Molecular insights into the complex mechanics of plant epidermal cell walls

Plants have evolved complex nanofibril-based cell walls to meet diverse biological and physical constraints. How strength and extensibility emerge from the nanoscale-to-mesoscale organization of growing cell walls has long been unresolved. We sought to clarify the mechanical roles of cellulose and matrix polysaccharides by developing a coarse-grained model based on polymer physics that recapitulates aspects of assembly and tensile mechanics of epidermal cell walls. Simple noncovalent binding interactions in the model generate bundled cellulose networks resembling that of primary cell walls and possessing stress-dependent elasticity, stiffening, and plasticity beyond a yield threshold. Plasticity originates from fibril-fibril sliding in aligned cellulose networks. This physical model provides quantitative insight into fundamental questions of plant mechanobiology and reveals design principles of biomaterials that combine stiffness with yielding and extensibility.

Automated summary

Plants have evolved complex nanofibril-based cell walls to meet diverse biological and physical constraints, with cellulose and matrix polysaccharides playing important mechanical roles. By simulating the assembly and tensile mechanics of cell walls, researchers found that fibril-fibril sliding in cellulose networks leads to plasticity, revealing design principles of biomaterials.