Zinc plays a crucial role in the process of virion maturation inside the host cell. The accessory Cys-rich proteins expressed in SARS-CoV-2 by genes ORF7a and ORF8 are likely involved in zinc binding and in interactions with cellular antigens activated by extensive disulfide bonds. Starting from a proof-of-concept [1], we are now using computational models and X-ray absorption spectroscopy for a structural study of orf7a and orf8 proteins in contact with the BST2 tetherin protein. A conceivable hypothesis is that lack of cellular zinc, or substitution thereof, might lead to a significant slowing down of viral maturation.

SARS-CoV-2 Virion Stabilization by Zn Binding

Morante S;La Penna G;
2020

Abstract

Zinc plays a crucial role in the process of virion maturation inside the host cell. The accessory Cys-rich proteins expressed in SARS-CoV-2 by genes ORF7a and ORF8 are likely involved in zinc binding and in interactions with cellular antigens activated by extensive disulfide bonds. Starting from a proof-of-concept [1], we are now using computational models and X-ray absorption spectroscopy for a structural study of orf7a and orf8 proteins in contact with the BST2 tetherin protein. A conceivable hypothesis is that lack of cellular zinc, or substitution thereof, might lead to a significant slowing down of viral maturation.
2020
SARS-CoV-2; zinc; intrinsically disordered proteins
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/384536
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