Research

Visual abstract of the Barnes DNP lab

Our laboratory applies improvements in magnetic resonance spectroscopy to biomolecular structure determination.  Solid state nuclear magnetic resonance (NMR) is exquisitely suited to probe atomic level structural detail of biomolecules not amendable to x-ray crystallography.  However, the small nuclear magnetic moments that yield narrow resonances also result in very low inherent sensitivity in NMR. Dynamic Nuclear Polarization (DNP) is a powerful combined electron paramagnetic resonance (EPR) and NMR technique that transfers the strong polarization from unpaired electron spins to nuclear spins to boost NMR sensitivity.  In our DNP experiments, we employ frequency agile gyrotrons, and extreme cryogenic sample cooling to increase the sensitivity of solid state NMR experiments up to a factor of 20,000. This tremendous gain in sensitivity results in acquiring data 400 million times faster than conventional NMR experiments and will have a profound impact on magnetic resonance spectroscopy and structural biology.  The drastic gain in sensitivity will permit biomolecular structure determination in complex heterogeneous systems in vitro with less than a milligram of sample and in hours of experimental time, or directly in vivo in a cellular context without protein purification.

Spectrum of 13C labled Urea with and without microwaves

Dynamic Nuclear Polarization Instrumentation and Methodology:  We are developing a novel frequency tunable gyrotron capable of changing the frequency output on a microsecond time scale. Microwave frequency agility will permit the development of advanced spectroscopic irradiation schemes on the electron spins during the DNP experiment and yield significantly more control over the DNP Hamiltonian, and much more sensitive NMR experiments.  We also build our own NMR DNP probes, which can couple both high-power radio frequency and microwave power simultaneously to the sample that is spinning at the magic angle (54.7 deg) with respect to the magnetic field.  Remarkably, the NMR probe also cools our samples to 20-90 Kelvin with cryogenic helium and nitrogen, which is required to extend the relaxation times of both the electron and nuclear magnetic moments.

In vivo NMR, Bryostatin, Protein Kinase C, and HIV/AIDS Eradication:  Our laboratory is invested in determining biomolecular structure and dynamics required to design new potent and non-toxic drugs to reverse HIV latency.  The activation of such latent reservoirs is one promising strategy towards the erradicaiton of HIV/AIDS.  Our sensitive magnetic resonance instrumentation and associated methodology will be employed to drive drug development efforts of bryostatin, a powerful activator of Protein Kinase C (PKC).  Improved bryostatin analogs that can selectively target specific pathways downstream of PKC will have tremendously important implications, ranging from eradicating HIV/AIDS to new treatments to combat Alzheimer’s and cancer.  For instance, bryostatin can activate latent viral reservoirs of HIV through binding to Protein Kinase C.  Further development of bryostatin and similar drugs are crucial to exposing infected HIV T-cells that currently escape destruction from current anti-retroviral HIV therapy.  The applications of our technology development and enhanced structure determination techniques have even wider applications to virtually every protein, molecule, and chemical architecture of structural interest to biomedical science.