Molecular dynamic study of SARS-CoV-2 with various S protein mutations and their effect on thermodynamic properties. (February 2022)

• Record Type: Journal Article
• Authors: Abdalla, Mohnad; Eltayb, Wafa Ali; El-Arabey, Amr Ahmed; Singh, Kamal; Jiang, Xinyi
• Is Part Of: Computers in biology and medicine. Volume 141(2022)
• Publication Date: 2022-02
• Subjects: SARS-CoV-2 -- Variant -- S protein -- MD simulation; Medicine -- Data processing -- Periodicals; Biology -- Data processing -- Periodicals; 610.285
• DOI: 10.1016/j.compbiomed.2021.105025
• Languages: English
• ISSNs: 0010-4825

Abstract

Abstract: Studying the structure of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike (S) protein is important to understand the infection process. The S protein is necessary in completing the virus life cycle and is responsible for the appearance of new variants and drug and vaccine resistance. Understanding the structure and dynamics of biological macromolecules is essential for understanding how they function. In this work, we investigated the effects of mutations on S protein stability and solubility through molecular dynamic (MD) simulation in a 100 ns (ns) period. We screened four variants in addition to the wild type (WT). Results show that changes on MD simulation parameters of S protein indicate fluctuations and changes in the conformation, especially in the area between 300 and 600 amino acids (aa). This provides us an image of how the virus protein can reshape itself to adapt to any changes that occur in human angiotensin-converting enzyme 2 or drugs that can target the protein region. Our results also show that the Brazil variant has high fluctuations and unstable folding at some stages compared with other variants. Highlights: MD simulation parameters of S protein indicate fluctuations and changes in the conformation, especially in the area between 300 and 600 amino acids. The SARS-CoV-2 S protein has the ability to rearrange itself in response to changes in human angiotensin-converting enzyme 2 or drugs that target the protein region. Brazil variant has high fluctuations and unstable folding at some stages compared with other variants.