| Literature DB >> 35019217 |
Rania Harrabi1, Thomas Halbritter2, Fabien Aussenac3, Ons Dakhlaoui1,4, Johan van Tol5, Krishna K Damodaran2, Daniel Lee1, Subhradip Paul1, Sabine Hediger1, Frederic Mentink-Vigier5, Snorri Th Sigurdsson2, Gaël De Paëpe1.
Abstract
Efficiently hyperpolarizing proton-dense molecular solids through dynamic nuclear polarization (DNP) solid-state NMR is still an unmet challenge. Polarizing agents (PAs) developed so far do not perform well on proton-rich systems, such as organic microcrystals and biomolecular assemblies. Herein we introduce a new PA, cAsymPol-POK, and report outstanding hyperpolarization efficiency on 12.76 kDa U-13 C,15 N-labeled LecA protein and pharmaceutical drugs at high magnetic fields (up to 18.8 T) and fast magic angle spinning (MAS) frequencies (up to 40 kHz). The performance of cAsymPol-POK is rationalized by MAS-DNP simulations combined with electron paramagnetic resonance (EPR), density functional theory (DFT) and molecular dynamics (MD). This work shows that this new biradical is compatible with challenging biomolecular applications and unlocks the rapid acquisition of 13 C-13 C and 15 N-13 C correlations of pharmaceutical drugs at natural isotopic abundance, which are key experiments for structure determination.Entities:
Keywords: Biomolecules; Dynamic Nuclear Polarization; MAS-DNP; Nuclear Magnetic Resonance; Pharmaceuticals; Polarizing Agents
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Year: 2022 PMID: 35019217 PMCID: PMC8901535 DOI: 10.1002/anie.202114103
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336