Biological Sciences, AstraZeneca R&D, 221 87 Lund, Sweden.
Anal Biochem. 2013 Mar 1;434(1):84-92. doi: 10.1016/j.ab.2012.10.033. Epub 2012 Nov 5.
Mucins are of great interest owing to their involvement in physiological and pathological processes in the airways. A method that allows accurate quantification of such proteins in sputum samples may be helpful for research in this field. A liquid chromatographic selected reaction monitoring (SRM) method was developed for the quantification of two mucins, MUC5AC and MUC5B, in induced sputum samples. Sample preparation for the assay included solubilization, reduction, and alkylation prior to tryptic digestion. Solid phase extraction using C18 sorbent was used for sample cleanup prior to the liquid chromatography-tandem mass spectrometry (LC-MS/MS) analysis. A cysteine-containing peptide was selected for quantification of MUC5AC protein, whereas a non-cysteine peptide was used for the quantification of MUC5B protein. Stable isotope-labeled synthetic peptides were used as internal standards, and linear calibration curves were constructed in the range of 0.3 to 40 pmol/L. Both mucins could be determined with a precision of 6 to 19% and an accuracy of 98 to 114%. The method is transferable to robotics and is suitable to be run in a 96-well format.
黏蛋白因其参与气道的生理和病理过程而备受关注。一种能够准确定量痰液样本中此类蛋白质的方法,可能有助于该领域的研究。本研究建立了一种液相色谱-选择反应监测(SRM)方法,用于定量检测诱导痰样本中的两种黏蛋白(MUC5AC 和 MUC5B)。该测定法的样品制备包括溶解、还原和烷基化,然后进行胰蛋白酶消化。在液相色谱-串联质谱(LC-MS/MS)分析之前,采用 C18 吸附剂进行固相萃取以进行样品净化。选择含有半胱氨酸的肽段用于 MUC5AC 蛋白的定量,而非半胱氨酸肽段用于 MUC5B 蛋白的定量。使用稳定同位素标记的合成肽作为内标,在 0.3 至 40 pmol/L 的范围内构建线性校准曲线。两种黏蛋白的精密度为 6%至 19%,准确度为 98%至 114%。该方法可转移至机器人操作,并适合以 96 孔格式运行。