Simultaneous quantification of malonyl-CoA and several other short-chain acyl-CoAs in animal tissues by ion-pairing reversed-phase HPLC/MS

被引:81
作者
Gao, Lan
Chiou, William
Tang, Hua
Cheng, Xueheng
Camp, Heidi S.
Burns, David J.
机构
[1] Abbott Labs, Dept Biol Screening Global Pharmaceut Res & Dev, Abbott Pk, IL 60064 USA
[2] Abbott Labs, Dept Metab Dis Res Global Pharmaceut Res & Dev, Abbott Pk, IL 60064 USA
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2007年 / 853卷 / 1-2期
关键词
coenzyme A (CoA); short-chain acyl-CoA; malonyl-CoA; HPLC; LC/MS; mass spectrometry; beta-oxidation; lipid metabolism; acetyl-CoA; beta-hydroxybutyryl-CoA; succinyl-CoA; 3-hydroxy-3-methylglutaryl-CoA; n-propionyl-CoA; isobutyryl-CoA;
D O I
10.1016/j.jchromb.2007.03.029
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Malonyl-CoA is a key intermediate involved in lipid synthesis and lipid oxidation. Here, we report on a novel method for the quantification of malonyl-CoA and seven other short-chainacyl-CoAs in various rat and mouse tissues using ion-pairing reversed-phase HPLC/MS. This method is capable of measuring malonyl-CoA, free coenzyme A (CoASH), acetyl-CoA, beta-hydroxyl-butyryi-CoA (HB-CoA), 3-hydroxy-3-methyl-glutarylCoA (HMG-CoA), propionyl-CoA, succinyl-CoA, and isobutyryl-CoA simultaneously with a dynamic linear range over two orders of magnitude in a 7.0 min HPLC gradient run. The lower limit of quantification (LLOQ) was 0.225 pmol for all acyl-CoAs studied, except for HMG-CoA which had a higher LLOQ of 0.90 pmol. The interference of HB-CoA on the quantification of malonyl-CoA in animal tissues was also explored for the first time. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:303 / 313
页数:11
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