Your browser doesn't support javascript.
loading
Identifying citrus limonoids as a potential fusion inhibitor of DENV-2 virus through its in silico study and FTIR analysis.
Das, Satyajit; Sarma, Geetartha; Panicker, Nithin J; Sahu, Partha P.
Affiliation
  • Das S; Department of Electronics and Telecommunication Engineering, Jorhat Institute of Science and Technology, Jorhat, Assam 785010 India.
  • Sarma G; Department of Electronics and Communication Engineering, Tezpur University, Tezpur, Assam 784028 India.
  • Panicker NJ; Department of Electronics and Communication Engineering, Tezpur University, Tezpur, Assam 784028 India.
  • Sahu PP; Department of Electronics and Communication Engineering, Tezpur University, Tezpur, Assam 784028 India.
In Silico Pharmacol ; 12(1): 35, 2024.
Article in En | MEDLINE | ID: mdl-38680655
ABSTRACT
Dengue virus type 2 (DENV-2) is an arthropod-borne deadly RNA human pathogen transmitted through the mosquito Aedes. The DENV-2 roots viral infection by facilitating entry with its envelope glycoprotein to the receptor protein Dendritic-cell-specific ICAM3-grabbing non-integrin (DC-SIGN) through membrane fusion. Here, an organizational path is reported for inhibiting the transition due to fusion activation and by blocking the residues of the DC-SIGN-E-Glyco protein complex through citrus limonoids with its antiviral effect. Based on lower binding affinity obtained with E-glycoprotein, and based on ADMET and drug-likeness study, limonin was selected as having effective interaction with DC-SIGN-E-glycoprotein complex in comparison to other citrus limonoids. The FTIR spectra performed with the limonin-E-glycoprotein sample provide evidence of hydrogen bond formation that indicates the formation of a strong limonin-E-glycoprotein conjugate. Further, the strong physical interaction between DC-SIGN and small limonin molecules in comparison to that of E-glyco with DC-SIGN assures the development of immunity against DENV-2. Supplementary Information The online version contains supplementary material available at 10.1007/s40203-024-00207-2.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: In Silico Pharmacol Year: 2024 Document type: Article Country of publication: Germany

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: In Silico Pharmacol Year: 2024 Document type: Article Country of publication: Germany