A positive-feedback mechanism promotes reovirus particle conversion to the intermediate associated with membrane penetration
- 29 July 2008
- journal article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 105 (30) , 10571-10576
- https://doi.org/10.1073/pnas.0802039105
Abstract
Membrane penetration by reovirus is associated with conversion of a metastable intermediate, the ISVP, to a further-disassembled particle, the ISVP*. Factors that promote this conversion in cells are poorly understood. Here, we report the in vitro characterization of a positive-feedback mechanism for promoting ISVP* conversion. At high particle concentration, conversion approximated second-order kinetics, and products of the reaction operated in trans to promote the conversion of target ISVPs. Pore-forming peptide mu1N, which is released from particles during conversion, was sufficient for promoting activity. A mutant that does not undergo mu1N release failed to exhibit second-order conversion kinetics and also failed to promote conversion of wild-type target ISVPs. Susceptibility of target ISVPs to promotion in trans was temperature dependent and correlated with target stability, suggesting that capsid dynamics are required to expose the interacting epitope. A positive-feedback mechanism of promoting escape from the metastable intermediate has not been reported for other viruses but represents a generalizable device for sensing a confined volume, such as that encountered during cell entry.Keywords
This publication has 57 references indexed in Scilit:
- Peptides released from reovirus outer capsid form membrane pores that recruit virus particlesThe EMBO Journal, 2008
- Thermolabilizing Pseudoreversions in Reovirus Outer-Capsid Protein μ1 Rescue the Entry Defect Conferred by a Thermostabilizing MutationJournal of Virology, 2007
- Thermostabilizing mutations in reovirus outer-capsid protein μ1 selected by heat inactivation of infectious subvirion particlesVirology, 2007
- Mammalian reovirus, a nonfusogenic nonenveloped virus, forms size-selective pores in a model membraneProceedings of the National Academy of Sciences, 2006
- Features of Reovirus Outer Capsid Protein μ1 Revealed by Electron Cryomicroscopy and Image Reconstruction of the Virion at 7.0 Å ResolutionStructure, 2005
- Putative Autocleavage of Reovirus μ1 Protein in Concert with Outer-capsid Disassembly and Activation for Membrane PermeabilizationJournal of Molecular Biology, 2005
- The δ Region of Outer-Capsid Proteinμ1 Undergoes Conformational Change and Release from ReovirusParticles during CellEntryJournal of Virology, 2003
- Thermostability of Reovirus Disassembly Intermediates (ISVPs) Correlates with Genetic, Biochemical, and Thermodynamic Properties of Major Surface Protein μ1Journal of Virology, 2002
- Complete In Vitro Assembly of the Reovirus Outer Capsid Produces Highly Infectious Particles Suitable for Genetic Studies of the Receptor-Binding ProteinJournal of Virology, 2001
- Early steps in reovirus infection are associated with dramatic changes in supramolecular structure and protein conformation: analysis of virions and subviral particles by cryoelectron microscopy and image reconstructionThe Journal of cell biology, 1993