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首页> 外文期刊>Analytica chimica acta >Desalting of phosphopeptides by tandem polypyrrole-c18 reverse phase micropipette tip (TMTip_(PPY-c18)) based on hybrid electrostatic, 11-11 stacking and hydrophobic interactions for mass spectrometric analysis
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Desalting of phosphopeptides by tandem polypyrrole-c18 reverse phase micropipette tip (TMTip_(PPY-c18)) based on hybrid electrostatic, 11-11 stacking and hydrophobic interactions for mass spectrometric analysis

机译:基于串联静电,11-11堆积和疏水相互作用的串联聚吡咯-c18反相微量移液器吸头(TMTip_(PPY-c18))对磷酸肽进行脱盐,以进行质谱分析

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摘要

Desalting and concentration of peptides using reverse phase (RP) C18 chromatographic material based on hydrophobic interaction is a routine approach used in mass spectrometry (MS)-based proteomics. However, MS detection of small hydrophiiic peptides, in particular, phosphopeptides that bear multiple negative charges, is challenging due to the insufficient binding to C18 stationary phase. We described here the development of a new desalting method that takes the unique properties of polypyrrole (PPY). The presence of positively charged nitrogen atoms under acidic conditions and polyunsaturated bonds in polypyrrole provide a prospect for enhanced adsorption of phosphopeptides or hydrophiiic peptides through extra electrostatic and Π-Π stacking interactions in addition to hydrophobic interactions. In tandem with reversed phase C18 chromatographic material, the new type of desalting method termed as TMTip_(PPY-C18) can significantly improve the MS detection of phosphopeptides with multiple phosphate groups and other small hydrophiiic peptides. It has been applied to not only tryptic digest of model proteins but also the analysis of complex lysates of zebrafish eggs. The number of detected phosphate groups on a peptide ranged from 1 to 6. Particularly, polypyrrole based method can also be used in basic condition. Thus it provides a useful means to handle peptides that may not be detectable in acidic condition. It can be envisioned that the TMTip_(PPY-C18) should be able to facilitate the exploration of large scale phosphoproteome.
机译:使用基于疏水相互作用的反相(RP)C18色谱材料对肽进行脱盐和浓缩是基于质谱(MS)的蛋白质组学中的常规方法。但是,由于对C18固定相的结合不足,因此对小疏水肽,尤其是带有多个负电荷的磷酸肽的MS检测非常具有挑战性。我们在这里描述了一种采用聚吡咯(PPY)独特性能的新型脱盐方法的开发。在酸性条件下带正电荷的氮原子和聚吡咯中的多不饱和键的存在提供了通过疏水性相互作用以及额外的静电和π-Π堆叠相互作用增强磷酸肽或疏水肽吸附的前景。与反相C18色谱材料配合使用,称为TMTip_(PPY-C18)的新型脱盐方法可以显着改善具有多个磷酸基团和其他小疏水肽的磷酸肽的MS检测。它不仅用于模型蛋白的胰蛋白酶消化,而且还用于斑马鱼卵的复杂裂解物的分析。肽上检测到的磷酸基团的数量为1至6。特别是,在基本条件下也可以使用基于聚吡咯的方法。因此,它提供了一种有用的手段来处理在酸性条件下不可检测的肽。可以预见,TMTip_(PPY-C18)应该能够促进大规模磷酸化蛋白质组的探索。

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