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The Oxford 750MHz NMR Spectrometer

The Oxford 750MHz NMR Spectrometer

Prof Jonathan Jones

Professor of Physics

Research theme

  • Quantum information and computation

Sub department

  • Atomic and Laser Physics

Research groups

  • NMR quantum computing
jonathan.jones@physics.ox.ac.uk
  • About
  • Publications

Quantum Computing with NMR

(2010)

Magnetic field sensors using 13-spin cat states

Physical Review A Atomic Molecular and Optical Physics 82:2 (2010)

Authors:

S Simmons, JA Jones, SD Karlen, A Ardavan, JJL Morton

Abstract:

Measurement devices could benefit from entangled correlations to yield a measurement sensitivity approaching the physical Heisenberg limit. Building upon previous magnetometric work using pseudoentangled spin states in solution-state NMR, we present two conceptual advancements to better prepare and interpret the pseudoentanglement resource. We apply these to a 13-spin cat state to measure the local magnetic field with a 12.2 sensitivity increase over an equivalent number of isolated spins. 漏 2010 The American Physical Society.

Preparing pseudo-pure states with controlled-transfer gates

(2010)

Authors:

Minaru Kawamura, Benjamin Rowland, Jonathan A Jones

Group epitope mapping considering relaxation of the ligand (GEM-CRL): including longitudinal relaxation rates in the analysis of saturation transfer difference (STD) experiments.

J Magn Reson 203:1 (2010) 1-10

Authors:

Sebastian Kemper, Mitul K Patel, James C Errey, Benjamin G Davis, Jonathan A Jones, Timothy DW Claridge

Abstract:

In the application of saturation transfer difference (STD) experiments to the study of protein-ligand interactions, the relaxation of the ligand is one of the major influences on the experimentally observed STD factors, making interpretation of these difficult when attempting to define a group epitope map (GEM). In this paper, we describe a simplification of the relaxation matrix that may be applied under specified experimental conditions, which results in a simplified equation reflecting the directly transferred magnetisation rate from the protein onto the ligand, defined as the summation over the whole protein of the protein-ligand cross-relaxation multiplied by with the fractional saturation of the protein protons. In this, the relaxation of the ligand is accounted for implicitly by inclusion of the experimentally determined longitudinal relaxation rates. The conditions under which this "group epitope mapping considering relaxation of the ligand" (GEM-CRL) can be applied were tested on a theoretical model system, which demonstrated only minor deviations from that predicted by the full relaxation matrix calculations (CORCEMA-ST) [7]. Furthermore, CORCEMA-ST calculations of two protein-saccharide complexes (Jacalin and TreR) with known crystal structures were performed and compared with experimental GEM-CRL data. It could be shown that the GEM-CRL methodology is superior to the classical group epitope mapping approach currently used for defining ligand-protein proximities. GEM-CRL is also useful for the interpretation of CORCEMA-ST results, because the transferred magnetisation rate provides an additional parameter for the comparison between measured and calculated values. The independence of this parameter from the above mentioned factors can thereby enhance the value of CORCEMA-ST calculations.

Spin-selective reactions of radical pairs act as quantum measurements

(2010)

Authors:

Jonathan A Jones, Peter J Hore

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