Molecular docking studies of natural immunomodulators indicate their interactions with the CD40L of CD40/CD40L pathway and CSF1R kinase domain of microglia

被引:5
作者
Maurya, Shashank Kumar [1 ,2 ,3 ]
Mishra, Rajnikant [3 ]
机构
[1] Univ Delhi, Ramjas Coll, Dept Zool, Delhi 110007, India
[2] Cluster Univ Jammu, Sch Sci, Dept Zool, Jammu 180001, India
[3] Banaras Hindu Univ, Dept Zool, Biochem & Mol Biol Lab, Varanasi 221005, Uttar Pradesh, India
关键词
Microglia; Natural products; Protein-ligand interaction; Drug target; Molecular docking; MD simulation; LIGAND; BINDING; ROLES; INFLAMMATION; MECHANISM; DISCOVERY; NUMBER; SITES; TOOL;
D O I
10.1007/s00894-022-05084-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Natural products have proved beneficial in reducing neuroinflammation in neurological diseases. Their impacts have also been associated with the activities of microglia, responsible for brain-specific immunity. Recent studies have shown the involvement of the number of microglia-specific proteins in the regulation of brain-specific immunity. However, molecular targets of natural products and their mechanism of interaction with microglia-specific proteins are elusive. Since the genetic signature of microglia offers many potential targets for drug discovery, molecular docking followed by molecular dynamics (MD) simulations of cluster of differentiation 40 ligand (CD40L) and colony-stimulating factor 1 receptor (CSF1R) kinase domain protein with some known neuro-immunomodulators (Curcumin, Cannabidiol, Ginsenoside Rg1, Resveratrol, and Sulforaphane) has been evaluated. Curcumin and cannabidiol were observed likely to modulate CD40L and expression of cytokines and entry of inflammatory cells. Resveratrol and cannabidiol may affect the CSF1R kinase domain and activation of microglia. Our finding suggests that curcumin, cannabidiol, and resveratrol may serve specific drug ligands in regulating microglia-mediated brain immunity.
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页数:13
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