TY - JOUR
T1 - Compound-Specific 1D 1H NMR Pulse Sequence Selection for Metabolomics Analyses
AU - Singh, Upendra
AU - Alsuhaymi, Shuruq
AU - Al-Nemi, Ruba
AU - Emwas, Abdul Hamid
AU - Jaremko, Mariusz
N1 - Funding Information:
The authors would like to thank King Abdullah University of Science and Technology (KAUST) for financial support. Smart Health Initiative (SHI) is also acknowledged by M.J. for the grants financed with the source of Baseline (BAS/1/1085-01-01) in the period of 2021–2023.
Publisher Copyright:
© 2023 The Authors. Published by American Chemical Society
PY - 2023/7/4
Y1 - 2023/7/4
N2 - NMR-based metabolomics approaches have been used in a wide range of applications, for example, with medical, plant, and marine samples. One-dimensional (1D) 1H NMR is routinely used to find out biomarkers in biofluids such as urine, blood plasma, and serum. To mimic biological conditions, most NMR studies have been carried out in an aqueous solution where the high intensity of the water peak is a major problem in obtaining a meaningful spectrum. Different methods have been used to suppress the water signal, including 1D Carr-Purcell-Meiboom-Gill (CPMG) presat, consisting of a T2 filter to suppress macromolecule signals and reduce the humped curve in the spectrum. 1D nuclear Overhauser enhancement spectroscopy (NOESY) is another method for water suppression that is used routinely in plant samples with fewer macromolecules than in biofluid samples. Other common 1D 1H NMR methods such as 1D 1H presat and 1D 1H ES have simple pulse sequences; their acquisition parameters can be set easily. The proton with presat has just one pulse and the presat block causes water suppression, while other 1D 1H NMR methods including those mentioned above have more pulses. However, it is not well known in metabolomics studies because it is used only occasionally and in a few types of samples by metabolomics experts. Another effective method is excitation sculpting to suppress water. Herein, we evaluate the effect of method selection on signal intensities of commonly detected metabolites. Different classes of samples including biofluid, plant, and marine samples were investigated, and recommendations on the advantages and limitations of each method are presented.
AB - NMR-based metabolomics approaches have been used in a wide range of applications, for example, with medical, plant, and marine samples. One-dimensional (1D) 1H NMR is routinely used to find out biomarkers in biofluids such as urine, blood plasma, and serum. To mimic biological conditions, most NMR studies have been carried out in an aqueous solution where the high intensity of the water peak is a major problem in obtaining a meaningful spectrum. Different methods have been used to suppress the water signal, including 1D Carr-Purcell-Meiboom-Gill (CPMG) presat, consisting of a T2 filter to suppress macromolecule signals and reduce the humped curve in the spectrum. 1D nuclear Overhauser enhancement spectroscopy (NOESY) is another method for water suppression that is used routinely in plant samples with fewer macromolecules than in biofluid samples. Other common 1D 1H NMR methods such as 1D 1H presat and 1D 1H ES have simple pulse sequences; their acquisition parameters can be set easily. The proton with presat has just one pulse and the presat block causes water suppression, while other 1D 1H NMR methods including those mentioned above have more pulses. However, it is not well known in metabolomics studies because it is used only occasionally and in a few types of samples by metabolomics experts. Another effective method is excitation sculpting to suppress water. Herein, we evaluate the effect of method selection on signal intensities of commonly detected metabolites. Different classes of samples including biofluid, plant, and marine samples were investigated, and recommendations on the advantages and limitations of each method are presented.
UR - http://www.scopus.com/inward/record.url?scp=85164453022&partnerID=8YFLogxK
U2 - 10.1021/acsomega.3c01688
DO - 10.1021/acsomega.3c01688
M3 - Article
C2 - 37426221
AN - SCOPUS:85164453022
SN - 2470-1343
VL - 8
SP - 23651
EP - 23663
JO - ACS OMEGA
JF - ACS OMEGA
IS - 26
ER -