| Literature DB >> 27511920 |
Yue Liu1, Marchel G Hill2, Thomas Klose1, Zhenguo Chen1, Kelly Watters2, Yury A Bochkov3, Wen Jiang1, Ann C Palmenberg4, Michael G Rossmann5.
Abstract
Isolates of rhinovirus C (RV-C), a recently identified Enterovirus (EV) species, are the causative agents of severe respiratory infections among children and are linked to childhood asthma exacerbations. The RV-C have been refractory to structure determination because they are difficult to propagate in vitro. Here, we report the cryo-EM atomic structures of the full virion and native empty particle (NEP) of RV-C15a. The virus has 60 "fingers" on the virus outer surface that probably function as dominant immunogens. Because the NEPs also display these fingers, they may have utility as vaccine candidates. A sequence-conserved surface depression adjacent to each finger forms a likely binding site for the sialic acid on its receptor. The RV-C, unlike other EVs, are resistant to capsid-binding antiviral compounds because the hydrophobic pocket in VP1 is filled with multiple bulky residues. These results define potential molecular determinants for designing antiviral therapeutics and vaccines.Entities:
Keywords: asthma; atomic structure; cryoelectron microscopy; rhinovirus C
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Year: 2016 PMID: 27511920 PMCID: PMC4987780 DOI: 10.1073/pnas.1606595113
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205