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通过微液相色谱-电喷雾串联质谱法分析磷酸肽

Analysis of Phosphopeptides by {micro}LC-ESI-MS/MS.

作者信息

Corthals Garry L, Wasinger Valerie C, Goodlett David R

出版信息

CSH Protoc. 2007 Nov 1;2007:pdb.prot4625. doi: 10.1101/pdb.prot4625.

Abstract

INTRODUCTIONWhether using a pressure cell or gel-loader tips, IMAC-purified peptides can be injected into a μLC separation system and analyzed by μLC-ESI-MS/MS. Phosphopeptides behave and elute similarly to nonphosphorylated peptides during RP-HPLC, but because of a decrease in hydrophobicity due to the addition of the phosphate moiety, a phosphopeptide will generally elute before the nonphosphopeptide with the identical amino acid sequence. This difference in elution time is most pronounced for short peptides. Thus, when analyzing phosphopeptides from μLC online with ESI-MS/MS, it is prudent to acquire data during the wash step (i.e., prior to gradient elution), as some short phosphopeptides may not even bind to the C(18) resin in 100% aqueous solutions. Otherwise, these very hydrophilic peptides will be missed. This protocol provides typical μLC conditions for the separation of IMAC-enriched phosphopeptides when the μLC system is online with the ESI-MS/MS.

摘要

引言

无论是使用压力细胞还是凝胶加样器吸头,通过IMAC纯化的肽段都可以注入微液相色谱(μLC)分离系统,并通过μLC-电喷雾电离串联质谱(μLC-ESI-MS/MS)进行分析。在反相高效液相色谱(RP-HPLC)过程中,磷酸化肽段的行为和洗脱情况与非磷酸化肽段相似,但由于磷酸基团的添加导致疏水性降低,具有相同氨基酸序列的磷酸化肽段通常会比非磷酸化肽段先洗脱。这种洗脱时间的差异在短肽中最为明显。因此,当使用ESI-MS/MS对μLC在线分析的磷酸化肽段进行分析时,在清洗步骤(即梯度洗脱之前)采集数据是明智的,因为一些短的磷酸化肽段在100%水溶液中甚至可能不与C(18)树脂结合。否则,这些非常亲水的肽段将会被遗漏。本方案提供了μLC系统与ESI-MS/MS在线联用分离IMAC富集的磷酸化肽段时的典型μLC条件。

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