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The glycoprotein quality control factor Malectin promotes coronavirus replication and viral protein biogenesis
Jonathan Davies
Lars Plate
Acceso Abierto
Atribución-NoComercial-SinDerivadas
https://doi.org/10.1101/2024.06.02.597051
https://www.biorxiv.org/content/10.1101/2024.06.02.597051v1
Coronaviruses (CoV) rewire host protein homeostasis (proteostasis) networks through interactions between viral nonstructural proteins (nsps) and host factors to promote infection. With the emergence of SARS-CoV-2, it is imperative to characterize host interactors shared across nsp homologs. Using quantitative proteomics and functional genetic screening, we identify conserved proteostasis interactors of nsp2 and nsp4 that serve pro-viral roles during infection of murine hepatitis virus (MHV) – a model betacoronavirus. We uncover a glycoprotein quality control factor, Malectin (MLEC), which significantly reduces infectious titers when knocked down. During infection, nsp2 interacts with MLEC-associated proteins and the MLEC-interactome is drastically altered, stabilizing association with the Oligosaccheryltransferase (OST) complex, a crucial component of viral glycoprotein production. MLEC promotes viral protein levels and genome replication through its quality control activity. Lastly, we show MLEC promotes SARS-CoV-2 replication. Our results reveal a role for MLEC in mediating CoV infection and identify a potential target for pan-CoV antivirals
bioRxiv
03-06-2024
Preimpreso
Inglés
Público en general
VIRUS RESPIRATORIOS
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