DNA-Guided Assembly of Nanocellulose Meshes.

Nanoengineered materials are a product of joint collaboration of theoreticians and experimentalists, of physicists, (bio-)chemists, and recently, of computer scientists. In the field of Nanotechnology and Nanoengineering, DNA (algorithmic) self-assembly has an acknowledged leading position. As a fabric, DNA is a rather inferior material; as a medium for shape, pattern, and dynamic behavior reconstruction, it is one of the most versatile nanomaterials. This is why the prospect of combining the physical properties of known high performance nanomaterials, such as cellulose, graphene, or fibroin, with the assembly functionality of DNA scaffolds is a very promising prospect. In this work we analyze the dynamical and structural properties of a would-be DNA-guided assembly of nanocellulose meshes. The aim is to generate pre-experimental insights on possible ways of manipulating structural properties of such meshes. The mechanistic principles of these systems, implemented through the DNA assembly apparatus, ensure the formation of 2D nanocellulose mesh structures. A key desired feature for such an engineered synthetic material, e.g. with applications in bio-medicine and nano-engineering, would be to control the size of the openings (gaps) within these meshes, a.k.a. its aperture. However, in the case of this composite material, this is not a direct engineered feature. Rather, we assert it could be indirectly achieved through varying several key parameters of the system. We consider here several experimentally tunable parameters, such as the ratio between nanocellulose fibrils and the DNA guiding elements, i.e., aptamer-functionalized DNA origamis, as well as the assumed length of the nanocellulose fibrils. To this aim, we propose a computational model of the mesh-assembly dynamical system, which we subject to numerical parameter scan and analysis.