Qin Zhang-Na, Yu Qiong-Wei, Zhou Ping, Feng Yu-Qi
Department of Chemistry, Wuhan University, Wuhan, 430072, PR China.
Department of Chemistry, Wuhan University, Wuhan, 430072, PR China; Frontier Science Center for Immunology and Metabolism, Wuhan University, Wuhan, 430072, PR China.
Talanta. 2021 Mar 1;224:121790. doi: 10.1016/j.talanta.2020.121790. Epub 2020 Oct 28.
Bioactive polyamines play important roles in many biological processes such as gene expression, cell growth, protein synthesis, and signal transduction. Accurate determination of polyamines is helpful for studying their biological functions. Herein, a C-based chemical labeling strategy was proposed for the determination of polyamines (putrescine, cadaverine, spermidine, and spermine) in biological samples using matrix-assisted laser desorption/ionization mass spectrometry (MALDI MS). An N-hydroxysuccinimide ester functionalized C (NHS-C) was used as a labeling reagent and the m/z of the labeled polyamines reached up to more than 900 Da, which avoided matrix interferences in the low m/z region. In addition, as NHS-C derivatives, mono- and bis-substituted polyamines were produced simultaneously, which benefited the qualitative analysis of polyamines. The analytical method was validated using NHS-C labeled polyamines in cells and mice feces samples. Good linearities were obtained with correlation coefficients ranging from 0.9786 to 0.9982. The limits of quantification were in the range of 0.68-1.48 pmol. Good reproducibility and reliability of our proposed method were confirmed by intra- and inter-day precisions ranged from 2.8 to 16.6%, and the recoveries ranged between 81.8 and 119.9%. Finally, the proposed method was applied to determine polyamines in cells and mice feces. Three polyamines were detected in the cells, and the contents of cadaverine and spermidine in the feces of high-fat diet mice were found to be significantly lower than those in the normal diet mice. The results show that the proposed NHS-C labeling coupled with MALDI MS strategy is suitable for the determination of polyamines in biological samples.
生物活性多胺在许多生物过程中发挥着重要作用,如基因表达、细胞生长、蛋白质合成和信号转导。准确测定多胺有助于研究其生物学功能。在此,提出了一种基于碳的化学标记策略,用于使用基质辅助激光解吸/电离质谱(MALDI MS)测定生物样品中的多胺(腐胺、尸胺、亚精胺和精胺)。一种N-羟基琥珀酰亚胺酯功能化的碳(NHS-C)用作标记试剂,标记后的多胺的质荷比高达900 Da以上,避免了低质荷比区域的基质干扰。此外,作为NHS-C衍生物,单取代和双取代多胺同时产生,这有利于多胺的定性分析。使用NHS-C标记的多胺在细胞和小鼠粪便样品中对该分析方法进行了验证。获得了良好的线性关系,相关系数范围为0.9786至0.9982。定量限在0.68 - 1.48 pmol范围内。通过日内和日间精密度范围为2.8%至16.6%以及回收率范围为81.8%至119.9%,证实了我们提出的方法具有良好的重现性和可靠性。最后,将所提出的方法应用于测定细胞和小鼠粪便中的多胺。在细胞中检测到三种多胺,发现高脂饮食小鼠粪便中尸胺和亚精胺的含量显著低于正常饮食小鼠。结果表明,所提出的NHS-C标记结合MALDI MS策略适用于生物样品中多胺的测定。