| Literature DB >> 32913117 |
Josue San Emeterio1, Lois Pollack2.
Abstract
Despite the threat to human health posed by some single-stranded RNA viruses, little is understood about their assembly. The goal of this work is to introduce a new tool for watching an RNA genome direct its own packaging and encapsidation by proteins. Contrast variation small-angle X-ray scattering (CV-SAXS) is a powerful tool with the potential to monitor the changing structure of a viral RNA through this assembly process. The proteins, though present, do not contribute to the measured signal. As a first step in assessing the feasibility of viral genome studies, the structure of encapsidated MS2 RNA was exclusively detected with CV-SAXS and compared with a structure derived from asymmetric cryo-EM reconstructions. Additional comparisons with free RNA highlight the significant structural rearrangements induced by capsid proteins and invite the application of time-resolved CV-SAXS to reveal interactions that result in efficient viral assembly.Entities:
Keywords: RNA folding; RNA structure; RNA virus; X-ray scattering; bacteriophage MS2; contrast variation SAXS; plus-stranded RNA virus; small-angle X-ray scattering (SAXS); virus assembly; virus structure
Year: 2020 PMID: 32913117 PMCID: PMC7681021 DOI: 10.1074/jbc.RA120.013961
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157