284 research outputs found
Optimal self-assembly of finite shapes at temperature 1 in 3D
Working in a three-dimensional variant of Winfree's abstract Tile Assembly
Model, we show that, for an arbitrary finite, connected shape , there is a tile set that uniquely self-assembles into a 3D
representation of a scaled-up version of at temperature 1 in 3D with
optimal program-size complexity (the "program-size complexity", also known as
"tile complexity", of a shape is the minimum number of tile types required to
uniquely self-assemble it). Moreover, our construction is "just barely" 3D in
the sense that it only places tiles in the and planes. Our
result is essentially a just-barely 3D temperature 1 simulation of a similar 2D
temperature 2 result by Soloveichik and Winfree (SICOMP 2007)
Self-Assembly of 4-sided Fractals in the Two-handed Tile Assembly Model
We consider the self-assembly of fractals in one of the most well-studied
models of tile based self-assembling systems known as the Two-handed Tile
Assembly Model (2HAM). In particular, we focus our attention on a class of
fractals called discrete self-similar fractals (a class of fractals that
includes the discrete Sierpi\'nski carpet). We present a 2HAM system that
finitely self-assembles the discrete Sierpi\'nski carpet with scale factor 1.
Moreover, the 2HAM system that we give lends itself to being generalized and we
describe how this system can be modified to obtain a 2HAM system that finitely
self-assembles one of any fractal from an infinite set of fractals which we
call 4-sided fractals. The 2HAM systems we give in this paper are the first
examples of systems that finitely self-assemble discrete self-similar fractals
at scale factor 1 in a purely growth model of self-assembly. Finally, we show
that there exists a 3-sided fractal (which is not a tree fractal) that cannot
be finitely self-assembled by any 2HAM system
Reflections on Tiles (in Self-Assembly)
We define the Reflexive Tile Assembly Model (RTAM), which is obtained from
the abstract Tile Assembly Model (aTAM) by allowing tiles to reflect across
their horizontal and/or vertical axes. We show that the class of directed
temperature-1 RTAM systems is not computationally universal, which is
conjectured but unproven for the aTAM, and like the aTAM, the RTAM is
computationally universal at temperature 2. We then show that at temperature 1,
when starting from a single tile seed, the RTAM is capable of assembling n x n
squares for n odd using only n tile types, but incapable of assembling n x n
squares for n even. Moreover, we show that n is a lower bound on the number of
tile types needed to assemble n x n squares for n odd in the temperature-1
RTAM. The conjectured lower bound for temperature-1 aTAM systems is 2n-1.
Finally, we give preliminary results toward the classification of which finite
connected shapes in Z^2 can be assembled (strictly or weakly) by a singly
seeded (i.e. seed of size 1) RTAM system, including a complete classification
of which finite connected shapes be strictly assembled by a "mismatch-free"
singly seeded RTAM system.Comment: New results which classify the types of shapes which can
self-assemble in the RTAM have been adde
Optimization of supply diversity for the self-assembly of simple objects in two and three dimensions
The field of algorithmic self-assembly is concerned with the design and
analysis of self-assembly systems from a computational perspective, that is,
from the perspective of mathematical problems whose study may give insight into
the natural processes through which elementary objects self-assemble into more
complex ones. One of the main problems of algorithmic self-assembly is the
minimum tile set problem (MTSP), which asks for a collection of types of
elementary objects (called tiles) to be found for the self-assembly of an
object having a pre-established shape. Such a collection is to be as concise as
possible, thus minimizing supply diversity, while satisfying a set of stringent
constraints having to do with the termination and other properties of the
self-assembly process from its tile types. We present a study of what we think
is the first practical approach to MTSP. Our study starts with the introduction
of an evolutionary heuristic to tackle MTSP and includes results from extensive
experimentation with the heuristic on the self-assembly of simple objects in
two and three dimensions. The heuristic we introduce combines classic elements
from the field of evolutionary computation with a problem-specific variant of
Pareto dominance into a multi-objective approach to MTSP.Comment: Minor typos correcte
Programmable disorder in random DNA tilings
Scaling up the complexity and diversity of synthetic molecular structures will require strategies that exploit the inherent stochasticity of molecular systems in a controlled fashion. Here we demonstrate a framework for programming random DNA tilings and show how to control the properties of global patterns through simple, local rules. We constructed three general forms of planar network—random loops, mazes and trees—on the surface of self-assembled DNA origami arrays on the micrometre scale with nanometre resolution. Using simple molecular building blocks and robust experimental conditions, we demonstrate control of a wide range of properties of the random networks, including the branching rules, the growth directions, the proximity between adjacent networks and the size distribution. Much as combinatorial approaches for generating random one-dimensional chains of polymers have been used to revolutionize chemical synthesis and the selection of functional nucleic acids, our strategy extends these principles to random two-dimensional networks of molecules and creates new opportunities for fabricating more complex molecular devices that are organized by DNA nanostructures
DNA-based Self-Assembly of Chiral Plasmonic Nanostructures with Tailored Optical Response
Surface plasmon resonances generated in metallic nanostructures can be
utilized to tailor electromagnetic fields. The precise spatial arrangement of
such structures can result in surprising optical properties that are not found
in any naturally occurring material. Here, the designed activity emerges from
collective effects of singular components equipped with limited individual
functionality. Top-down fabrication of plasmonic materials with a predesigned
optical response in the visible range by conventional lithographic methods has
remained challenging due to their limited resolution, the complexity of
scaling, and the difficulty to extend these techniques to three-dimensional
architectures. Molecular self-assembly provides an alternative route to create
such materials which is not bound by the above limitations. We demonstrate how
the DNA origami method can be used to produce plasmonic materials with a
tailored optical response at visible wavelengths. Harnessing the assembly power
of 3D DNA origami, we arranged metal nanoparticles with a spatial accuracy of 2
nm into nanoscale helices. The helical structures assemble in solution in a
massively parallel fashion and with near quantitative yields. As a designed
optical response, we generated giant circular dichroism and optical rotary
dispersion in the visible range that originates from the collective
plasmon-plasmon interactions within the nanohelices. We also show that the
optical response can be tuned through the visible spectrum by changing the
composition of the metal nanoparticles. The observed effects are independent of
the direction of the incident light and can be switched by design between left-
and right-handed orientation. Our work demonstrates the production of complex
bulk materials from precisely designed nanoscopic assemblies and highlights the
potential of DNA self-assembly for the fabrication of plasmonic nanostructures.Comment: 5 pages, 4 figure
Placement and orientation of individual DNA shapes on lithographically patterned surfaces
Artificial DNA nanostructures show promise for the organization of functional materials to create nanoelectronic or nano-optical devices. DNA origami, in which a long single strand of DNA is folded into a shape using shorter 'staple strands', can display 6-nm-resolution patterns of binding sites, in principle allowing complex arrangements of carbon nanotubes, silicon nanowires, or quantum dots. However, DNA origami are synthesized in solution and uncontrolled deposition results in random arrangements; this makes it difficult to measure the properties of attached nanodevices or to integrate them with conventionally fabricated microcircuitry. Here we describe the use of electron-beam lithography and dry oxidative etching to create DNA origami-shaped binding sites on technologically useful materials, such as SiO_2 and diamond-like carbon. In buffer with ~ 100 mM MgCl_2, DNA origami bind with high selectivity and good orientation: 70–95% of sites have individual origami aligned with an angular dispersion (±1 s.d.) as low as ±10° (on diamond-like carbon) or ±20° (on SiO_2)
- …