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Simultaneous determination of ribonucleoside and deoxyribonucleoside triphosphates in biological samples by hydrophilic interaction liquid chromatography coupled with tandem mass spectrometry
被引:39
|作者:
Kong, Ziqing
[1
]
Jia, Shaodong
[1
]
Chabes, Anna Lena
[1
]
Appelblad, Patrik
[2
,3
]
Lundmark, Richard
[4
,5
]
Moritz, Thomas
[6
]
Chabes, Andrei
[1
,5
]
机构:
[1] Umea Univ, Dept Med Biochem & Biophys, SE-90187 Umea, Sweden
[2] Umea Univ, Dept Pharmacol & Clin Neurosci, SE-90187 Umea, Sweden
[3] Merck Chem & Life Sci AB, SE-16903 Solna, Sweden
[4] Umea Univ, Dept Integrat Med Biol, SE-90187 Umea, Sweden
[5] Umea Univ, Lab Mol Infect Med Sweden MIMS, SE-90187 Umea, Sweden
[6] SLU, Dept Forest Genet & Plant Physiol, Umea Plant Sci Ctr UPSC, SE-90187 Umea, Sweden
基金:
瑞典研究理事会;
关键词:
IMBALANCED DNTP POOLS;
REPLICATION STRESS;
DNA-REPLICATION;
CELL-EXTRACTS;
IN-VIVO;
SEPARATION;
REDUCTASE;
DAMAGE;
QUANTIFICATION;
NUCLEOTIDES;
D O I:
10.1093/nar/gky203
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Information about the intracellular concentration of dNTPs and NTPs is important for studies of the mechanisms of DNA replication and repair, but the low concentration of dNTPs and their chemical similarity to NTPs present a challenge for their measurement. Here, we describe a new rapid and sensitive method utilizing hydrophilic interaction liquid chromatography coupled with tandem mass spectrometry for the simultaneous determination of dNTPs and NTPs in biological samples. The developed method showed linearity (R-2 > 0.99) in wide concentration ranges and could accurately quantify dNTPs and NTPs at low pmol levels. The intra-day and inter-day precision were below 13%, and the relative recovery was between 92% and 108%. In comparison with other chromatographic methods, the current method has shorter analysis times and simpler sample pretreatment steps, and it utilizes an ion-pair-free mobile phase that enhances mass-spectrometric detection. Using this method, we determined dNTP and NTP concentrations in actively dividing and quiescent mouse fibroblasts.
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