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SARS-CoV-2 Omicron subvariant spike N405 unlikely to rapidly deamidate.

Authors :
Beaudoin, Christopher A.
Petsolari, Emmanouela
Hamaia, Samir W.
Hala, Sharif
Alofi, Fadwa S.
Pandurangan, Arun P.
Blundell, Tom L.
Chaitanya Vedithi, Sundeep
Huang, Christopher L.-H.
Jackson, Antony P.
Source :
Biochemical & Biophysical Research Communications. Jul2023, Vol. 666, p61-67. 7p.
Publication Year :
2023

Abstract

The RGD motif on the SARS-CoV-2 spike protein has been suggested to interact with RGD-binding integrins αVβ3 and α5β1 to enhance viral cell entry and alter downstream signaling cascades. The D405N mutation on the Omicron subvariant spike proteins, resulting in an RGN motif, has recently been shown to inhibit binding to integrin αVβ3. Deamidation of asparagines in protein ligand RGN motifs has been demonstrated to generate RGD and RGisoD motifs that permit binding to RGD-binding integrins. Two asparagines, N481 and N501, on the Wild-type spike receptor-binding domain have been previously shown to have deamidation half-lives of 16.5 and 123 days, respectively, which may occur during the viral life cycle. Deamidation of Omicron subvariant N405 may recover the ability to interact with RGD-binding integrins. Thus, herein, all-atom molecular dynamics simulations of the Wild-type and Omicron subvariant spike protein receptor-binding domains were conducted to investigate the potential for asparagines, the Omicron subvariant N405 in particular, to assume the optimized geometry for deamidation to occur. In summary, the Omicron subvariant N405 was primarily found to be stabilized in a state unfavourable for deamidation after hydrogen bonding with downstream E406. Nevertheless, a small number of RGD or RGisoD motifs on the Omicron subvariant spike proteins may restore the ability to interact with RGD-binding integrins. The simulations also provided structural clarification regarding the deamidation rates of Wild-type N481 and N501 and highlighted the utility of tertiary structure dynamics information in predicting asparagine deamidation. Further work is needed to characterize the effects of deamidation on spike-integrin interactions. • The deamidation mechanisms of Wild-type N481 and N501 were further elucidated. • Hydrogen bonding and backbone constraints interfere with Omicron N405 deamidation. • The Q498R mutation affects potential deamidation of distant asparagines. • Slow deamidation of N405 may result in a mixture of spike protein RGD/RGisoD motifs. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
0006291X
Volume :
666
Database :
Academic Search Index
Journal :
Biochemical & Biophysical Research Communications
Publication Type :
Academic Journal
Accession number :
163945750
Full Text :
https://doi.org/10.1016/j.bbrc.2023.04.088