A New Evaluation Metric for Quantitative Accuracy of LC–MS/MS-Based Proteomics with Data-Independent Acquisition

Data-independent acquisition (DIA) has improved the identification and quantitation coverage of peptides and proteins in liquid chromatography–tandem mass spectrometry-based proteomics. However, different DIA data-processing tools can produce very different identification and quantitation results fo...

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Veröffentlicht in:Journal of proteome research 2024-09, Vol.23 (9), p.3780-3790
Hauptverfasser: Shi, Mengtian, Huang, Chiyuan, Chen, Renhui, Chen, David Da Yong, Yan, Binjun
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Sprache:eng
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Zusammenfassung:Data-independent acquisition (DIA) has improved the identification and quantitation coverage of peptides and proteins in liquid chromatography–tandem mass spectrometry-based proteomics. However, different DIA data-processing tools can produce very different identification and quantitation results for the same data set. Currently, benchmarking studies of DIA tools are predominantly focused on comparing the identification results, while the quantitative accuracy of DIA measurements is acknowledged to be important but insufficiently investigated, and the absence of suitable metrics for comparing quantitative accuracy is one of the reasons. A new metric is proposed for the evaluation of quantitative accuracy to avoid the influence of differences in false discovery rate control stringency. The part of the quantitation results with high reliability was acquired from each DIA tool first, and the quantitative accuracy was evaluated by comparing quantification error rates at the same number of accurate ratios. From the results of four benchmark data sets, the proposed metric was shown to be more sensitive to discriminating the quantitative performance of DIA tools. Moreover, the DIA tools with advantages in quantitative accuracy were consistently revealed by this metric. The proposed metric can also help researchers in optimizing algorithms of the same DIA tool and sample preprocessing methods to enhance quantitative accuracy.
ISSN:1535-3893
1535-3907
1535-3907
DOI:10.1021/acs.jproteome.4c00088