Trehalose matrices for high temperature dynamic nuclear polarization enhanced solid state NMR.


Journal

Physical chemistry chemical physics : PCCP
ISSN: 1463-9084
Titre abrégé: Phys Chem Chem Phys
Pays: England
ID NLM: 100888160

Informations de publication

Date de publication:
25 May 2022
Historique:
pubmed: 12 5 2022
medline: 27 5 2022
entrez: 11 5 2022
Statut: epublish

Résumé

Dynamic nuclear polarization (DNP) at cryogenic temperatures has proved to be a valuable technique to enhance the sensitivity of solid-state NMR spectroscopy. Over the years, sample formulations have been optimized for experiments at cryogenic temperatures. At 9.4 T, the best performing polarizing agents are dinitroxides such as AMUPol and TEKPol that lead to enhancement factors of around 250 at 100 K. However, the performance of these radicals plummets at higher temperatures. Here we introduce trehalose-based DNP polarizing matrices, suitable to embed biomolecular assemblies. Several formulation protocols are investigated, in combination with various polarizing agents, including a new biradical structure chemically tethered to a trehalose molecule. The DNP efficiency of these new polarizing media is screened as a function of the radical concentration, the hydration level of the matrix and the protein content. Sizeable enhancement factors are reported at 100 K and 9.4 T. More importantly, we show that the DNP performance of these new polarizing media outperform the conventionally used water/glycerol mixture at temperatures above 180 K. This study establishes trehalose matrices as a promising DNP medium for experiments at temperatures >150 K where conventional water-based formulations soften and are no longer viable, thus opening new avenues for DNP enhanced solid-state NMR spectroscopy at temperatures close to ambient temperature.

Identifiants

pubmed: 35543564
doi: 10.1039/d2cp00970f
doi:

Substances chimiques

Water 059QF0KO0R
Trehalose B8WCK70T7I

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

12167-12175

Auteurs

Monu Kaushik (M)

Centre de RMN à Très Hauts Champs, Université de Lyon/CNRS/ENS Lyon/UCB Lyon 1, 5 Rue de la Doua, 69100 Villeurbanne, France. anne.lesage@ens-lyon.fr.

Hugo Lingua (H)

Aix Marseille Univ., CNRS, Institut de Chimie Radicalaire UMR 7273, 13013 Marseille, France. olivier.ouari@univ-amu.fr.

Gabriele Stevanato (G)

Institut des Sciences et Ingénierie Chimiques, Ecole Polytechnique Fédérale de Lausanne, Av. F.-A. Forel 2, CH-1015 Lausanne, Switzerland.

Margarita Elokova (M)

Centre de RMN à Très Hauts Champs, Université de Lyon/CNRS/ENS Lyon/UCB Lyon 1, 5 Rue de la Doua, 69100 Villeurbanne, France. anne.lesage@ens-lyon.fr.

Moreno Lelli (M)

Center of Magnetic Resonance (CERM), Department of Chemistry, University of Florence, Via della Lastruccia 3, 50019 Sesto Fiorentino.
Consorzio Interuniversitario Risonanze Magnetiche Metallo Proteine (CIRMMP), Via Luigi Sacconi 6, 50019 Sesto Fiorentino.

Anne Lesage (A)

Centre de RMN à Très Hauts Champs, Université de Lyon/CNRS/ENS Lyon/UCB Lyon 1, 5 Rue de la Doua, 69100 Villeurbanne, France. anne.lesage@ens-lyon.fr.

Olivier Ouari (O)

Aix Marseille Univ., CNRS, Institut de Chimie Radicalaire UMR 7273, 13013 Marseille, France. olivier.ouari@univ-amu.fr.

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Classifications MeSH