In-silico approach to investigate death domains associated with nano-particle-mediated cellular responses
| Autor: | Hussaina Banu, Mokashi Nida Nisar, Maria Christina Joseph |
|---|---|
| Rok vydání: | 2018 |
| Předmět: |
0301 basic medicine
Molecular model In silico Biochemistry 03 medical and health sciences Protein structure Structural Biology NLR Family Pyrin Domain-Containing 3 Protein Humans Death domain chemistry.chemical_classification 030102 biochemistry & molecular biology Chemistry Hydrogen bond Organic Chemistry Hydrogen Bonding computer.file_format Protein Data Bank Amino acid CARD Signaling Adaptor Proteins Molecular Docking Simulation Computational Mathematics 030104 developmental biology Ribonucleoproteins Docking (molecular) Biophysics Nanoparticles Apoptosis Regulatory Proteins computer Protein Binding |
| Zdroj: | Computational Biology and Chemistry |
| ISSN: | 1476-9271 |
| DOI: | 10.1016/j.compbiolchem.2018.04.013 |
| Popis: | The current research is based on computational study of the Death Domain (DD) superfamily of proteins involved in the cytoplasmic inflammasome complexes associated with apoptosis and inflammation in response to the nanoparticle treatment. The PYD domains of the DD superfamily proteins, NALP3 and ASC, were chosen for investigation as they are found to be primarily involved in the regulation of innate immunity and are associated with apoptosis and inflammation. The in-vitro studies of these proteins have proven to be a challenge as the proteins have a tendency to aggregate under laboratory conditions. The interactions between PYD-PYD domains of NALP3 & ASC proteins as well as PYD-PYD domains of NALP3 and ASC2 proteins were studied using the computational tools. In our study, the protein structures were taken from Protein Data Bank, and molecular dynamics simulation was performed using NAMD software followed by molecular docking studies using HADDOCK. The generated protein models were validated using PROCHECK and then the protein-protein interactions were analyzed using the molecular visualization tool CHIMERA. We noticed that the affinity between PYD of NALP3-ASC complex is better when compared to the NALP3-ASC2 complex based on their binding energies and docking scores. In the case of NALP3-ASC complex, seven key amino acids of ASC-PYD protein interface interact with four key amino acids of NALP3-PYD protein interface. However, in the case of NALP3-ASC2 complex, six key amino acids of ASC-PYD protein interact with four key amino acids of NALP3-PYD protein. Although, there is not much difference in the number of interacting amino acid residues between the two protein complexes, we understand that the NALP3-ASC exhibits better binding interaction and stability than the NALP3-ASC2 protein complex because the number of hydrogen bonding between them is more when compared to the latter. The hydrogen bonds between the interacting amino acids of the NALP3-ASC protein interface are 12, whereas it is 6 in the case of NALP3-ASC2 protein interaction. The protein-protein interaction seems to be dominated by the energetically significant hydrogen bonding followed by the electrostatic interaction in the NALP3-ASC protein interface, whereas both hydrogen bonding and the interaction between charged residues appears to play a significant role at the NALP3-ASC2 protein interfaces. |
| Databáze: | OpenAIRE |
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