Matter structured on a length scale comparable to or smaller than the wavelength of light can exhibit unusual optical properties. Particularly promising components for such materials are metal nanostructures, where structural alterations provide a straightforward means of tailoring their surface plasmon resonances and hence their interaction with light. But the top-down fabrication of plasmonic materials with controlled optical responses in the visible spectral range remains challenging, because lithographic methods are limited in resolution and in their ability to generate genuinely three-dimensional architectures. Molecular self-assembly provides an alternative bottom-up fabrication route not restricted by these limitations, and DNA- and peptide-directed assembly have proved to be viable methods for the controlled arrangement of metal nanoparticles in complex and also chiral geometries. Here we show that DNA origami enables the high-yield production of plasmonic structures that contain nanoparticles arranged in nanometre-scale helices. We find, in agreement with theoretical predictions, that the structures in solution exhibit defined circular dichroism and optical rotatory dispersion effects at visible wavelengths that originate from the collective plasmon-plasmon interactions of the nanoparticles positioned with an accuracy better than two nanometres. Circular dichroism effects in the visible part of the spectrum have been achieved by exploiting the chiral morphology of organic molecules and the plasmonic properties of nanoparticles, or even without precise control over the spatial configuration of the nanoparticles. In contrast, the optical response of our nanoparticle assemblies is rationally designed and tunable in handedness, colour and intensity-in accordance with our theoretical model.

A reconfigurable plasmonic nanosystem combines an active plasmonic structure with a regulated physical or chemical control input. There have been considerable e orts on integration of plasmonic nanostructures with active platforms using topdown techniques. The active media include phase-transition materials, graphene, liquid crystals and carrier-modulated semiconductors, which can respond to thermal 1 , electrical 2 and optical stimuli 3-5 . However, these plasmonic nanostructures are often restricted to two-dimensional substrates, showing desired optical response only along specific excitation directions. Alternatively, bottom-up techniques o er a new pathway to impart reconfigurability and functionality to passive systems. In particular, DNA has proven to be one of the most versatile and robust building blocks 6-9 for construction of complex three-dimensional architectures with high fidelity 10-14 . Here we show the creation of reconfigurable three-dimensional plasmonic metamolecules, which execute DNA-regulated conformational changes at the nanoscale. DNA serves as both a construction material to organize plasmonic nanoparticles in three dimensions, as well as fuel for driving the metamolecules to distinct conformational states. Simultaneously, the threedimensional plasmonic metamolecules can work as optical reporters, which transduce their conformational changes in situ into circular dichroism changes in the visible wavelength range.Circular dichroism (CD), that is, differential absorption of left-and right-handed circularly polarized light, of natural chiral macromolecules is highly sensitive to their three-dimensional (3D) conformations 15 . Taking a similar strategy, we create 3D reconfigurable plasmonic chiral metamolecules 4,16 , whose conformation changes are highly correlated with their pronounced and distinct CD spectral changes in the visible wavelength range. Figure 1a shows the design schematic. Two gold nanorods (AuNRs) are hosted on a reconfigurable DNA origami template 7,10 , which consists of two 14-helix bundles (80 nm × 16 nm × 8 nm) folded from a long single-stranded DNA (ssDNA) scaffold with the help of hundreds of staple strands 13 . The two origami bundles are linked together by the scaffold strand passing twice between them at one point. To ensure the mobility of the DNA bundles and avoid the formation of a Holliday junction 17 , 8 unpaired bases are introduced to each ssDNA connector (Supplementary Note 1). Twelve binding sites are extended from each origami bundle for robust assembly of one AuNR (38 nm × 10 nm) functionalized with complementary DNA (Supplementary Note 2). The surface to surface distance of the two AuNRs is roughly 25 nm. Owing to close proximity, the excited plasmons in the two AuNRs can be strongly coupled 18 . The two crossed AuNRs constitute a 3D plasmonic chiral object [19][20][21][22] , which generates a theme of handedness when interacting with left-and right-handed circularly polarized light, giving rise to strong CD. Left-handedRight-handed Two gold nanorods (...

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The self-assembly of nanoscale elements into three-dimensional structures with precise shapes and sizes is important in fields such as nanophotonics, metamaterials and biotechnology. Short molecular linkers have previously been used to create assemblies of nanoparticles, but the approach is limited to small interparticle distances, typically less than 10 nm. Alternatively, DNA origami can precisely organize nanoscale objects over much larger length scales. Here we show that rigid DNA origami scaffolds can be used to assemble metal nanoparticles, quantum dots and organic dyes into hierarchical nanoclusters that have a planet-satellite-type structure. The nanoclusters have a tunable stoichiometry, defined distances of 5-200 nm between components, and controllable overall sizes of up to 500 nm. We also show that the nanoscale components can be positioned along the radial DNA spacers of the nanostructures, which allows short- and long-range interactions between nanoparticles and dyes to be studied in solution. The approach could, in the future, be used to construct efficient energy funnels, complex plasmonic architectures, and porous, nanoengineered scaffolds for catalysis.