Real-Time Pure Shift HSQC NMR for Untargeted Metabolomics.
István TimáriCheng WangAlexandar L HansenGilson Costa Dos SantosSung Ok YoonLei Bruschweiler-LiRafael BrüschweilerPublished in: Analytical chemistry (2019)
Sensitivity and resolution are key considerations for NMR applications in general and for metabolomics in particular, where complex mixtures containing hundreds of metabolites over a large range of concentrations are commonly encountered. There is a strong demand for advanced methods that can provide maximal information in the shortest possible time frame. Here, we present the optimization and application of the recently introduced 2D real-time BIRD 1H-13C HSQC experiment for NMR-based metabolomics of aqueous samples at 13C natural abundance. For mouse urine samples, it is demonstrated how this real-time pure shift sensitivity-improved heteronuclear single quantum correlation method provides broadband homonuclear decoupling along the proton detection dimension and thereby significantly improves spectral resolution in regions that are affected by spectral overlap. Moreover, the collapse of the scalar multiplet structure of cross-peaks leads to a sensitivity gain of about 40-50% over a traditional 2D HSQC-SI experiment. The experiment works well over a range of magnetic field strengths and is particularly useful when resonance overlap in crowded regions of the HSQC spectra hampers accurate metabolite identification and quantitation.
Keyphrases
- mass spectrometry
- high resolution
- magnetic resonance
- solid state
- liquid chromatography
- ms ms
- optical coherence tomography
- high performance liquid chromatography
- ionic liquid
- energy transfer
- gas chromatography
- high speed
- single molecule
- molecular dynamics
- magnetic resonance imaging
- computed tomography
- tandem mass spectrometry
- heart rate
- room temperature
- body composition
- gas chromatography mass spectrometry
- label free
- loop mediated isothermal amplification
- wastewater treatment
- sensitive detection