DIA-MS2pep:从数据无关的采集数据中进行全面肽鉴定的无库框架。

Junjie Hou, Jifeng Wang, Fuquan Yang, Tao Xu
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引用次数: 0

摘要

由于高度复用的质谱/质谱,直接从数据独立采集(DIA)数据中识别肽仍然具有挑战性。基于谱库的多肽检测灵敏度高,但受限于谱库的深度,抑制了对DIA数据的发现潜力。我们在这里提出DIA- ms2pep,一个从DIA数据中进行全面肽鉴定的无库框架。DIA-MS2pep采用数据驱动算法,使用碎片数据进行MS/MS频谱解复用,而不需要前体。DIA-MS2pep通过对前体质量耐受数据库的搜索,可以识别出肽及其修饰形式。我们通过将DIA- ms2pep与传统的无文库工具进行比较,证明了DIA- ms2pep在肽鉴定的准确性和敏感性方面的性能,这些工具使用了公开的DIA数据集,包括HeLa细胞裂解物、磷酸肽、血浆等。与基于数据依赖获取的光谱库相比,使用DIA- ms2pep直接从DIA数据构建的光谱库提高了定量蛋白质组的准确性和可重复性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

DIA-MS2pep: a library-free framework for comprehensive peptide identification from data-independent acquisition data.

DIA-MS2pep: a library-free framework for comprehensive peptide identification from data-independent acquisition data.

DIA-MS2pep: a library-free framework for comprehensive peptide identification from data-independent acquisition data.

DIA-MS2pep: a library-free framework for comprehensive peptide identification from data-independent acquisition data.

Identifying peptides directly from data-independent acquisition (DIA) data remains challenging due to the highly multiplexed MS/MS spectra. Spectral library-based peptide detection is sensitive, but it is limited to the depth of the library and mutes the discovery potential of DIA data. We present here, DIA-MS2pep, a library-free framework for comprehensive peptide identification from DIA data. DIA-MS2pep uses a data-driven algorithm for MS/MS spectrum demultiplexing using the fragments data without the need of a precursor. With a large precursor mass tolerance database search, DIA-MS2pep can identify the peptides and their modified forms. We demonstrate the performance of DIA-MS2pep by comparing it to conventional library-free tools in accuracy and sensitivity of peptide identifications using publicly available DIA datasets of varying samples, including HeLa cell lysates, phosphopeptides, plasma, etc. Compared with data-dependent acquisition-based spectral libraries, spectral libraries built directly from DIA data with DIA-MS2pep improve the accuracy and reproducibility of the quantitative proteome.

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CiteScore
1.30
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