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Coupling functionalized cobalt ferrite nanoparticle enrichment with online LC/MS/MS for top-down phosphoproteomics

机译:自上而下的磷酸化蛋白质组学与在线LC / MS / MS耦合功能化钴铁氧体纳米颗粒富集

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摘要

Phosphorylation plays pivotal roles in cellular processes and dysregulated phosphorylation is considered as an underlying mechanism in many human diseases. Top-down mass spectrometry (MS) analyzes intact proteins and provides a comprehensive analysis of protein phosphorylation. However, top-down MS-based phosphoproteomics is challenging due to the difficulty in enriching low abundance intact phosphoproteins as well as separating and detecting the enriched phosphoproteins from complex mixtures. Herein, we have designed and synthesized the next generation functionalized superparamagnetic cobalt ferrite (CoFe2O4) nanoparticles (NPs), and have further developed a top-down phosphoproteomics strategy coupling phosphoprotein enrichment enabled by the functionalized CoFe2O4 NPs with online liquid chromatography (LC)/MS/MS for comprehensive characterization of phosphoproteins. We have demonstrated the highly specific enrichment of a minimal amount of spike-in β-casein from a complex tissue lysate as well as effective separation and quantification of its phosphorylated genetic variants. More importantly, this integrated top-down phosphoproteomics strategy allows for enrichment, identification, quantification, and comprehensive characterization of low abundance endogenous phosphoproteins from complex tissue extracts on a chromatographic time scale.
机译:磷酸化在细胞过程中起关键作用,磷酸化失调被认为是许多人类疾病的潜在机制。自顶向下质谱(MS)分析完整的蛋白质并提供蛋白质磷酸化的全面分析。然而,由于难以富集低丰度完整磷蛋白以及难以从复杂混合物中分离和检测富集的磷蛋白,因此自上而下的基于MS的磷蛋白组学具有挑战性。本文中,我们已经设计并合成了下一代功能化超顺磁性钴铁氧体(CoFe2O4)纳米颗粒(NPs),并进一步开发了一种自上而下的磷酸蛋白质组学策略,结合了功能化CoFe2O4 NPs与在线液相色谱(LC)/ MS结合实现的磷蛋白富集/ MS全面鉴定磷蛋白。我们已经证明了从复杂的组织裂解物中微量掺入β-酪蛋白的高度特异性富集,以及其磷酸化遗传变异的有效分离和定量。更重要的是,这种集成的自上而下的磷酸化蛋白质组学策略可在色谱时间范围内对复杂组织提取物中的低丰度内源性磷蛋白进行富集,鉴定,定量和全面表征。

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