非水缓冲剂对多肽毛细管电泳-质谱分析的影响。

Leesa J Deterding, Morteza Khaledi, Kenneth B Tomer
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引用次数: 0

摘要

以合成多肽为模型化合物,研究了不同浓度的非水改性剂对毛细管电泳的影响。电渗透流在每个二元溶剂系统中进行比较,在所有情况下,有机溶剂浓度的增加导致电渗透流的减少。计算了每个肽的电泳迁移率,在乙腈的情况下,很少或没有观察到肽迁移率的变化。一般来说,随着甲醇和n -甲基甲酰胺浓度的增加,观察到肽的电泳迁移率降低。评估了每种改性剂在25% (vol/vol)时用于质谱检测的相容性。从我们的数据来看,与甲醇和n -甲基甲酰胺相比,在CE缓冲液中添加乙腈似乎与质谱法最相容,因为分析时间更短,灵敏度更高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of nonaqueous buffer modifiers on the capillary electrophoresis-mass spectrometry analysis of peptides.

The effect of the addition of nonaqueous modifiers in capillary electrophoresis at varying concentrations was determined using synthetic peptides as model compounds. The electroosmotic flow is compared in each of the binary solvent systems and, in all cases, an increase in the concentration of organic solvent resulted in a decrease in the electroosmotic flow. The electrophoretic mobilities of each peptide were calculated and, in the case of acetonitrile, little or no change was observed in the peptide mobilities. In general, a decrease in the electrophoretic mobilities of the peptides was observed for increasing concentrations of methanol and N-methylformamide. The compatibility of each modifier at 25% (vol/vol) for use with mass spectrometric detection was evaluated. From our data, the addition of acetonitrile to the CE buffer appears to be the most compatible with mass spectrometry due to shorter analysis times and increased sensitivities in comparison to methanol and N-methylformamide.

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