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Insights from the predicted interactions of plant derived compounds to the gluco-corticoid receptor as an alternative to dexa-methasone

机译:从植物衍生化合物与糖皮质激素受体(作为地塞米松的替代品)相互作用的预测相互作用中获得的见解

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摘要

Dexamethasone (DEX) an anti-inflamatory 9-fluoro-glucocorticoid, activates the cytosolic glucocorticoid receptor (GR) binding to its Ligand Binding Domain (LBD). The GR-ligand complex then translocates to the nucleus and binds to the Glucocorticoid Response Element (GRE) resulting up-regulation of target gene expression of anti-inflamatory proteins. DEX is one of the most effective ligand for GR activation but comply to side effects. Therefore, alternative for DEX – plant metabolites of Calotropis sp and Swertia chirata were screened using docking appraoch. These plants compounds were selected because; parts of these plants are widely used againsts inflamation, allergy, asthma etc. Three metabolites of Swertia chirata namely Gentianine (GENT), Xanthone (XANT) and Swerchirin (SWER) are found to be occupying the same binding pocket in the LBD of the GR (PDB ID 1M2Z). The binding affinity as reflected by binding energies of GENT-1M2Z, XANT-1M2Z and SWER-1M2Z are -5.6, -6.7 and -6.7, and all the output parameter of the respective compounds positively correlates with that of DEX-1M2Z with r = 0.9, 0.6 and 0.6 respectively indicating similar GR activation function. Visualization analysis of the models clearly indicates that GENT and SWER may be GR activators. Rest of the compounds mostly docked onto the surface of the receptor molecule.
机译:地塞米松(DEX)是一种抗炎性9-氟-糖皮质激素,可激活与其糖配体结合域(LBD)结合的胞浆糖皮质激素受体(GR)。然后,GR-配体复合物易位至细胞核并与糖皮质激素反应元件(GRE)结合,从而导致抗炎蛋白的靶基因表达上调。 DEX是GR活化最有效的配体之一,但具有副作用。因此,使用对接方法筛选了DEX – Calotropis sp和Swertia chirata的植物代谢物。选择这些植物化合物是因为;这些植物的一部分被广泛用于抵抗发炎,过敏,哮喘等。发现金边碱(GENT),黄酮(XANT)和Swerchirin(SWER)的三种Swertia chirata代谢物在GR的LBD中占据相同的结合口袋。 (PDB ID 1M2Z)。由GENT-1M2Z,XANT-1M2Z和SWER-1M2Z的结合能反映的结合亲和力为-5.6,-6.7和-6.7,且各化合物的所有输出参数与DEX-1M2Z的输出参数正相关,其中r = 0.9、0.6和0.6分别表示相似的GR激活功能。模型的可视化分析清楚地表明,GENT和SWER可能是GR激活剂。其余化合物大部分停靠在受体分子的表面上。

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