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In most synthetic self-assembly processes the size of the final structure grows unbound and is only limited by the number of accessible microscopic building blocks. In comparison, biological assemblies can autonomously regulate their size and shape. One mechanism for such self-regulation is based on the chirality of microscopic units. Chirality induces a twisted geometry of building blocks that is incompatible with long-ranged crystalline packing, thereby stopping the assembly’s growth at a given stage. Chiral self-regulating self-assemblies, based on thermodynamic equilibration rather than kinetic trapping, remain an elusive target that has attracted considerable attention. So far studies of chiral self-assembly processes have focused on non-responsive systems, whose equilibrium points are not easily shifted in situ, which limits their versatility and applicability. Here, we demonstrate stimuli-responsive self-regulating self-assembly. This assembly is composed of chiral and magnetically alignable nanorods, where the effective chirality is modulable by balancing chirality-induced twisting with magnet-induced untwisting alignment. Changing the magnetic field intensity, controls the strength of self-regulation, leading to assemblies whose sizes and shapes are rationally controlled. The described size/shape control mechanism is tunable, reversible, robust, and widely applicable, opening up new possibilities for generating biomimetics structures with desirable functions and properties.
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This content will become publicly available on December 1, 2025
Developmental assembly of multi-component polymer systems through interconnected synthetic gene networks in vitro
Living cells regulate the dynamics of developmental events through interconnected signaling systems that activate and deactivate inert precursors. This suggests that similarly, synthetic biomaterials could be designed to develop over time by using chemical reaction networks to regulate the availability of assembling components. Here we demonstrate how the sequential activation or deactivation of distinct DNA building blocks can be modularly coordinated to form distinct populations of self-assembling polymers using a transcriptional signaling cascade of synthetic genes. Our building blocks are DNA tiles that polymerize into nanotubes, and whose assembly can be controlled by RNA molecules produced by synthetic genes that target the tile interaction domains. To achieve different RNA production rates, we use a strategy based on promoter “nicking” and strand displacement. By changing the way the genes are cascaded and the RNA levels, we demonstrate that we can obtain spatially and temporally different outcomes in nanotube assembly, including random DNA polymers, block polymers, and as well as distinct autonomous formation and dissolution of distinct polymer populations. Our work demonstrates a way to construct autonomous supramolecular materials whose properties depend on the timing of molecular instructions for self-assembly, and can be immediately extended to a variety of other nucleic acid circuits and assemblies.
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- Award ID(s):
- 2107483
- PAR ID:
- 10635055
- Publisher / Repository:
- Springer Nature
- Date Published:
- Journal Name:
- Nature Communications
- Volume:
- 15
- Issue:
- 1
- ISSN:
- 2041-1723
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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