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post it note DNA

Dr Jon Bath

Group Leader

Research theme

  • Biological physics

Sub department

  • Condensed Matter Physics

Research groups

  • Nucleic acid nanotechnology
jonathan.bath@physics.ox.ac.uk
Biochemistry Building, room 30-092
  • About
  • Publications

DNA origami dimensions and structure measured by solution X-ray scattering

EUROPEAN BIOPHYSICS JOURNAL WITH BIOPHYSICS LETTERS 46 (2017) S137-S137

Authors:

MA Baker, AJ Tuckwell, JF Berengut, J Bath, F Benn, AP Duff, AE Whitten, KE Dunn, RM Hynson, AJ Turberfield, LK Lee
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DNA-templated peptide assembly

EUROPEAN BIOPHYSICS JOURNAL WITH BIOPHYSICS LETTERS 46 (2017) S303-S303

Authors:

J Jin, EG Baker, J Bath, DN Woolfson, AJ Turberfield
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An Autonomous Molecular Assembler for Programmable Chemical Synthesis.

Nature Chemistry Nature Publishing Group (2016)

Authors:

Meng, RA Muscat, ML McKee, PJ Milnes, El-Sagheer, JN Bath, Davis, Brown, RK O'Reilly, Turberfield

Abstract:

Molecular machines that assemble polymers in a programmed sequence are fundamental to life. They are also an achievable goal of nanotechnology. Here, we report synthetic molecular machinery made from DNA which controls and records the formation of covalent bonds. We show that an autonomous cascade of DNA hybridization reactions can create oligomers, from building blocks linked by olefin or peptide bonds, with a sequence defined by a reconfigurable molecular program. The system can also be programmed to achieve combinatorial assembly. The sequence of assembly reactions, and thus the structure, of each oligomer synthesized is recorded in a DNA molecule which enables this information to be recovered by PCR amplification followed by DNA sequencing.
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Precision control of DNA-based molecular reactions

Institution of Engineering and Technology (IET) (2016) 1 .-1 .

Authors:

TE Ouldridge, JS Schreck, F Romano, P Sulc, RF Machinek, NEC Haley, AA Louis, JPK Doye, J Bath, AJ Turberfield
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Modelling DNA origami self-assembly at the domain level.

Journal of Chemical Physics AIP Publishing 143:16 (2015) 165102

Authors:

Frits Dannenberg, Katherine E Dunn, Jonathan Bath, Marta Kwiatkowska, Andrew J Turberfield, Thomas E Ouldridge

Abstract:

We present a modelling framework, and basic model parameterization, for the study of DNA origami folding at the level of DNA domains. Our approach is explicitly kinetic and does not assume a specific folding pathway. The binding of each staple is associated with a free-energy change that depends on staple sequence, the possibility of coaxial stacking with neighbouring domains, and the entropic cost of constraining the scaffold by inserting staple crossovers. A rigorous thermodynamic model is difficult to implement as a result of the complex, multiply connected geometry of the scaffold: we present a solution to this problem for planar origami. Coaxial stacking of helices and entropic terms, particularly when loop closure exponents are taken to be larger than those for ideal chains, introduce interactions between staples. These cooperative interactions lead to the prediction of sharp assembly transitions with notable hysteresis that are consistent with experimental observations. We show that the model reproduces the experimentally observed consequences of reducing staple concentration, accelerated cooling, and absent staples. We also present a simpler methodology that gives consistent results and can be used to study a wider range of systems including non-planar origami.
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