Protein-Assisted Large-Scale Assembly and Differential Patterning of DNA Origami Lattices

Nanofabrication has experienced a big boost with the invention of DNA origami, enabling the production and assembly of complex nanoscale structures that may be able to unlock fully new functionalities in biology and beyond. The remarkable precision with which these structures can be designed and produced is, however, not yet matched by their assembly dynamics, which can be extremely slow, particularly when attached to biological templates, such as membranes. Here, the rapid and controlled formation of DNA origami lattices on the scale of hundreds of micrometers in as little as 30 minutes is demonstrated, utilizing active patterning by the E.coli Min protein system, thereby yielding a remarkable improvement over conventional passive diffusion-based assembly methods. Various patterns, including spots, inverse spots, mazes, and meshes can be produced at different scales, tailored through the shape and density of the assembled structures. The differential positioning accomplished by Min-induced diffusiophoresis even allows the introduction of "pseudo-colors", i.e., complex core-shell patterns, by simultaneously patterning different DNA origami species. Beyond the targeted functionalization of biological surfaces, this approach may also be promising for applications in plasmonics, catalysis, and molecular sensing. DNA origami revolutionized nanofabrication, allowing precise assembly of nanostructures. Despite this, large-scale assembly remains challenging. The authors present a breakthrough: the rapid and controlled formation of DNA origami lattices using the Min protein system. Achieving large-scale lattices in just 30 minutes, this method outperforms conventional diffusion-based approaches. Multiple patterns and core-shell architectures open up possibilities for advanced functionalization with various applications.image