首页> 外文OA文献 >Fractionation of Enriched Phosphopeptides Using pH/Acetonitrile-Gradient-Reversed-Phase Microcolumn Separation in Combination with LC–MS/MS Analysis
【2h】

Fractionation of Enriched Phosphopeptides Using pH/Acetonitrile-Gradient-Reversed-Phase Microcolumn Separation in Combination with LC–MS/MS Analysis

机译:使用pH /乙腈 - 梯度反相的相位微柱分离与LC-MS / MS分析组合的富集磷酸肽的分馏

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Mass spectrometry (MS) is a powerful and sensitive method often used for the identification of phosphoproteins. However, in phosphoproteomics, there is an identified need to compensate for the low abundance, insufficient ionization, and suppression effects of non-phosphorylated peptides. These may hamper the subsequent liquid chromatography–mass spectrometry/mass spectrometry (LC–MS/MS) analysis, resulting in incomplete phosphoproteome characterization, even when using high-resolution instruments. To overcome these drawbacks, we present here an effective microgradient chromatographic technique that yields specific fractions of enriched phosphopeptides compatible with LC–MS/MS analysis. The purpose of our study was to increase the number of identified phosphopeptides, and thus, the coverage of the sample phosphoproteome using the reproducible and straightforward fractionation method. This protocol includes a phosphopeptide enrichment step followed by the optimized microgradient fractionation of enriched phosphopeptides and final LC–MS/MS analysis of the obtained fractions. The simple fractionation system consists of a gas-tight microsyringe delivering the optimized gradient mobile phase to reversed-phase microcolumn. Our data indicate that combining the phosphopeptide enrichment with the microgradient separation is a promising technique for in-depth phosphoproteomic analysis due to moderate input material requirements and more than 3-fold enhanced protein identification.
机译:质谱(MS)是一种强大而敏感的方法,通常用于鉴定磷蛋白。然而,在磷蛋白酶中,存在鉴定需要补偿低丰度,不足的电离和非磷酸化肽的抑制作用。这些可能妨碍随后的液相色谱 - 质谱/质谱(LC-MS / MS)分析,导致磷酸溶解组特征不完全,即使在使用高分辨率仪器时也是如此。为了克服这些缺点,我们在此提出了一种有效的微润肤型色谱技术,其产生与LC-MS / MS分析相容的富集的磷酸肽的特异性分数。我们研究的目的是增加鉴定的磷酸肽的数量,从而增加样品磷酸酯组的覆盖,使用可再现和直接的分馏方法。该方案包括磷酸富集富集步骤,然后进行富集的磷酸肽和最终LC-MS / MS分析所获得的级分的优化微血晶分馏。简单的分馏系统包括将优化的梯度流动相输送到反相微柱的气密微倍。我们的数据表明,将磷肽富集与微染色体分离相结合是由于中度输入材料要求和增强蛋白质鉴定超过3倍的蛋白质鉴定的深入磷蛋白酶分析的有希望的技术。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号