Quantitative [Fe]MRI of PSMA-targeted SPIONs specifically discriminates among prostate tumor cell types based on their PSMA expression levels

Laurel O Sillerud BRaIN Center, Department of Neurology, University of New Mexico School of Medicine, Albuquerque, NM, USA Abstract: We report the development, experimental verification, and application of a general theory called [Fe]MRI (pronounced fem-ree) for the non-invasive, quantitative molecular magnetic resonance imaging (MRI) of added magnetic nanoparticles or other magnetic contrast agents in biological tissues and other sites. [Fe]MRI can easily be implemented on any MRI instrument, requiring only measurements of the background nuclear magnetic relaxation times (T1, T2) of the tissue of interest, injection of the magnetic particles, and the subsequent acquisition of a pair of T1-weighted and T2-weighted images. These images, converted into contrast images, are subtracted to yield a contrast difference image proportional to the absolute nanoparticle, iron concentration, ([Fe]) image. [Fe]MRI was validated with the samples of superparamagnetic iron oxide nanoparticles (SPIONs) both in agarose gels and bound to human prostate tumor cells. The [Fe]MRI measurement of the binding of anti-prostate specific membrane antigen (PSMA) conjugated SPIONs to PSMA-positive LNCaP and PSMA-negative DU145 cells in vitro allowed a facile discrimination among prostate tumor cell types based on their PSMA expression level. The low [Fe] detection limit of ~2 µM for SPIONs allows sensitive MRI of added iron at concentrations considerably below the US Food and Drug Administration’s human iron dosage guidelines (<90 µM, 5 mg/kg). Keywords: contrast difference, RT-PCR, flow cytometr

External high-Quality-factor Resonator tunes up nuclear magnetic resonance

The development of powerful sensors for the detection of weak electromagnetic fields is crucial for many spectroscopic applications, in particular for nuclear magnetic resonance (NMR). Here, we present a comprehensive theoretical model for boosting the NMR signal-to-noise ratio, validated by liquid-state 1H, 129Xe and 6Li NMR experiments at low frequencies, using an external resonator with a high quality-factor combined with a low-quality-factor input coil. In addition to an enhanced signal-to-noise ratio, this approach exhibits striking features such as a high degree of flexibility with respect to input coil parameters and a square-root dependence on the sample volume, and signifies an important step towards compact NMR spectroscopy at low frequencies with small and large coils

Protein–ligand interactions investigated by thermal shift assays (TSA) and dual polarization interferometry (DPI)

Over the last decades, a wide range of biophysical techniques investigating protein–ligand interactions have become indispensable tools to complement high-resolution crystal structure determinations. Current approaches in solution range from high-throughput-capable methods such as thermal shift assays (TSA) to highly accurate techniques including microscale thermophoresis (MST) and isothermal titration calorimetry (ITC) that can provide a full thermodynamic description of binding events. Surface-based methods such as surface plasmon resonance (SPR) and dual polarization interferometry (DPI) allow real-time measurements and can provide kinetic parameters as well as binding constants. DPI provides additional spatial information about the binding event. Here, an account is presented of new developments and recent applications of TSA and DPI connected to crystallography