Homology Modeling and Molecular Dynamics Studies of EC1 Domain of VE-Cadherin to Elucidate Docking Interaction with Cadherin-Derived Peptide  

Oleh:

Prasasty, Vivitri Dewi ; Tambunan, Usman Sumo Friend ; Siahaan, Teruna Jaya

Jenis: Article from Journal - e-Journal
Dalam koleksi: Online Journal of Biological Science vol. 14 no. 02 (2014), page 155-162.
Topik: VE-Cadherin; Blood Brain Barrier; Homology Modeling; Molecular Dynamics; Molecular Docking
Fulltext: ojbsci_14_02_05_Prasasty.pdf (288.91KB)

Isi artikel

VE-cadherin is a protein in the cadherin family that is found at the adherens junctions of the microvessel endothelial cells of the Blood-Brain Barrier (BBB). It is recognized as the homotypic cell adhesion molecules and there is limited structural information on how VE-cadherins mediate cell-cell adhesion. It has been shown that the EC1 domain of cadherins is important for the homophilic interactions for cell-cell adhesion. Therefore, the aims of this study are to model the structure of the EC1 domain of VE-cadherin, study its molecular dynamics properties and evaluate its interactions with cadherin peptides. In this study, the sequence alignment between EC1 domain of VE-cadherin and the template protein were conducted by CLUSTALW2 platform. The SWISS-MODEL platform performed the homology modeling of the EC1 domain of VE-cadherin structure. Structural refinement was done by using KOBAMIN. Some validation analysis platforms also were conducted included PROCHECK, VERIFY3D, ERRAT and MOLPROBITY to check the allowed residues region in Ramachandran Plot (RP) and the quality of the structure. The most favored region was found 95.5% in RP value and overall model structure quality is 71.34%. Molecular Dynamics (MD) was run under CABS-FLEX to determine the flexibility of the residue index. The RMSD value of MD is 1.5Å per residue index. Eventually, molecular docking by AUTODOCK VINA was conducted to investigate protein-ligand interaction. From docking, it is found that the affinity energy is -4.8 kcal/mol which has the most favorable binding of EC1 domain with the peptide.

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