Sensitivity Enhancement and Hyperpolarisation

NMR is inherently insensitive. This is because the interaction of nuclear magnetic moments with an applied magnetic field is extremely small. The situation is dramatically worse for nuclei with low natural abundance of their magnetically-active isotopes, such as carbon-13 (1.1%), nitrogen-15 (0.37%) and silicon-29 (4.67%). I am interested in developing methods which can be used to improve the sensitivity of NMR spectroscopy, both as a tool for structure elucidation and to probe biologically interesting problems.

Photo-Chemically Induced Dynamic Nuclear Polarisation is a technique whereby a spin-state selective chemical reaction is used to generate nuclear polarisation. In principle any reaction which proceeds via a radical pair intermediate can be used. Typically, we have employed the photochemical reaction between a flavin and the aromatic amino acid side chains of tyrosine, tryptophan and histidine. This nuclear polarisation has then been used to study protein folding and to probe the structure of partially folding or denatured proteins.

Dynamic Nuclear Polarisation is a technique nearly as old as NMR spectroscopy itself. It relies on the transfer of polarisation from an unpaired electron in a cryogenic solid to the nuclei of interest. This project was in collaboration with Oxford Instruments and Pfizer, Ltd. We have developed methods using this heteronuclear hyperpolarisation, such as the co-acquisition of carbon-13 and nitrogen-15 polarisation and the measurement of heteronuclear spin-lattice relaxation times, on a timescale only relying on the time required to generate the nuclear hyperpolarisation.

Key publications

  1. K. H. Mok, L. T. Kuhn, M. Goez, I. J. Day, J. C. Lin, N. H. Andersen, and P. J. Hore.
    A pre-exisiting hydrophobic collapse in the unfolded state of an ultrafast folding protein.
    Nature, 447(7140):106-109, 2007. [ DOI ]
  2. K. H. Mok, T. Nagashima, I. J. Day, P. J. Hore, and C. M. Dobson.
    Multiple subsets of side-chain packing in partially folded states of α-lactalbumins.
    Proc. Natl. Acad. Sci. USA, 102(25):8899-8904, 2005. [ DOI ]
  3. I. J. Day, J. C. Mitchell, M. J. Snowden, and A. L. Davis.
    Applications of DNP-NMR for the measurement of heteronuclear T1 relaxation times.
    J. Magn. Reson., 187(2):216-224, 2007. [ DOI ]
  4. I. J. Day, J. C. Mitchell, M. J. Snowden, and A. L. Davis.
    Co-acquisition of hyperpolarised 13C and 15N NMR spectra.
    Magn. Reson. Chem., 45(12):1018-1021, 2007. [ DOI ]