COVID-19 represents a new potentially life-threatening illness caused by severe acute respiratory syndrome coronavirus 2 or SARS-CoV-2 pathogen. In 2021, new variants of the virus with multiple key mutations have emerged, such as B.1.1.7, B.1.351, P.1 and B.1.617, and are threatening to render available vaccines or potential drugs ineffective. In this regard, we highlight 3CL pro , the main viral protease, as a valuable therapeutic target that possesses no mutations in the described pandemically relevant variants. 3CL pro could therefore provide trans-variant effectiveness that is supported by structural studies and possesses readily available biological evaluation experiments. With this in mind, we performed a high throughput virtual screening experiment using CmDock and the “ In-Stock ” chemical library to prepare prioritisation lists of compounds for further studies. We coupled the virtual screening experiment to a machine learning-supported classification and activity regression study to bring maximal enrichment and available structural data on known 3CL pro inhibitors to the prepared focused libraries. All virtual screening hits are classified according to 3CL pro inhibitor, viral cysteine protease or remaining chemical space based on the calculated set of 208 chemical descriptors. Last but not least, we analysed if the current set of 3CL pro inhibitors could be used in activity prediction and observed that the field of 3CL pro inhibitors is drastically under-represented compared to the chemical space of viral cysteine protease inhibitors. We postulate that this methodology of 3CL pro inhibitor library preparation and compound prioritisation far surpass the selection of compounds from available commercial “corona focused libraries”.
【저자키워드】 COVID-19, SARS-CoV-2, machine learning, Virtual screening, inhibitors, High-throughput, 3C-like protease, MPro, in silico drug design, 3CLpro, chemical library design, compound prioritisation, 【초록키워드】 Vaccine, coronavirus, Mutation, B.1.351, variant, drug, 3CL pro, protease, virus, variants, pathogen, B.1.1.7, P.1, B.1.617, Effectiveness, experiment, methodology, inhibitor, therapeutic target, acute respiratory syndrome, Compound, cysteine protease, highlight, described, performed, caused, analysed, supported, calculated, experiments, Last, potentially life-threatening, 【제목키워드】 3CL pro, development, Compound,