多路复用
化学
等压法
蛋白质组
计算生物学
等压标记
色谱法
鉴定(生物学)
无标记量化
定量蛋白质组学
质谱法
蛋白质组学
计算机科学
生物化学
串联质谱法
电信
生物
物理
植物
基因
热力学
蛋白质质谱法
作者
Zhiyong Wu,Xin Huang,Lin Huang,Xumin Zhang
标识
DOI:10.1021/acs.analchem.3c03036
摘要
Hyperplexing approaches have been aimed to meet the demand for large-scale proteomic analyses. Currently, the analysis capacity has expanded to up to 54 samples within a single experiment by utilizing different isotopic and isobaric reagent combinations. In this report, we propose a super multiplexed approach to enable the analysis of up to 102 samples in a single experiment, by the combination of our recently developed TAG-TMTpro and TAG-IBT16 labeling. We systematically investigated the identification and quantification performance of the 102-plex approach using the mixtures of E. coli and HeLa peptides. Our results revealed that all labeling series demonstrated accurate and reliable quantification performance. The combination of TAG-IBT16 and TAG-TMTpro approaches expands the multiplexing capacity to 102 plexes, providing a more multiplexed quantification method for even larger-scale proteomic analysis. Data are available via ProteomeXchange with the identifier PXD042398.
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