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集成单尖端IMAC-HILIC实现植物磷酸蛋白质组学和N-糖蛋白质组学的同步分析。

Integrated Single-Tip IMAC-HILIC Enables Simultaneous Analysis of Plant Phosphoproteomics and N-Glycoproteomics.

作者信息

Chen Chin-Wen, Chen Ting-An, Lin Pei-Yi, Lin Shu-Yu, Hsu Chuan-Chih

机构信息

Institution of Plant and Microbial Biology, Academia Sinica, Taipei 115201, Taiwan.

Academia Sinica Common Mass Spectrometry Facilities for Proteomics and Protein Modification Analysis, Academia Sinica, Taipei 115201, Taiwan.

出版信息

J Proteome Res. 2025 Jul 4;24(7):3560-3568. doi: 10.1021/acs.jproteome.5c00185. Epub 2025 Jun 23.

DOI:10.1021/acs.jproteome.5c00185
PMID:40548449
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12235695/
Abstract

Protein phosphorylation and N-glycosylation are key post-translational modifications (PTMs) in plants that regulate critical signaling processes. However, coanalysis of these PTMs is often complicated by their relatively low abundance and divergent enrichment requirements. Here, we present a single-tip IMAC-HILIC approach that integrates immobilized metal affinity chromatography (IMAC) and hydrophilic interaction chromatography (HILIC) materials within one pipet tip, enabling concurrent enrichment and sequential elution of phosphopeptides and N-glycopeptides. This integrated workflow effectively reduces phosphopeptide coelution during N-glycopeptide elution and streamlines sample processing. In direct comparison with the tandem-tip TIMAHAC method, our single-tip strategy achieves a comparable identification depth and offers superior quantitative accuracy for N-glycopeptides. We further demonstrate its applicability by examining the impact of calcium deprivation in , revealing distinct global changes in both the phosphoproteome and N-glycoproteome. Our optimized protocol thus provides a straightforward and high-throughput platform for dual PTM profiling in complex plant samples, paving the way for broader investigations of PTM crosstalk in diverse physiological and stress responses.

摘要

蛋白质磷酸化和N-糖基化是植物中关键的翻译后修饰(PTM),可调节关键的信号传导过程。然而,由于这些PTM的丰度相对较低且富集要求不同,对它们进行共分析往往很复杂。在这里,我们提出了一种单尖端IMAC-HILIC方法,该方法将固定化金属亲和色谱(IMAC)和亲水相互作用色谱(HILIC)材料整合在一个移液器尖端内,能够同时富集和顺序洗脱磷酸肽和N-糖肽。这种集成的工作流程有效地减少了N-糖肽洗脱过程中磷酸肽的共洗脱,并简化了样品处理。与串联尖端TIMAHAC方法直接比较,我们的单尖端策略实现了相当的鉴定深度,并为N-糖肽提供了更高的定量准确性。我们通过研究钙缺乏对[具体植物名称未给出]的影响进一步证明了其适用性,揭示了磷酸蛋白质组和N-糖蛋白质组中明显的全局变化。因此,我们优化的方案为复杂植物样品中的双重PTM分析提供了一个简单且高通量的平台,并为更广泛地研究不同生理和应激反应中的PTM串扰铺平了道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a063/12235695/148e8add9358/pr5c00185_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a063/12235695/5e6ad9d7df4a/pr5c00185_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a063/12235695/38ab0cf01cfb/pr5c00185_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a063/12235695/c2e4e0601d34/pr5c00185_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a063/12235695/261ec5607c76/pr5c00185_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a063/12235695/66ca3cd06284/pr5c00185_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a063/12235695/148e8add9358/pr5c00185_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a063/12235695/5e6ad9d7df4a/pr5c00185_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a063/12235695/38ab0cf01cfb/pr5c00185_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a063/12235695/c2e4e0601d34/pr5c00185_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a063/12235695/261ec5607c76/pr5c00185_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a063/12235695/66ca3cd06284/pr5c00185_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a063/12235695/148e8add9358/pr5c00185_0006.jpg

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全球磷酸化蛋白质组学分析的进展:克服灵敏度和定量方面的挑战
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