TY - JOUR T1 - Structure of the 5’ untranslated region in SARS-CoV-2 genome and its specific recognition by innate immune system via the human oligoadenylate synthase 1<sup>†</sup> JF - bioRxiv DO - 10.1101/2021.12.10.472066 SP - 2021.12.10.472066 AU - Emmanuelle Bignon AU - Tom Miclot AU - Alessio Terenzi AU - Giampaolo Barone AU - Antonio Monari Y1 - 2022/01/01 UR - http://biorxiv.org/content/early/2022/01/11/2021.12.10.472066.abstract N2 - 2’-5’-Oligoadenylate synthetase 1 (OAS1) is one of the key enzymes driving the innate immune system response to SARS-CoV-2 infection whose activity has been related to COVID-19 severity. In particular, OAS1 is a sensor of endogenous RNA that triggers the 2’-5’ oligoadenylate/RNase L pathway in response to viral infections, ultimately activating the RNA-Lyase which cleaves endogenous and exogenous RNA impeding the viral maturation. Upon SARS-CoV-2 infection, OAS1 is responsible for the recognition of viral RNA and has been shown to possess a particularly high sensitivity for the 5’-untranslated (5’-UTR) RNA region, which is organized in a double-strand stem loop motif (SLA). Since the structure of the nucleic acid/protein complex has not been resolved, here we report its structure obtained by molecular modeling, including enhanced sampling approaches. We also pinpoint that the SL1 region enhances the interaction network with the enzyme, promoting specific hydrogen bonds, absent in normal double strand RNA fragments, hence rationalizing the high affinity for OAS1.Competing Interest StatementThe authors have declared no competing interest. ER -