Journal
JOURNAL OF MOLECULAR CELL BIOLOGY
Volume 15, Issue 3, Pages -Publisher
OXFORD UNIV PRESS
DOI: 10.1093/jmcb/mjad021
Keywords
SARS-CoV-2 spike; allosteric modulation; D-NEMD simulations; fatty acid binding site; SARS-CoV-2 variants
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The spike protein of SARS-CoV-2 contains a fatty acid binding site that is functionally important. Removing the fatty acid can significantly affect the conformation and functionality of the spike protein. Different variants of SARS-CoV-2 have varying responses to the removal of the fatty acid, indicating potential differences in transmissibility and virulence. Experimental comparison of the effects of the fatty acid on different variants is necessary.
The SARS-CoV-2 spike protein contains a functionally important fatty acid (FA) binding site, which is also found in some other coronaviruses, e.g. SARS-CoV and MERS-CoV. The occupancy of the FA site by linoleic acid (LA) reduces infectivity by 'locking' the spike in a less infectious conformation. Here, we use dynamical-nonequilibrium molecular dynamics (D-NEMD) simulations to compare the allosteric responses of spike variants to LA removal. D-NEMD simulations show that the FA site is coupled to other functional regions of the protein, e.g. the receptor-binding motif (RBM), N-terminal domain (NTD), furin cleavage site, and regions surrounding the fusion peptide. D-NEMD simulations also identify the allosteric networks connecting the FA site to these functional regions. The comparison between the wild-type spike and four variants (Alpha, Delta, Delta plus, and Omicron BA.1) shows that the variants differ significantly in their responses to LA removal. The allosteric connections to the FA site on Alpha are generally similar to those on the wild-type protein, with the exception of the RBM and the S71-R78 region, which show a weaker link to the FA site. In contrast, Omicron is the most different variant, exhibiting significant differences in the RBM, NTD, V622-L629, and furin cleavage site. These differences in the allosteric modulation may be of functional relevance, potentially affecting transmissibility and virulence. Experimental comparison of the effects of LA on SARS-CoV-2 variants, including emerging variants, is warranted.
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