Revealing the Structural Plasticity of SARS-CoV‑2 nsp7 and nsp8 Using Structural Proteomics
Loading...
Date
Authors
Courouble, V.V.
Dey, S.K.
Yadav, R.
Timm, J.
Harrison, J.J.E.K.
Ruiz, F.X.
Arnold, E.
Griffin, P.R.
Journal Title
Journal ISSN
Volume Title
Publisher
Abstract
Coronavirus (CoV) nonstructural proteins (nsps)
assemble to form the replication−transcription complex (RTC)
responsible for viral RNA synthesis. nsp7 and nsp8 are important
cofactors of the RTC, as they interact and regulate the activity of
RNA-dependent RNA polymerase and other nsps. To date, no
structure of the full-length SARS-CoV-2 nsp7:nsp8 complex has
been published. The current understanding of this complex is
based on structures from truncated constructs, with missing
electron densities, or from related CoV species where SARS-CoV-2
nsp7 and nsp8 share upward of 90% sequence identity. Despite
available structures solved using crystallography and cryo-EM
representing detailed static snapshots of the nsp7:nsp8 complex, it
is evident that the complex has a high degree of structural
plasticity. However, relatively little is known about the conformational dynamics of the individual proteins and how they complex to
interact with other nsps. Here, the solution-based structural proteomic techniques, hydrogen−deuterium exchange mass
spectrometry (HDX-MS) and cross-linking mass spectrometry (XL-MS), illuminate the dynamics of SARS-CoV-2 full-length nsp7
and nsp8 proteins and the nsp7:nsp8 protein complex. Results presented from the two techniques are complementary and validate
the interaction surfaces identified from the published three-dimensional heterotetrameric crystal structure of the SARS-CoV-2
truncated nsp7:nsp8 complex. Furthermore, mapping of XL-MS data onto higher-order complexes suggests that SARS-CoV-2 nsp7
and nsp8 do not assemble into a hexadecameric structure as implied by the SARS-CoV full-length nsp7:nsp8 crystal structure.
Instead, our results suggest that the nsp7:nsp8 heterotetramer can dissociate into a stable dimeric unit that might bind to nsp12 in
the RTC without significantly altering nsp7−nsp8 interactions.
Description
Research Article
