Increasing valence pushes DNA nanostar networks to the isostatic point
Author(s) -
Nathaniel Conrad,
Tynan Kennedy,
Deborah Kuchnir Fygenson,
Omar A. Saleh
Publication year - 2019
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.1819683116
Subject(s) - rubber elasticity , materials science , shear modulus , elasticity (physics) , nonlinear system , valence (chemistry) , strain hardening exponent , elastic modulus , nanomechanics , modulus , natural rubber , composite material , mechanics , nanotechnology , physics , atomic force microscopy , quantum mechanics
Significance Maxwell (1864) predicted that 3D networks of beams fixed to junctions through freely rotating joints will be rigid only if at least six beams emanate from each junction. This concept is key to macroscopic design of trussed structures, but its relevance to microscopic networks, where thermal fluctuations are large, such as in biomolecular gels, is not as clear. Here, we exploit DNA nanotechnology to create gels of defined connectivity and demonstrate that gel mechanics are controlled by an interplay between entropic effects, network structure, and Maxwell’s rigidity criterion.
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