Activatable MRI probes for the specific detection of bacteria.

Prabu Periyathambi, Alien Balian, Zhangjun Hu, Daniel Padro, Luiza I Hernandez, Kajsa Uvdal, Joao Duarte, Frank J Hernandez

Journal: Analytical and bioanalytical chemistry 2022;413(30):7353-7362

PMID: 34704109

Abstract

Activatable fluorescent probes have been successfully used as molecular tools for biomedical research in the last decades. Fluorescent probes allow the detection of molecular events, providing an extraordinary platform for protein and cellular research. Nevertheless, most of the fluorescent probes reported are susceptible to interferences from endogenous fluorescence (background signal) and limited tissue penetration is expected. These drawbacks prevent the use of fluorescent tracers in the clinical setting. To overcome the limitation of fluorescent probes, we and others have developed activatable magnetic resonance probes. Herein, we report for the first time, an oligonucleotide-based probe with the capability to detect bacteria using magnetic resonance imaging (MRI). The activatable MRI probe consists of a specific oligonucleotide that targets micrococcal nuclease (MN), a nuclease derived from Staphylococcus aureus. The oligonucleotide is flanked by a superparamagnetic iron oxide nanoparticle (SPION) at one end, and by a dendron functionalized with several gadolinium complexes as enhancers, at the other end. Therefore, only upon recognition of the MRI probe by the specific bacteria is the probe activated and the MRI signal can be detected. This approach may be widely applied to detect bacterial infections or other human conditions with the potential to be translated into the clinic as an activatable contrast agent.

© 2021. The Author(s).

Address: Department of Physics, Chemistry and Biology, Linkӧping University, 58185, Linköping, Sweden.; Wallenberg Centre for Molecular Medicine, Linköping University, Linköping, Sweden.; Center for Cooperative Research in Biomaterials (CIC biomaGUNE), Basque Research and Technology Alliance (BRTA), 20014, Donostia-San Sebastián, Spain.; Department of Clinical and Experimental Medicine, Linkӧping University, Linköping, Sweden.; Department of Experimental Medical Science, Faculty of Medicine, Lund University, 22181, Lund, Sweden.; Wallenberg Center for Molecular Medicine, Lund University, Lund, Sweden.; Department of Physics, Chemistry and Biology, Linkӧping University, 58185, Linköping, Sweden. [email protected].; Wallenberg Centre for Molecular Medicine, Linköping University, Linköping, Sweden. [email protected].
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