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首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Optimization and application of microwave-assisted acid hydrolysis for rapid quantification of protein oxidation markers using LC-MS
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Optimization and application of microwave-assisted acid hydrolysis for rapid quantification of protein oxidation markers using LC-MS

机译:微波辅助酸水解的LC-MS快速定量蛋白质氧化标记物的优化及应用

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Simple and efficient microwave-assisted acid hydrolysis (MAAH) of proteins was used for rapid quantification of α-aminoadipic semialdehyde (AAS) and γ-glutamic semialdehyde (GGS) as major protein oxidation markers. The precursor amino acid residues corresponding to AAS and GGS in oxidized proteins were derivatized by reductive amination with sodium cyanoborohydride (NaCNBH_3) and p-aminobenzoic acid (ABA) followed by MAAH to generate the marker derivatives AAS-ABA and GGS-ABA. The quantification was performed using electrospray ionization liquid chromatography-mass spectrometry (ESI LC-MS). The important parameters for hydrolysis were optimized, which include the temperature, the reaction time, the acid concentration and volume as well as the microwave power. Compared to the conventional acid hydrolysis of 18-24 h using 6-12 M HCl at 110 °C applied commonly in the literature and also in this work, MAAH of proteins can be completed as fast as in only 2-10 min and, additionally, with a 3-5 times higher yield of the final derivatization products. Furthermore, a better agreement between the ratio of the detected derivatization products and the theoretical yields from the studied protein has also been achieved, which indicates that MAAH may serve as a more reliable method of acid hydrolysis for this purpose than that with conventional thermal heating. The MAAH method is demonstrated to be a time-saving, reproducible and efficient technique for studying AAS and GGS as protein oxidation markers using LC-MS.
机译:简单有效的蛋白质微波辅助酸水解法(MAAH)用于快速定量测定主要蛋白质氧化标记物α-氨基己二半醛(AAS)和γ-谷氨酸半醛(GGS)。通过先用氰基硼氢化钠(NaCNBH_3)和对氨基苯甲酸(ABA)然后用MAAH进行还原胺化,衍生化氧化蛋白质中对应于AAS和GGS的前体氨基酸残基,以生成标记衍生物AAS-ABA和GGS-ABA。使用电喷雾电离液相色谱-质谱(ESI LC-MS)进行定量。优化了水解的重要参数,包括温度,反应时间,酸浓度和体积以及微波功率。与文献中以及在这项工作中通常使用的在110°C下使用6-12 M HCl在18-24 h内进行常规酸水解相比,蛋白质的MAAH可以在2-10 min内快速完成,此外,最终衍生产品的收率要高出3-5倍。此外,在检测到的衍生化产物的比率与所研究蛋白质的理论产率之间也达成了更好的一致性,这表明MAAH可以比常规热加热作为更可靠的酸水解方法。 MAAH方法被证明是一种使用LC-MS研究AAS和GGS作为蛋白质氧化标记的省时,可重现和有效的技术。

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