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Updated: Feb 10, 2026

Origami Inspired Self-assembly of Patterned and Reconfigurable Particles
Published on: February 4, 2013
Self-assembly of convex particles on spherocylindrical surfaces
Guillermo R Lázaro1, Bogdan Dragnea, Michael F Hagan
1Martin Fisher School of Physics, Brandeis University, Waltham, MA 02454, USA. hagan@brandeis.edu.
Precise control of protein and colloid self-assembly on curved surfaces is key for nanotechnology. Simulations show that matching subunit and template curvature is crucial for forming symmetrical nanostructures, guiding future material design.
Area of Science:
- Nanotechnology
- Materials Science
- Biophysics
Background:
- Controlling nanoscale self-assembly on curved surfaces is essential for developing advanced materials.
- Understanding protein and colloid behavior on non-planar substrates is a key challenge.
Purpose of the Study:
- To investigate the self-assembly of conical subunits on spherocylindrical templates.
- To develop a continuum theory for lattice bending energy on curved surfaces.
- To elucidate the role of curvature mismatch in dictating assembly outcomes.
Main Methods:
- Dynamical simulations of conical subunit self-assembly around spherocylindrical templates.
- Development of a continuum theory for bending energy of triangular lattices on arbitrary surfaces.
- Analysis of assembly on spherical and cylindrical cores to understand curvature effects.
Main Results:
- Assembly is highly sensitive to mismatches between subunit spontaneous curvature and template mean/anisotropic curvature.
- A regime of optimal assembly yielding symmetrical particles exists below a threshold curvature mismatch.
- Defective particle morphologies arise outside the optimal regime, dependent on the degree of mismatch.
- Both intrinsic (Gaussian) and extrinsic (mean) curvatures significantly guide anisotropic subunit assembly.
Conclusions:
- Curvature mismatch is a critical factor in protein and colloid self-assembly on curved templates.
- The findings provide a framework for designing nanoscale materials with controlled morphologies.
- Simulations accurately predict experimental observations of virus capsid protein assembly.
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