磷酸肽
磷酸蛋白质组学
蛋白质组学
蛋白质组
质谱法
细胞培养中氨基酸的稳定同位素标记
定量蛋白质组学
化学
肽
计算生物学
生物
磷酸化
生物化学
蛋白质磷酸化
色谱法
蛋白激酶A
基因
作者
Alexis Chang,Mario Leutert,Ricard A. Rodriguez‐Mias,Judit Villén
标识
DOI:10.1021/acs.jproteome.2c00850
摘要
Phosphotyrosine (pY) enrichment is critical for expanding the fundamental and clinical understanding of cellular signaling by mass spectrometry-based proteomics. However, current pY enrichment methods exhibit a high cost per sample and limited reproducibility due to expensive affinity reagents and manual processing. We present rapid-robotic phosphotyrosine proteomics (R2-pY), which uses a magnetic particle processor and pY superbinders or antibodies. R2-pY can handle up to 96 samples in parallel, requires 2 days to go from cell lysate to mass spectrometry injections, and results in global proteomic, phosphoproteomic, and tyrosine-specific phosphoproteomic samples. We benchmark the method on HeLa cells stimulated with pervanadate and serum and report over 4000 unique pY sites from 1 mg of peptide input, strong reproducibility between replicates, and phosphopeptide enrichment efficiencies above 99%. R2-pY extends our previously reported R2-P2 proteomic and global phosphoproteomic sample preparation framework, opening the door to large-scale studies of pY signaling in concert with global proteome and phosphoproteome profiling.
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