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Ground state instabilities of protein shells are eliminated by buckling
- Source :
- Soft Matter. 13:8300-8308
- Publication Year :
- 2017
- Publisher :
- Royal Society of Chemistry (RSC), 2017.
-
Abstract
- We propose a hybrid discrete-continuum model to study the ground state of protein shells. The model allows for shape transformation of the shell and buckling transitions as well as the competition between states with different symmetries that characterize discrete particle models with radial pair potentials. Our main results are as follows. For large Föppl-von Kármán (FvK) numbers the shells have stable isometric ground states. As the FvK number is reduced, shells undergo a buckling transition resembling that of thin-shell elasticity theory. When the width of the pair potential is reduced below a critical value, then buckling coincides with the onset of structural instability triggered by over-stretched pair potentials. Chiral shells are found to be more prone to structural instability than achiral shells. It is argued that the well-width appropriate for protein shells lies below the structural instability threshold. This means that the self-assembly of protein shells with a well-defined, stable structure is possible only if the bending energy of the shell is sufficiently low so that the FvK number of the assembled shell is above the buckling threshold.
- Subjects :
- Models, Molecular
0301 basic medicine
Nuclear Theory
Shell (structure)
Bending
01 natural sciences
Instability
03 medical and health sciences
0103 physical sciences
Physics::Atomic and Molecular Clusters
010306 general physics
Mechanical Phenomena
Physics
Protein Stability
Proteins
Stereoisomerism
General Chemistry
Condensed Matter Physics
Critical value
Biomechanical Phenomena
030104 developmental biology
Classical mechanics
Buckling
Homogeneous space
Thermodynamics
Ground state
Pair potential
Subjects
Details
- ISSN :
- 17446848 and 1744683X
- Volume :
- 13
- Database :
- OpenAIRE
- Journal :
- Soft Matter
- Accession number :
- edsair.doi.dedup.....b3e57018ccea1ff0142dc83bd305148b
- Full Text :
- https://doi.org/10.1039/c7sm01184a