Assembly and Architecture of Gram-Positive and -Negative Cell Walls
Abstract
The cell wall, a porous mesh-like structure, provides shape and physical protection for bacteria. At the atomic level, it is composed of peptidoglycan (PG), a polymer of stiff glycan strands cross-linked by short, flexible peptides. However, at the mesoscale, multiple models for the organization of PG have been put forth, distinguished by glycan strands parallel to the cell surface (the so-called "layered'' model) or perpendicular (the "scaffold" model). To test these models, and to resolve the mechanical properties of PG, we have built and simulated at an atomic scale patches of both Gram-positive and negative cell walls in different organizations up to 50 nanometers in size. In the case of Gram-positive PG, molecular dynamics simulations of the layered model are found to elucidate the mechanisms behind a distinct curling effect observed in three-dimensional electron cryo-tomography images of fragmented cell walls. For Gram-negative PG, simulations of patches with different average-glycan-strand lengths reveal an anisotropic elasticity, in good agreement with atomic-force microscopy experiments. Insights from the simulations reveal how mesoscopic and macroscopic properties of a ubiquitous bacterial ultrastructure arise from its atomic-scale interactions and organization.
Additional Information
© 2013 Biophysical Society. Published by Elsevier Inc.Attached Files
Published - 1-s2.0-S000634951204790X-main.pdf
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- Eprint ID
- 38121
- Resolver ID
- CaltechAUTHORS:20130425-135202813
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2013-05-03Created from EPrint's datestamp field
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2021-11-09Created from EPrint's last_modified field