In this work, we assess a previously advanced hypothesis that predicts the existence of ion channels in the capsid of small and non-enveloped icosahedral viruses. With this purpose we examine Triatoma Virus (TrV) as a case study. This virus has a stable capsid under highly acidic conditions but disassembles and releases the genome in alkaline environments. Our calculations range from a subtle sub-atomic proton interchange to the dismantling of a large-scale system representing several million of atoms. Our results provide structure-based explanations for the three roles played by the capsid to enable genome release. First, we observe, for the first time, the formation of a hydrophobic gate in the cavity along the five-fold axis of the wild-...
Knowledge about structure and dynamics of the important biological macromolecules — proteins, nuclei...
Triatoma virus (TrV), a positive-sense ssRNA virus with a small spherical non-enveloped capsid of ~3...
AbstractThe M2 protein of influenza virus forms ion channels activated by low pH which are proton pe...
In this work, we assess a previously advanced hypothesis that predicts the existence of ion channels...
In this work, we assess a previously advanced hypothesis that predicts the existence of ion channels...
Even though viruses evolve mainly in liquid milieu, their horizontal transmission routesoften includ...
The interaction between a viral capsid and its genome governs crucial steps in the life cycle of a v...
In viruses, uncoating and RNA release are two key steps of successfully infecting a target cell. Dur...
Even though viruses evolve mainly in liquid milieu, their horizontal transmission routes often inclu...
For a three dimensional structure to spontaneously self-assemble from many identical components it m...
Dissolution of many plant viruses is thought to start with swelling of the capsid caused by calcium ...
The M2 protein of influenza virus forms ion channels activated by low pH which are proton permeable ...
9 pags, 6 figs. -- Supplementary material associated with this article can be found, in the online ...
We present the results of Molecular Dynamics simulations of a viral capsid with the aim to analyse i...
The M2 protein is a small, single-span transmembrane (TM) protein from the influenza A virus. This v...
Knowledge about structure and dynamics of the important biological macromolecules — proteins, nuclei...
Triatoma virus (TrV), a positive-sense ssRNA virus with a small spherical non-enveloped capsid of ~3...
AbstractThe M2 protein of influenza virus forms ion channels activated by low pH which are proton pe...
In this work, we assess a previously advanced hypothesis that predicts the existence of ion channels...
In this work, we assess a previously advanced hypothesis that predicts the existence of ion channels...
Even though viruses evolve mainly in liquid milieu, their horizontal transmission routesoften includ...
The interaction between a viral capsid and its genome governs crucial steps in the life cycle of a v...
In viruses, uncoating and RNA release are two key steps of successfully infecting a target cell. Dur...
Even though viruses evolve mainly in liquid milieu, their horizontal transmission routes often inclu...
For a three dimensional structure to spontaneously self-assemble from many identical components it m...
Dissolution of many plant viruses is thought to start with swelling of the capsid caused by calcium ...
The M2 protein of influenza virus forms ion channels activated by low pH which are proton permeable ...
9 pags, 6 figs. -- Supplementary material associated with this article can be found, in the online ...
We present the results of Molecular Dynamics simulations of a viral capsid with the aim to analyse i...
The M2 protein is a small, single-span transmembrane (TM) protein from the influenza A virus. This v...
Knowledge about structure and dynamics of the important biological macromolecules — proteins, nuclei...
Triatoma virus (TrV), a positive-sense ssRNA virus with a small spherical non-enveloped capsid of ~3...
AbstractThe M2 protein of influenza virus forms ion channels activated by low pH which are proton pe...