1. Academic Validation
  2. Phytochemical constituents of Inula britannica as potential inhibitors of dihydrofolate reductase: A strategic approach against shigellosis

Phytochemical constituents of Inula britannica as potential inhibitors of dihydrofolate reductase: A strategic approach against shigellosis

  • J Biomol Struct Dyn. 2022;40(22):11932-11947. doi: 10.1080/07391102.2021.1966508.
Sandra Jose 1 Sreevidya S Devi 2 Shakthi P 3 Khattab Al-Khafaji 4
Affiliations

Affiliations

  • 1 Department of Biotechnology, Vels Institute of Science, Technology and Advanced Studies, Chennai, Tamil Nadu, India.
  • 2 School of Biosciences, Mar Athanasios College for Advanced Studies, Thiruvalla, Kerala, India.
  • 3 Department of Biotechnology, Sri Krishna Arts and Science College, Coimbatore, Tamil Nadu, India.
  • 4 Faculty of Arts and Sciences, Department of Chemistry, Gaziantep University, Gaziantep, Turkey.
Abstract

Shigella dysenteriae type 1 is considered as an epidemic in different developing countries, which is responsible for the most severe form of Bacterial dysentery. It habitually can develop to the most severe form of dysentery with deadly complications. Development of drugs against this disease is still ongoing. Therefore, we used in silico studies to screen the Inula britannica phytocompounds that are used in traditional Chinese and Kampo Medicines and have activities against different diseases. Spinacetin, eupatin, chrysoeriol and diosmetin were successfully passed through the docking-based screening and absorption, distribution, metabolism, excretion and toxicity (ADMET) filtration. The estimated docking affinities of eupatin, diosmetin, chrysoeriol and spinacetin with Dihydrofolate reductase type 1 (DHFR-1), were -6.5, -6.5, -6.3 and -6.1 kcal/mol, respectively. Which were selected for further investigations based on their favorable ADME/Tox characteristics. Then, the 100 ns molecular dynamics (MD) simulations of apo DHFR, spinacetin-DHFR, eupatin-DHFR, chrysoeriol-DHFR and diosmetin-DHFR complexes were carried out. The RMSD fluctuations of the spinacetin, eupatin, chrysoeriol and diosmetin inside the binding site were explored. Subsequently, the effect of binding Spinacetin, eupatin, chrysoeriol and diosmetin upon the dynamic stability of protein was assessed. Additionally, Principal Component Analysis (PCA) and Hydrogen bond analysis was performed for the apo protein and the protein ligand complexes. The results revealed that chrysoeriol and eupatin has good inhibitory effects against DHFR-1 as treatment for Shigella dysenteriae type when compared to other compounds under study. Hence this study implies that eupatin and chrysoeriol are a significantly potential drug like molecule for the treatment of Shigellosis and must undergo validation through in vivo and in vitro experiments.Communicated by Ramaswamy H. Sarma.

Keywords

DHFR type 1; In-silico screening; Inula Britannica; Shigella dysenteriae type 1; Shigellosis.

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