Supramolecular Assays for Mapping Enzyme Activity by Displacement‐Triggered Change in Hyperpolarized 129Xe Magnetization Transfer NMR Spectroscopy |
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Authors: | Dr. Matthias Schnurr Dipl.‐Chem. Jagoda Sloniec‐Myszk Dr. Jörg Döpfert Dr. Leif Schröder Dr. Andreas Hennig |
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Affiliation: | 1. ERC Project BiosensorImaging, Leibniz‐Institut für Molekulare Pharmakologie (FMP), Campus BerlinBuch, Robert‐R?ssle‐Strasse 10, 13125 Berlin (Germany);2. BAM Bundesanstalt für Materialforschung und ‐prüfung, Richard‐Willst?tter‐Strasse 11, 12489 Berlin (Germany);3. Department of Life Sciences and Chemistry, Jacobs University Bremen, Campus Ring 1, 28759 Bremen (Germany) |
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Abstract: | Reversibly bound Xe is a sensitive NMR and MRI reporter with its resonance frequency being influenced by the chemical environment of the host. Molecular imaging of enzyme activity presents a promising approach for disease identification, but current Xe biosensing concepts are limited since substrate conversion typically has little impact on the chemical shift of Xe inside tailored cavities. Herein, we exploit the ability of the product of the enzymatic reaction to bind itself to the macrocyclic hosts CB6 and CB7 and thereby displace Xe. We demonstrate the suitability of this method to map areas of enzyme activity through changes in magnetization transfer with hyperpolarized Xe under different saturation scenarios. |
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Keywords: | cucurbituril enzymes NMR spectroscopy supramolecular assays xenon MRI |
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