Identification of Potent Natural Resource Small Molecule Inhibitor to Control Vibrio cholera by Targeting Its Outer Membrane Protein U: An In Silico Approach.
Abdul RahamanAbdulraheem Ali AlmalkiMisbahuddin M RafeeqOmar AkhtarFarah AnjumMutaib Mosaued MashraqiZiaullah M SainAhmad AlzamamiVarish AhmadXin-An ZengQazi Mohammad Sajid JamalPublished in: Molecules (Basel, Switzerland) (2021)
Vibrio cholerae causes the diarrheal disease cholera which affects millions of people globally. The outer membrane protein U (OmpU) is the outer membrane protein that is most prevalent in V. cholerae and has already been recognized as a critical component of pathogenicity involved in host cell contact and as being necessary for the survival of pathogenic V. cholerae in the host body. Computational approaches were used in this study to screen a total of 37,709 natural compounds from the traditional Chinese medicine (TCM) database against the active site of OmpU. Following a sequential screening of the TCM database, we report three lead compounds-ZINC06494587, ZINC85510056, and ZINC95910434-that bind strongly to OmpU, with binding affinity values of -8.92, -8.12, and -8.78 kcal/mol, which were higher than the control ligand (-7.0 kcal/mol). To optimize the interaction, several 100 ns molecular dynamics simulations were performed, and the resulting complexes were shown to be stable in their vicinity. Additionally, these compounds were predicted to have good drug-like properties based on physicochemical properties and ADMET assessments. This study suggests that further research be conducted on these compounds to determine their potential use as cholera disease treatment.
Keyphrases
- molecular dynamics simulations
- small molecule
- molecular docking
- adverse drug
- oxide nanoparticles
- high throughput
- single cell
- protein protein
- cell therapy
- cystic fibrosis
- mass spectrometry
- mesenchymal stem cells
- electronic health record
- candida albicans
- human health
- pseudomonas aeruginosa
- dengue virus
- drug induced
- dna binding
- anti inflammatory
- replacement therapy
- bioinformatics analysis