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Quantification of Proteins by Measuring the Sulfur Content of Their Constituent Peptides by Means of Nano HPLC-ICPMS

机译:通过纳米HPLC-ICPMS测量蛋白质组成肽的硫含量来定量蛋白质

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The sulfur (S) concentrations of three peptides were determined by using nano HPLC-ICPMS under a flow of O_(2) in an octapole reaction cell, and the determined values showed a good agreement with theoretical values. This method was then applied to trypsin-digested peptides from human albumin for protein quantification. Assigning of the number of S atoms in each peptide/peak and the tryptic digestion efficiency were important for protein quantification. The number of S atoms in each peptide/peak was assigned by using verification scores that gave the lowest standard deviation of the peptide S concentration and the highest S recovery. The peptide concentrations were calculated as the ratio of the S concentration/the number of S atoms in the peptide/peak. The tryptic digestion efficiency was calculated as the sum of the S concentration in the mono-peptides divided by the total S concentration in a native polyacrylamide gel electrophoresis (PAGE) band before tryptic digestion. Our result indicates that a protein can be quantified through peptide quantification, after taking into account the tryptic digestion efficiency, via S quantification using ICPMS.
机译:在八极反应池中,通过纳米HPLC-ICPMS在O_(2)流动下,使用三种HPLC测定了三种肽的硫(S)浓度,测定值与理论值吻合良好。然后将该方法应用于人白蛋白中胰蛋白酶消化的肽,以进行蛋白质定量。分配每个肽/峰中的S原子数和胰蛋白酶消化效率对蛋白质定量很重要。通过使用验证分数分配每个肽/峰中的S原子数,这些分数给出了肽S浓度的最低标准偏差和最高的S回收率。肽浓度以S浓度/肽/峰中S原子数之比计算。胰蛋白酶消化效率的计算方法是:将单肽中的S浓度之和除以天然聚丙烯酰胺凝胶电泳(PAGE)谱带中的总S浓度。我们的结果表明,考虑到胰蛋白酶的消化效率,可以通过使用ICPMS的S定量,通过肽定量来定量蛋白质。

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