Molnupiravir'in Covid-19'a Karşı Moleküler Kenetlenme ve Moleküler Dinamik Simülasyonları

Year 2024, Volume: 12 Issue: 2, 134 - 141, 30.12.2024

Tugce Sinem Oktemer , Zeynep Önem , Sefa Çelik , Ayşen Özel , Sevim Akyüz

https://doi.org/10.18586/msufbd.1563429

Abstract

COVID-19 tedavisinde kullanılan molnupiravir'in (C13H19N3O7) en kararlı konformasyonu Spartan06 programı ile belirlenmiştir. CAVER programı kullanılarak, spike glikoprotein, ACE2 reseptörü ve COVID-19'un ana proteaz enziminin (Mpro) apo ve holo formlarına ait potansiyel aktif bağlanma bölgeleri tanımlanmıştır. Molnupiravir'in hedef reseptörlere bağlanma afinitesini belirlemek için Autodock Vina kullanılarak moleküler kenetlenme analizleri gerçekleştirilmiştir. Molnupiravir'in spike glikoprotein (PDB ID: 6VXX), ACE2 (PDB ID: 6M0J; 1R42), apo formu (PDB ID: 6M03) ve COVID-19 M^pro'nun holo formu (PDB ID: 6LU7) ile moleküler kenetlenme hesaplamalarının sonuçları sırasıyla -7,8, -7,7, -7,7, -7,1 ve -7,4 kcal/mol'de güçlü bağlanma afinitesi göstermiştir. Ayrıca, ligand-reseptör etkileşimlerini daha detaylı incelemek amacıyla molnupiravirin ACE2 (1R42) ile en yüksek skor alan ligand-reseptör kompleksinin 50 ns MD simülasyonu yapılmıştır.

Keywords

molnupiravir, ACE2, Spike glycoprotein, Moleküler Kenetlenme, Moleküler Dinamik

Molecular Docking and Molecular Dynamics Simulations of Molnupiravir Against Covid-19

Abstract

The most stable conformation of molnupiravir (C13H19N3O7), which is frequently used in the COVID-19 treatment, was elucidated by the Spartan06 program. Using the CAVER program, the potential active binding sites that belong to the spike glycoprotein, ACE2 receptor, and both the apo and holo forms of the main protease enzyme(Mpro) of COVID-19 were identified. To determine the binding affinity of molnupiravir to target receptors, molecular docking analyses were carried out using Autodock Vina. The results of molecular docking calculations of the molnupiravir with the spike glycoprotein (PDB ID:6VXX), ACE2 (PDB ID:6M0J;1R42), the apo form (PDB ID: 6M03) and the holo form of COVID-19 Mpro (PDB ID: 6LU7) showed strong binding affinities at -7.8, -7.7, -7.7, -7.1, and -7.4 kcal/mol, respectively. Moreover, top-scoring ligand-receptor complex of the molnupiravir with ACE2 (1R42) were subjected to 50 ns all-atom MD simulations to investigate the ligand-receptor interactions in more detail.

Keywords

molnupiravir, ACE2, Spike glycoprotein, Molecular docking, Molecular dynamics

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