Benchtop NMR is becoming an increasingly important tool, sometimes providing a simple and low-cost alternative to high-field NMR. The Achilles heel of NMR and even more critically of benchtop NMR is its limited sensitivity. However, when combined with hyperpolarization techniques, the sensitivity boost can provide excellent sensitivity that can even make benchtop NMR compatible with affinity studies for drug discovery. Hyperpolarization by dissolution dynamic nuclear polarization (dDNP) provides a route to enhancing C nuclear magnetic resonance (NMR) sensitivity by more than 5 orders of magnitude for a wide range of small molecules on a benchtop NMR system. We show here how ligands can be secondarily labeled with C tags and hyperpolarized with conventional dDNP methods. These hyperpolarized ligands display long nuclear spin-lattice relaxation time constants and can therefore be used to probe interactions with target proteins in conventional dDNP settings. The boost in sensitivity combined with the simplicity of the C spectra (one peak per ligand) enables detection on an 80 MHz benchtop NMR spectrometer at micromolar concentrations, which may ultimately provide a way of improving and accelerating the discovery of new drug candidates.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11800164PMC
http://dx.doi.org/10.1021/acsomega.4c05101DOI Listing

Publication Analysis

Top Keywords

benchtop nmr
24
nmr
9
nmr spectrometer
8
hyperpolarized ligands
8
sensitivity combined
8
conventional ddnp
8
benchtop
6
sensitivity
5
micromolar concentration
4
concentration affinity
4

Similar Publications

This Perspective seeks to reconnect the current practice of nuclear magnetic resonance (NMR) spectroscopy in chemical structure and quantitative (qNMR) analysis with its roots in classical physics and quantum mechanics (QM). Rationales for this approach are derived from various angles, including focused reviews of the key parameters of the nuclear resonance phenomenon, the structural information richness of NMR spectra, and significant progress in both computational and spectrometer hardware. This provides collective reasoning for the reintegration of computational quantum mechanical spectral analysis (QMSA) into the contemporary practice of NMR spectral interpretation.

View Article and Find Full Text PDF

Real-time monitoring of fermentation processes in wine production with benchtop H NMR spectroscopy.

Food Res Int

February 2025

Laboratory of Engineering Thermodynamics (LTD), RPTU Kaiserslautern, Erwin-Schrödinger-Straße 44, 67663 Kaiserslautern, Germany; Laboratory of Advanced Spin Engineering - Magnetic Resonance (LASE-MR), RPTU Kaiserslautern, Gottlieb-Daimler-Straße 76, 67663, Kaiserslautern, Germany. Electronic address:

The flexibility, affordability and ease of use of benchtop H NMR spectroscopy makes it potentially very interesting for assessing the quality of wine types and monitoring the fermentation process. However, the low spectral resolution of benchtop H NMR spectroscopy and the complexity of the mixtures hinder the direct quantification of important wine parameters and, thus, prevent its widespread use as an analytical tool in wineries. We show here that these problems can be solved using model-based data processing.

View Article and Find Full Text PDF

Overhauser Dynamic Nuclear Polarization Enables Single Scan Benchtop C NMR Spectroscopy in Continuous-Flow.

Anal Chem

March 2025

Laboratory of Engineering Thermodynamics (LTD), RPTU Kaiserslautern, Erwin-Schrödinger-Straße 44, 67663 Kaiserslautern, Germany.

Benchtop C NMR spectroscopy is highly attractive for reaction and process monitoring. However, insufficient premagnetization and low signal intensities largely prevent its application to flowing liquids. We show that hyperpolarization by Overhauser dynamic nuclear polarization (ODNP) can be used to overcome these problems, as ODNP operates on short time scales and results in strong C signal enhancements.

View Article and Find Full Text PDF

Programmable synthesis of polymer nanoparticles prepared by polymerization-induced self-assembly (PISA) mediated by reversible addition-fragmentation chain-transfer (RAFT) dispersion polymerization with specified diameter is achieved in an automated flow-reactor platform. Real-time particle size and monomer conversion is obtained via inline spatially resolved dynamic light scattering (SRDLS) and benchtop nuclear magnetic resonance (NMR) instrumentation. An initial training experiment generated a relationship between copolymer block length and particle size for the synthesis of poly(,-dimethylacrylamide)--poly(diacetone acrylamide) (PDMAm--PDAAm) nanoparticles.

View Article and Find Full Text PDF

Time-Domain NMR: Generating Unique Insights into the Characterization of Heterogeneous Catalysis in Liquid Phase.

ACS Catal

February 2025

Department of Chemical and Petroleum Engineering, Center for Environmentally Beneficial Catalysis, and Wonderful Institute for Sustainable Engineering, University of Kansas, Lawrence, Kansas 66045, United States.

Time-domain (TD) nuclear magnetic resonance (NMR) comprises a family of tools for characterizing wetted porosity and surface area, fluid-catalyst surface adsorption energy, liquid distribution in packed beds, and transport of fluids in catalyst materials. These methods are differentiated from NMR spectroscopy in that the data are not analyzed in the frequency domain and often benefit from the use of low magnetic field strength. The increased accessibility of commercial, low-field, benchtop NMR instruments has supported substantial growth in TD NMR research in catalysis.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!