March 18, 2021American Association for the Advancement of Science
In an analysis that explores the structural underpinnings of a SARS-CoV-2 strain, G614, that quickly became dominant early in the pandemic, researchers discovered interactions that prevent this strain's spike protein from shedding its host binding domain too early.
This may explain the enhanced infectivity of the G614 virus, they say.
Throughout the COVID-19 pandemic, epidemiologists have monitored evolution of the SARS-CoV-2 virus with particular focus on the spike (S) protein. Spike trimers decorate the viral surface and facilitate host cell entry.
An early variant with a single-residue substitution (G614) in its spike protein rapidly became the dominant strain throughout the world, and studies have also suggested it is more infectious than the original strain.
Puzzlingly, studies have shown that it does not bind more tightly to recombinant ACE2, the host cell receptor.
In the current study, the researchers investigated the structural basis for the spread of the G614 virus. Structural and biochemical studies using cryo-electron microscopy on a full-length G614 S trimer revealed interactions not present in D614, the original strain, which was described earlier in a paper published in Science in July 2020.
In particular, a loop wedges between domains in the G614 spike, in an added interaction that appears to stabilize the spike to prevent premature dissociation of the G614 trimer.
This effectively increases the number of functional spikes. "[W]e suggest that the enhanced infectivity of the G614 virus largely results from the increased stability of the S trimer," conclude the authors.
The research could help inform future COVID-19 vaccine development.
- This press release was provided by the American Association for the Advancement of Science