Hyperpolarization-Enhanced NMR Spectroscopy of Unaltered Biofluids Using Photo-CIDNP

被引:2
|
作者
Kuhn, Lars T. [1 ]
Weber, Stefan [1 ]
Bargon, Joachim [2 ]
Parella, Teodor [3 ]
Perez-Trujillo, Miriam [3 ]
机构
[1] Albert Ludwigs Univ Freiburg, Inst Phys Chem, D-79104 Freiburg, Germany
[2] Rheinische Friedrich Wilhelms Univ Bonn, Inst Phys & Theoret Chem, D-53115 Bonn, Germany
[3] Univ Autonoma Barcelona, Serv Ressonancia Magnet Nucl, Fac Ciencies & Biosci, Cerdanyola Del Valles 08193, Catalonia, Spain
关键词
DYNAMIC NUCLEAR-POLARIZATION; AMINO-ACIDS; ILLUMINATION; TRYPTOPHAN;
D O I
10.1021/acs.analchem.3c03215
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The direct and unambiguous detection and identification of individual metabolite molecules present in complex biological mixtures constitute a major challenge in (bio)-analytical research. In this context, nuclear magnetic resonance (NMR) spectroscopy has proven to be particularly powerful owing to its ability to provide both qualitative and quantitative atomic-level information on multiple analytes simultaneously in a noninvasive manner. Nevertheless, NMR suffers from a low inherent sensitivity and, moreover, lacks selectivity regarding the number of individual analytes to be studied in a mixture of a myriad of structurally and chemically very different molecules, e.g., metabolites in a biofluid. Here, we describe a method that circumvents these shortcomings via performing selective, photochemically induced dynamic nuclear polarization (photo-CIDNP) enhanced NMR spectroscopy on unmodified complex biological mixtures, i.e., human urine and serum, which yields a single, background-free one-dimensional NMR spectrum. In doing this, we demonstrate that photo-CIDNP experiments on unmodified complex mixtures of biological origin are feasible, can be performed straightforwardly in the native aqueous medium at physiological metabolite concentrations, and act as a spectral filter, facilitating the analysis of NMR spectra of complex biofluids. Due to its noninvasive nature, the method is fully compatible with state-of-the-art metabolomic protocols providing direct spectroscopic information on a small, carefully selected subset of clinically relevant metabolites. We anticipate that this approach, which, in addition, can be combined with existing high-throughput/high-sensitivity NMR methodology, holds great promise for further in-depth studies and development for use in metabolomics and many other areas of analytical research.
引用
收藏
页码:102 / 109
页数:8
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