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首页> 外文期刊>Electrophoresis: The Official Journal of the International Electrophoresis Society >Sequence-specific predictive chromatography to assist mass spectrometric analysis of asparagine deamidation and aspartate isomerization in peptides.
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Sequence-specific predictive chromatography to assist mass spectrometric analysis of asparagine deamidation and aspartate isomerization in peptides.

机译:序列特异性预测色谱法可帮助质谱分析肽中的天冬酰胺脱酰胺和天冬氨酸异构化。

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摘要

Deamidation of asparagine and spontaneous isomerization of aspartic acid in proteins and peptides occur frequently. These modifications result in a mixture of peptide variants containing all three residues in the sequences. Identification and isomer quantification for these systems are challenging tasks for tandem mass spectrometry commonly utilized in protein analysis. Chromatographic data provide a set of sequence-specific information complementary to mass spectrometry. In order to compare measured retention times (RTs) with those calculated from the sequences derived from protein databases, it is necessary to develop chromatographic models and tools allowing the prediction of RT and elution order for peptides with modified residues. In this work we extended recently introduced critical liquid chromatography of biomacromolecule model for prediction of RTs for peptides containing asparagines, aspartic acid, and isoaspartic acid residues.
机译:天冬酰胺的脱酰胺作用和天冬氨酸在蛋白质和肽中的自发异构化经常发生。这些修饰导致在序列中包含所有三个残基的肽变体的混合物。对于蛋白质分析中通常使用的串联质谱,这些系统的鉴定和异构体定量分析是具有挑战性的任务。色谱数据提供了一组与质谱互补的序列特定信息。为了将测得的保留时间(RTs)与从蛋白质数据库得出的序列计算出的保留时间(RTs)进行比较,有必要开发色谱模型和工具,以预测具有修饰残基的肽段的RT和洗脱顺序。在这项工作中,我们扩展了最近引入的生物大分子模型的关键液相色谱法,用于预测含有天冬酰胺,天冬氨酸和异天冬氨酸残基的肽的RT。

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