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وكيل كلية العلوم للتطوير و الجودة

كلية العلوم
قسم النبات و الاحياء الدقيقة / مكتب 2ب 49 الدور الثاني كلية العلوم مبنى 5
المنشورات
مقال فى مجلة
2025

An exploratory binding study of molnupiravir efficacy against emerging Omicron SARS-CoV-2 variants

SARS-CoV-2 (severe acute respiratory syndrome causing coronavirus 2) caused an epidemic that swept the globe and resulted in large number of casualties. It is still sporadically causing cases and has a long-term impact on the health of once infected individuals. Molnupiravir binds RNA dependent RNA polymerase (RdRp) of SARS-CoV-2 as well as spike protein. In this study, we assessed the mutated spike protein of BA.5 variant and BQ.1.1 subvariant of COVID-19 and tested their binding with it. Multiple sequence and structural alignment of homologous structures revealed highly conserved amino acid residues at the active site of the domain. The molecular docking of Molnupiravir with the active site of the domain, comprised conserved motifs (motif A-G), and exhibited considerable binding affinity against variant and subvariant protein targets. Molnupiravir exhibited stability in its interactions with the Omicron and BQ.1.1 spike proteins, preserving constant engagement within the active site. The protein and Ligand reached An equilibrium with An RMSD of 10.46 & Aring; after 100 nanoseconds, whereas the Ligand measured 8.0 & Aring;. Fluctuations were noted between 40 And 75 nanoseconds, stabilizing from 80 to 100 ns. In simulations including the BQ.1.1 subvariant, the RMSD values demonstrated considerable stability, exhibiting Little variations. The ligand demonstrated flexibility, altering its binding orientation over time, resulting in An average RMSD of 18.72 & Aring;. Herein, investigation of molecular dynamics trajectories elucidated the conformational stability of Molnupiravir, emphasizing its interactions with active residues and the hydrogen bond acceptor and donor environments. The results highlighted the crucial function of protein loops in offering flexibility and enabling ligand binding within the active site. It is concluded that Molnupiravir has the potential to function as an inhibitor of both omicron and its subvariant BQ.1.1.

اسم الناشر
NATURE PORTFOLIO
مدينة النشر
BERLIN
رقم المجلد
15
رقم الانشاء
1
مزيد من المنشورات
publications

SARS-CoV-2 (severe acute respiratory syndrome causing coronavirus 2) caused an epidemic that swept the globe and resulted in large number of casualties. It is still sporadically causing cases and…

بواسطة Ahmad, Faisal; Basharat, Zarrin; Janjua, Ayesha; Najmi, Muzammil Hasan; Almajhdi, Fahad Nasser; Hussain, Tajamul; Ozsahin, Dilber Uzun; Waheed, Yasir
2025
تم النشر فى:
NATURE PORTFOLIO
publications
بواسطة Almuqrin, Abdulaziz M.; Aziz, Ibrahim M.; Alrezaihi, Abdulrahman F.; Alzamil, Lama; Farrag, Mohamed A.; Hafiz, Taghreed A.; Aljowaie, Reem M.; Almajhdi, Fahad N.
2025
تم النشر فى:
BMC
publications

The global pandemic caused by severe acute respiratory syndrome coronavirus 2 ;(SARS-CoV-2) severely affects a tremendous number of people worldwide, imposing a heavy economic burden.AimThis study…

بواسطة 2. Farrag, M. A., Aljowaie, R. M., Alzayed, R. M., Aziz, I. M., Alhajouj, S. A., Alaboudi, K. A. N., … Almajhdi, F. N.
2025