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Single-step inline hydroxyapatite enrichment facilitates identification and quantitation of phosphopeptides from mass-limited proteomes with MudPIT

机译:单步式羟基磷灰石富集促进了鉴别和定量来自Mudpit的大规模限制蛋白质蛋白磷酸肽

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摘要

Herein we report the characterization and optimization of single-step inline enrichment of phosphopeptides directly from small amounts of whole cell and tissue lysates (100 – 500 μg) using a hydroxyapatite (HAP) microcolumn and Multidimensional Protein Identification Technology (MudPIT). In comparison to a triplicate HILIC-IMAC phosphopeptide enrichment study, ~80% of the phosphopeptides identified using HAP-MudPIT were unique. Similarly, analysis of the consensus phosphorylation motifs between the two enrichment methods illustrates the complementarity of calcium-and iron-based enrichment methods and the higher sensitivity and selectivity of HAP-MudPIT for acidic motifs. We demonstrate how the identification of more multiply phosphorylated peptides from HAP-MudPIT can be used to quantify phosphorylation cooperativity. Through optimization of HAP-MudPIT on a whole cell lysate we routinely achieved identification and quantification of ca. 1000 phosphopeptides from a ~1 hr enrichment and 12 hr MudPIT analysis on small quantities of material. Finally, we applied this optimized method to identify phosphorylation sites from a mass-limited mouse brain region, the amygdala (200 – 500 μg), identifying up to 4000 phosphopeptides per run.
机译:在此,我们报告了使用羟基磷灰石(HAP)微柱和多维蛋白质识别技术(Mudpit)直接由少量全细胞和组织裂解物(100-500μg)直接从少量全细胞和组织裂解物(100-500μg)的单步联线富集的表征和优化。与三份HILIC-IMAC磷酸富集研究相比,使用HAP-MUDPIT鉴定的〜80%的磷酸肽是独特的。类似地,两种富集方法之间的共有磷酸化基序的分析说明了钙和铁基富集方法的互补性以及Hap-Mudpit对于酸性图案的较高灵敏度和选择性。我们证明了如何使用Hap-Mudpit的鉴定更常见的磷酸化肽来量化磷酸化合作。通过优化整个细胞裂解物上的Hap-Mudpit,我们经常实现了CA的识别和量化。 1000来自〜1小时富集的磷酸肽和12小时少量材料的MUDPIT分析。最后,我们应用了这种优化的方法来鉴定来自群体有限的小鼠脑区,杏仁醛(200 - 500μg)的磷酸化位点,鉴定每次运行最多4000种磷酸肽。

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