by using inhibitors, the cellular thermal shift assay (CETSA) and small-interfering RNA (siRNA) analysis. The inhibitor of Hsc70 and siRNA significantly decreased the neurite outgrowth induced by ABG-001. Furthermore, ABG-001 induced neurite outgrowth was reduced by siRNA against Hsc70, and the results of CETSA suggested that Hsc70 showed a significant thermal stability-shifted effect upon ABG-001 treatment. These results indicated that Hsc70 is the target protein of ABG-001 in PC12 cells.

摘要

2,3 - 二羟基苯甲酸十四烷基酯(ABG - 001)是一种源自龙胆酸盐的先导化合物,具有显著的促神经突生长活性。然而,截至目前ABG - 001的靶点尚未明确。在本研究中,通过基于活性的蛋白质谱分析(ABPP)对ABG - 001的潜在靶点进行了研究,ABPP是一种利用化学探针进行靶点鉴定的化学蛋白质组学方法。结果表明,ABG - 001的潜在靶点蛋白为热休克同源70 kDa蛋白(Hsc70)、78 kDa葡萄糖调节蛋白(GRP78)和14 - 3 - 3θ蛋白。然后,通过使用抑制剂、细胞热位移分析(CETSA)和小干扰RNA(siRNA)分析对ABG - 001的潜在靶点进行了确认。Hsc70抑制剂和siRNA显著降低了ABG - 001诱导的神经突生长。此外,针对Hsc70的siRNA降低了ABG - 001诱导的神经突生长,CETSA结果表明,ABG - 001处理后Hsc70表现出显著的热稳定性变化效应。这些结果表明,Hsc70是ABG - 001在PC12细胞中的靶点蛋白。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7150/8533567/f4a1cef0de30/biomedicines-09-01483-g001.jpg

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