"Giant surfactants" created by the fast and efficient functionalization of a DNA tetrahedron with a temperature-responsive polymer.

ACS Nano 7:10 (2013) 8561-8572

Authors:

Thomas R Wilks, Jonathan Bath, Jan Willem de Vries, Jeffery E Raymond, Andreas Herrmann, Andrew J Turberfield, Rachel K O'Reilly

Abstract:

Copper catalyzed azide-alkyne cycloaddition (CuAAC) was employed to synthesize DNA block copolymers (DBCs) with a range of polymer blocks including temperature-responsive poly(N-isoproylacrylamide) (poly(NIPAM)) and highly hydrophobic poly(styrene). Exceptionally high yields were achieved at low DNA concentrations, in organic solvents, and in the absence of any solid support. The DNA segment of the DBC remained capable of sequence-specific hybridization: it was used to assemble a precisely defined nanostructure, a DNA tetrahedron, with pendant poly(NIPAM) segments. In the presence of an excess of poly(NIPAM) homopolymer, the tetrahedron-poly(NIPAM) conjugate nucleated the formation of large, well-defined nanoparticles at 40 °C, a temperature at which the homopolymer precipitated from solution. These composite nanoparticles were observed by dynamic light scattering and cryoTEM, and their hybrid nature was confirmed by AFM imaging. As a result of the large effective surface area of the tetrahedron, only very low concentrations of the conjugate were required in order for this surfactant-like behavior to be observed.

Optimizing DNA nanotechnology through coarse-grained modeling: a two-footed DNA walker.

ACS Nano 7:3 (2013) 2479-2490

Authors:

Thomas E Ouldridge, Rollo L Hoare, Ard A Louis, Jonathan PK Doye, Jonathan Bath, Andrew J Turberfield

Abstract:

DNA has enormous potential as a programmable material for creating artificial nanoscale structures and devices. For more complex systems, however, rational design and optimization can become difficult. We have recently proposed a coarse-grained model of DNA that captures the basic thermodynamic, structural, and mechanical changes associated with the fundamental process in much of DNA nanotechnology, the formation of duplexes from single strands. In this article, we demonstrate that the model can provide powerful insight into the operation of complex nanotechnological systems through a detailed investigation of a two-footed DNA walker that is designed to step along a reusable track, thereby offering the possibility of optimizing the design of such systems. We find that applying moderate tension to the track can have a large influence on the operation of the walker, providing a bias for stepping forward and helping the walker to recover from undesirable overstepped states. Further, we show that the process by which spent fuel detaches from the walker can have a significant impact on the rebinding of the walker to the track, strongly influencing walker efficiency and speed. Finally, using the results of the simulations, we propose a number of modifications to the walker to improve its operation.

Non-covalent single transcription factor encapsulation inside a DNA cage.

Angew Chem Int Ed Engl 52:8 (2013) 2284-2288

Authors:

Robert Crawford, Christoph M Erben, Javier Periz, Lucy M Hall, Tom Brown, Andrew J Turberfield, Achillefs N Kapanidis

Combinatorial displacement of DNA strands: application to matrix multiplication and weighted sums.

Angew Chem Int Ed Engl 52:4 (2013) 1189-1192

Authors:

Anthony J Genot, Jonathan Bath, Andrew J Turberfield

A clocked finite state machine built from DNA.

Chem Commun (Camb) 49:3 (2013) 237-239

Authors:

Cristina Costa Santini, Jonathan Bath, Andy M Tyrrell, Andrew J Turberfield

Abstract:

We implement a finite state machine by representing state, transition rules and input symbols with DNA components. Transitions between states are triggered by a clock signal which allows synchronized, parallel operation of two (or more) state machines. The state machine can be re-programmed by changing the input symbols.