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从生物活性植物成分中鉴定钙/钙调蛋白依赖性蛋白激酶 IV 的潜在抑制剂。

Identification of Potential Inhibitors of Calcium/Calmodulin-Dependent Protein Kinase IV from Bioactive Phytoconstituents.

机构信息

Centre for Interdisciplinary Research in Basic Sciences, Jamia Millia Islamia, Jamia Nagar, New Delhi 110025, India.

Department of Clinical Microbiology and Infectious Diseases, School of Pathology, University of the Witwatersrand, Johannesburg 2193, South Africa.

出版信息

Oxid Med Cell Longev. 2020 Jul 16;2020:2094635. doi: 10.1155/2020/2094635. eCollection 2020.

Abstract

Calcium/calmodulin-dependent protein kinase IV (CaMKIV) is an upstream regulator of CaMKK-CaMKIV signaling cascade that activates various transcription factors, thereby regulating several cellular activities including, neuronal communication and immune response. Owing to the abnormal expression in cancer and neurodegenerative diseases, the CaMKIV has been considered a potential drug target. In the present study, we checked the binding affinity of plant-derived natural compounds viz., quercetin, ellagic acid (EA), simvastatin, capsaicin, ursolic acid, DL--tocopherol acetate, and limonin towards CaMKIV. Molecular docking and fluorescence binding studies showed that EA and quercetin bind to the CaMKIV with a considerable affinity in comparison to other compounds. Enzyme inhibition assay revealed that both EA and quercetin inhibit CaMKIV activity with their IC values in the micromolar range. To get atomistic insights into the mode of interactions, inhibition mechanism, and the stability of the CaMKIV-ligand complex, a 100 ns MD simulation analysis was performed. Both EA and quercetin bind to the catalytically important residues of active site pocket of CaMKIV forming enough stabilizing interactions presumably inhibiting enzyme activity. Moreover, no significant structural change in the CaMKIV was observed upon binding of EA and quercetin. In conclusion, this study illustrates the application of phytoconstituents in the development of therapeutic molecules targeting CaMKIV having implications in cancer and neurodegenerative diseases after validation.

摘要

钙/钙调蛋白依赖性蛋白激酶 IV(CaMKIV)是 CaMKK-CaMKIV 信号级联的上游调节剂,可激活各种转录因子,从而调节包括神经元通讯和免疫反应在内的多种细胞活动。由于在癌症和神经退行性疾病中的异常表达,CaMKIV 被认为是一个潜在的药物靶点。在本研究中,我们检查了植物源性天然化合物,如槲皮素、鞣花酸(EA)、辛伐他汀、辣椒素、熊果酸、DL--生育酚乙酸酯和柠檬苦素与 CaMKIV 的结合亲和力。分子对接和荧光结合研究表明,与其他化合物相比,EA 和槲皮素与 CaMKIV 具有相当大的亲和力。酶抑制试验表明,EA 和槲皮素均以微摩尔级别的 IC 值抑制 CaMKIV 活性。为了深入了解相互作用模式、抑制机制以及 CaMKIV-配体复合物的稳定性,进行了 100ns 的 MD 模拟分析。EA 和槲皮素均与 CaMKIV 活性位点口袋的催化重要残基结合,形成足够的稳定相互作用,可能抑制酶活性。此外,在 EA 和槲皮素结合后,未观察到 CaMKIV 结构发生明显变化。总之,这项研究说明了植物成分在开发针对 CaMKIV 的治疗分子中的应用,这对癌症和神经退行性疾病具有潜在的影响,需要进一步验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c651/7382742/b43ef779e321/OMCL2020-2094635.001.jpg

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