AI Article Synopsis

  • SARS-CoV-2 is the virus responsible for the global COVID-19 pandemic, first recognized in March 2020 by WHO, leading to the development of various vaccines and treatments.
  • Despite these advancements, variants like Delta and Omicron pose ongoing challenges, indicating the need for improved therapies and understanding of immune responses.
  • The focus of current research includes exploring the molecular interactions between SARS-CoV-2 and human cells, particularly how its spike protein interacts with ACE2 receptors, potential viral receptors, and the implications for vaccine effectiveness and protein synthesis in infected cells.

Article Abstract

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the causative agent of the devastating global COVID-19 pandemic announced by WHO in March 2020. Through unprecedented scientific effort, several vaccines, drugs and antibodies have been developed, saving millions of lives, but the fight against COVID-19 continues as immune escape variants of concern such as Delta and Omicron emerge. To develop more effective treatments and to elucidate the side effects caused by vaccines and therapeutic agents, a deeper understanding of the molecular interactions of SARS-CoV-2 with them and human cells is required. With special interest in computational approaches, we will focus on the structure of SARS-CoV-2 and the interaction of its spike protein with human angiotensin-converting enzyme-2 (ACE2) as a prime entry point of the virus into host cells. In addition, other possible viral receptors will be considered. The fusion of viral and human membranes and the interaction of the spike protein with antibodies and nanobodies will be discussed, as well as the effect of SARS-CoV-2 on protein synthesis in host cells.

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Source
http://dx.doi.org/10.1039/d1cs01170gDOI Listing

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