Single-stranded RNA viruses co-assemble their capsid with the genome, and variations in capsid structures can have significant functional relevance. In particular, viruses need to respond to a dehydrating environment to prevent genomic degradation and remain active upon rehydration. Theoretical work has predicted low-energy buckling transitions in icosahedral capsids, which could protect the virus from further dehydration. However, there has been no direct experimental evidence, nor a molecular mechanism, for such behavior. Here, we observe this transition using X-ray single particle imaging of MS2 bacteriophages after aerosolization. Using a combination of machine learning tools, we classify hundreds of thousands of single-particle diffraction patterns to learn the structural landscape of the capsid morphology as a function of time spent in the aerosol phase. We found a previously unreported compact conformation as well as intermediate structures that suggest an incoherent buckling transition that does not preserve icosahedral symmetry. Finally, we propose a mechanism for this buckling, where a single 19-residue loop is destabilized, leading to the large observed morphological change. Our results provide experimental evidence for a mechanism by which viral capsids may protect themselves from dehydration upon aerosolization. In the process, these findings also demonstrate the power of single-particle X-ray imaging and machine learning methods in studying biomolecular structural dynamics.
Mall et al. (Tue,) studied this question.