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

• Published in: Chemical science (Cambridge) Vol. 8; no. 6; pp. 4306 - 4311
• Main Authors: Chen, Bifan, Hwang, Leekyoung, Ochowicz, William, Lin, Ziqing, Guardado-Alvarez, Tania M, Cai, Wenxuan, Xiu, Lichen, Dani, Kunal, Colah, Cyrus, Jin, Song, Ge, Ying
• Format: Journal Article
• Language: English
• Published: England 01-06-2017
• Subjects: Cobalt ferrites; Coupling; Enrichment; Liquid chromatography; Nanoparticles; Phosphorylation; Proteins; Strategy
• ISSN: 2041-6520; 2041-6539
• DOI: 10.1039/c6sc05435h

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 (CoFe
O
) nanoparticles (NPs), and have further developed a top-down phosphoproteomics strategy coupling phosphoprotein enrichment enabled by the functionalized CoFe
O
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.