Fluorous-assisted metal chelate affinity extraction for nucleotides followed by HILIC-MS/MS analysis
We herein developed a selective method for the determination of nucleotides by fluorous-assisted metal chelate affinity extraction followed by hydrophilic interaction liquid chromatography (HILIC) combined with tandem mass spectrometric (MS/MS) analysis. In this study, the nucleotides were selective...
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Published in | Journal of chromatography. B, Analytical technologies in the biomedical and life sciences Vol. 1074-1075; pp. 86 - 90 |
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Elsevier B.V
01.02.2018
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Abstract | We herein developed a selective method for the determination of nucleotides by fluorous-assisted metal chelate affinity extraction followed by hydrophilic interaction liquid chromatography (HILIC) combined with tandem mass spectrometric (MS/MS) analysis. In this study, the nucleotides were selectively chelated by Fe(III)-immobilized perfluoroalkyliminodiacetic acid, and the resulting chelates were subsequently extracted into a fluorous solvent. The nucleotides present in the fluorous solvent were then back-extracted into a non-fluorous solution, such as a solution of ammonia in aqueous acetonitrile. The resulting non-fluorous solution containing the nucleotides was then directly injected into an amide-type HILIC column using a mixture of acetonitrile and aqueous ammonium bicarbonate as the mobile phase for gradient elution, and the nucleotides were detected using the negative electrospray ionization MS/MS mode. In this method, the extraction recoveries of the nucleotides ranged from 43.2 to 94.7% within a relative standard deviation of 17%. This method enabled the determination of intracellular concentrations of nucleotides.
•A fluorous-assisted metal chelate affinity method was applied to the extraction of nucleotides.•Nucleotides could be selectively extracted to fluorous solvent.•The extracted nucleotides were then analyzed with HILIC-MS/MS.•This method enabled the analysis of intracellular concentrations of nucleotides. |
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AbstractList | We herein developed a selective method for the determination of nucleotides by fluorous-assisted metal chelate affinity extraction followed by hydrophilic interaction liquid chromatography (HILIC) combined with tandem mass spectrometric (MS/MS) analysis. In this study, the nucleotides were selectively chelated by Fe(III)-immobilized perfluoroalkyliminodiacetic acid, and the resulting chelates were subsequently extracted into a fluorous solvent. The nucleotides present in the fluorous solvent were then back-extracted into a non-fluorous solution, such as a solution of ammonia in aqueous acetonitrile. The resulting non-fluorous solution containing the nucleotides was then directly injected into an amide-type HILIC column using a mixture of acetonitrile and aqueous ammonium bicarbonate as the mobile phase for gradient elution, and the nucleotides were detected using the negative electrospray ionization MS/MS mode. In this method, the extraction recoveries of the nucleotides ranged from 43.2 to 94.7% within a relative standard deviation of 17%. This method enabled the determination of intracellular concentrations of nucleotides. We herein developed a selective method for the determination of nucleotides by fluorous-assisted metal chelate affinity extraction followed by hydrophilic interaction liquid chromatography (HILIC) combined with tandem mass spectrometric (MS/MS) analysis. In this study, the nucleotides were selectively chelated by Fe(III)-immobilized perfluoroalkyliminodiacetic acid, and the resulting chelates were subsequently extracted into a fluorous solvent. The nucleotides present in the fluorous solvent were then back-extracted into a non-fluorous solution, such as a solution of ammonia in aqueous acetonitrile. The resulting non-fluorous solution containing the nucleotides was then directly injected into an amide-type HILIC column using a mixture of acetonitrile and aqueous ammonium bicarbonate as the mobile phase for gradient elution, and the nucleotides were detected using the negative electrospray ionization MS/MS mode. In this method, the extraction recoveries of the nucleotides ranged from 43.2 to 94.7% within a relative standard deviation of 17%. This method enabled the determination of intracellular concentrations of nucleotides. •A fluorous-assisted metal chelate affinity method was applied to the extraction of nucleotides.•Nucleotides could be selectively extracted to fluorous solvent.•The extracted nucleotides were then analyzed with HILIC-MS/MS.•This method enabled the analysis of intracellular concentrations of nucleotides. |
Author | Nohta, Hitoshi Kiyokawa, Ena Hayama, Tadashi Yoshida, Hideyuki Yamaguchi, Masatoshi |
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CitedBy_id | crossref_primary_10_1016_j_chroma_2023_464386 crossref_primary_10_1016_j_jpba_2018_08_030 crossref_primary_10_1248_cpb_c22_00453 crossref_primary_10_3390_life11060512 crossref_primary_10_1021_acs_jproteome_2c00736 crossref_primary_10_1039_D0AY01860K crossref_primary_10_1021_acs_analchem_3c01998 crossref_primary_10_1080_10408347_2021_1907173 |
Cites_doi | 10.1016/j.chroma.2011.09.037 10.1016/0378-4347(93)80024-X 10.1016/j.jpba.2014.04.035 10.1126/science.1057567 10.1016/j.jchromb.2010.05.016 10.1016/j.jchromb.2008.07.005 10.1093/glycob/cwq044 10.1016/j.talanta.2016.04.058 10.1016/j.jchromb.2009.09.030 10.1016/j.jchromb.2009.05.027 10.1016/j.ab.2007.03.018 10.1021/ac3020092 10.15583/jpchrom.2015.001 |
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Keywords | Nucleotide Cell sample Fluorous-assisted metal chelate affinity HILIC-MS/MS |
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Title | Fluorous-assisted metal chelate affinity extraction for nucleotides followed by HILIC-MS/MS analysis |
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