
A research proposal to study the life cycle of COV
Author(s) -
Phelps Tin,
Sam Kunes
Publication year - 2021
Publication title -
journal of student research
Language(s) - English
Resource type - Journals
ISSN - 2167-1907
DOI - 10.47611/jsrhs.v10i2.1434
Subject(s) - viral life cycle , ura3 , computational biology , saccharomyces cerevisiae , drug discovery , biology , virus , yeast , computer science , genetics , bioinformatics , viral replication
SARS-CoV2 continues to affect the lives of the majority of the world, and although vaccines are beginning to become available, much of the world will still be unable to obtain them. Furthermore, some studies have suggested that there may have to be annual vaccines and as strains of the virus continue to increase, it is essential for us to move to the next stage of research and attempt to better understand the virus.
By utilizing a chemical genetics approach where numerous ligands of distinct chemical libraries are screened through high-throughput screening, we may be able to form an ordered viral cycle of metabolic events that could help identify drug targets more efficiently and coordinate drug use to improve efficacy. A modified version of the virus (to decrease its ability of infection) along with the URA3 protein is then inserted into yeast cells (Saccharomyces cerevisiae) and screened. A simple assay involving the addition of 5’- fluoroorotic acid helps to determine ligand interference and after identifying the compounds, we can order their action into specific steps in the lifecycle and order the events of the life cycle.