Structural biology of SARS-CoV-2 accessory proteins

The coronavirus SARS-CoV-2 is the causative agent for the COVID-19 pandemic. Its proteome is typically separated into three classes of proteins: (1) Structural proteins which facilitate the transport and host cell infiltration of the viral RNA, (2) non-structural proteins which are thought to be essential for the viral life cycle and are all produced from open reading frame 1ab (ORF1ab) on the RNA, and (3) everything else, called accessory proteins. Although it was originally thought that these accessory proteins are non-essential for viral replication, a growing body of evidence suggests that these diverse proteins have crucial roles in virus-host interactions, in particular in the way they interfere with the signalling pathways that modulate the host cell's response to infection and viral pathogenicity. Here, we summarize efforts to structurally characterize the accessory proteins from SARS-CoV-2.

Automated summary

The coronavirus SARS-CoV-2 is categorized into three classes of proteins: structural proteins, non-structural proteins, and accessory proteins. While accessory proteins were initially considered non-essential for viral replication, there is increasing evidence suggesting their crucial roles in virus-host interactions by interfering with host cell signaling pathways. This article summarizes the efforts to structurally characterize the accessory proteins of SARS-CoV-2.