Nitroxyl Modified Tobacco Mosaic Virus as a Metal-Free High-Relaxivity MRI and EPR Active Superoxide Sensor

• Main Authors: Dharmarwardana, Madushani, Martins, André F., Chen, Zhuo, Palacios, Philip M., Nowak, Chance M., Welch, Raymond P., Li, Shaobo, Luzuriaga, Michael A., Bleris, Leonidas, Pierce, Brad S., Sherry, A. Dean, Gassensmith, Jeremiah J.
• Format: Other/Unknown Material
• Language: unknown
• Published: American Chemical Society (ACS) 2018
• Subjects: Orca
• Online Access: http://dx.doi.org/10.26434/chemrxiv.6241913.v1; https://chemrxiv.org/engage/api-gateway/chemrxiv/assets/orp/resource/item/60c73df9469df43f99f427c5/original/nitroxyl-modified-tobacco-mosaic-virus-as-a-metal-free-high-relaxivity-mri-and-epr-active-superoxide-sensor.pdf

Superoxide overproduction is known to occur in multiple disease states requiring critical care yet non-invasive detection of superoxide in deep tissue remains a challenge. Herein, we report a metal-free magnetic resonance imaging (MRI) and electron paramagnetic resonance (EPR) active contrast agent prepared by “click conjugating” paramagnetic organic radical contrast agents (ORCAs) to the surface of tobacco mosaic virus (TMV). While ORCAs are known to be reduced in vivo to an MRI/EPR silent state, their oxidation is facilitated specifically by reactive oxygen species—in particular superoxide—and are largely unaffected by peroxides and molecular oxygen. Unfortunately, single molecule ORCAs typically offer weak MRI contrast. In contrast, our data confirm that the macromolecular ORCA-TMV conjugates show marked enhancement for T 1 contrast at low field (<3.0 T), and T 2 contrast at high field (9.4 T). Additionally, we demonstrated that the unique topology of TMV allows for “quenchless fluorescent” bimodal probe for concurrent fluorescence and MRI/EPR imaging, which was made possible by exploiting the unique inner and outer surface of the TMV nanoparticle. Finally, we show TMV-ORCAs do not respond to normal cellular respiration, minimizing the likelihood for background, yet still respond to enzymatically produced superoxide in complicated biological fluids like serum.