The study of antiviral drugs targeting SARS-CoV-2 nucleocapsid and spike proteins through large-scale compound repurposing.

ABSTRACT: Contributing to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) clinical treatment, a drug library encompassing approximately 3,142 clinical-stage or FDA-approved small molecules is profiled to identify the candidate therapeutic inhibitors targeting nucleocapsid protein (N) and spike protein (S) of SARS-CoV-2. 16 screened candidates with higher binding affinity are evaluated via virtual screening. Comparing to those under trial/temporarily used antivirus drugs (i.e., umifenovir, lopinavir), ceftriaxone, cefotaxime, and cefuroxime show higher binding affinities to the N-terminal domain of N protein (N-NTD), C-terminal domain of N protein (N-CTD), and receptor-binding domain of S protein (S-RBD). Cefotaxime and cefuroxime have high binding affinities towards S-RBD with angiotensin-converting enzyme 2 (ACE2) complex via influence the critical interface sites at the interface of S-RBD (Arg⁴⁰³, Tyr⁴⁵³, Trp⁴⁹⁵, Gly⁴⁹⁶, Phe⁴⁹⁷, Asn⁵⁰¹and Tyr⁵⁰⁵) and ACE2 (Asn³³, His³⁴, Glu³⁷, Asp³⁸, Lys³⁵³, Ala³⁸⁶, Ala³⁸⁷, Gln³⁸⁸, Pro³⁸⁹, Phe³⁹⁰ and Arg³⁹³) complex.

SUBMITTER: Hu X 

PROVIDER: S-EPMC7919521 | biostudies-literature | 2021 Mar

REPOSITORIES: biostudies-literature