Case Study of High-Throughput Drug Screening and Remote Data Collection for SARS-CoV-2 Main Protease by Using Serial Femtosecond X-ray Crystallography
Authors:
- Omur GuvenOGOmur Guven
- Mehmet GulMehmet Gul
- Esra AyanEAEsra Ayan
- J Austin JohnsonJJJ Austin Johnson
- Baris CakilkayaBaris Cakilkaya
- Gozde UstaGUGozde Usta
- Fatma Betul ErtemFEFatma Betul Ertem
- Nurettin TokayNTNurettin Tokay
- Busra YukselBYBusra Yuksel
- Oktay GocenlerOGOktay Gocenler
- Cengizhan BuyukdagCBCengizhan Buyukdag
- Sabine BothaSBSabine Botha
Open Access
Abstract
Since early 2020, COVID-19 has grown to affect the lives of billions globally. A worldwide investigation has been ongoing for characterizing the virus and also for finding an effective drug and developing vaccines. As time has been of the essence, a crucial part of this research has been drug repurposing; therefore, confirmation of in silico drug screening studies have been carried out for this purpose. Here we demonstrated the possibility of screening a variety of drugs efficiently by leveraging a high data collection rate of 120 images/second with the new low-noise, high dynamic range ePix10k2M Pixel Array Detector installed at the Macromolecular Femtosecond Crystallography (MFX) instrument at the Linac Coherent Light Source (LCLS). The X-ray Free-Electron Laser (XFEL) is used for remote high-throughput data collection for drug repurposing of the main protease (Mpro) of SARS-CoV-2 at ambient temperature with mitigated X-ray radiation damage. We obtained multiple structures soaked with nine drug candidate molecules in two crystal forms. Although our drug binding attempts failed, we successfully established a high-throughput Serial Femtosecond X-ray crystallographic (SFX) data collection protocol.Keywords
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