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DOI 10.1021/acs.analchem.5c02002

Медицинская библиотека · Analytical chemistry · 2025

An Integrated Strategy Using Predicted Spectral Library and Tandem Enrichment for Large-Scale Identification of Low-Abundance Proteins and Intact N-Glycopeptides in Human Plasma.

Yang Xinyi, Du Zhuokun, Jiao Yuxin, Chen Sijie, Ning Juanjuan, Hong Haotian, Fu Bin, Liu Jiayu, Zhang Wanjun, Qin Weijie

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

Plasma represents a highly valuable clinical sample for protein biomarker discovery, offering a comprehensive source of physiological and pathological information. N-glycosylation plays key roles in various biological processes and enhances the sensitivity of plasma protein biomarkers for disease diagnosis. Consequently, large-scale characterization of the plasma proteome and N-glycosylation patterns by mass spectrometry (MS) is crucial for identifying biomarkers but remains highly challenging due to three major difficulties. First, plasma protein detection is limited as high-abundance proteins dominate the majority of the MS scans. Second, while plasma proteome coverage can be improved by constructing large-scale empirical spectral libraries and coupling them with DIA-MS, the labor- and time-consuming nature of experimental library generation imposes constraints on its wide adoption in clinical studies. Third, the low concentration and poor ionization of N-glycopeptides make their signals more susceptible to suppression in MS analysis. To address these issues, we developed an integrated workflow applying magnetic graphene-oxide (mGO) nanomaterial enrichment and an in silico predicted spectral library for low-abundance plasma proteome identification, along with tandem enrichment using hydrophilic interaction liquid chromatography (HILIC) for sensitive plasma N-glycoproteome profiling. In this way, 4538 plasma proteins were obtained in a single DIA-MS analysis using a QE-HF mass spectrometer, 10 times more than those obtained from direct analysis of neat plasma. Further HILIC enrichment of the mGO products enabled the identification of 7986 intact N-glycopeptides from 626 proteins with concentrations as low as the nanogram per liter range. Notably, 58.34% of these N-glycopeptides were undetectable by direct HILIC enrichment from neat plasma, highlighting the advantage of applying tandem enrichment.

Для цитирования: Yang Xinyi, Du Zhuokun, Jiao Yuxin, Chen Sijie, Ning Juanjuan, Hong Haotian, Fu Bin, Liu Jiayu, Zhang Wanjun, Qin Weijie. An Integrated Strategy Using Predicted Spectral Library and Tandem Enrichment for Large-Scale Identification of Low-Abundance Proteins and Intact N-Glycopeptides in Human Plasma.. Analytical chemistry. 2025. DOI: 10.1021/acs.analchem.5c02002.

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