Spectral Library Searching To Identify Cross-Linked Peptides

被引:12
|
作者
Schweppe, Devin K. [1 ]
Chavez, Juan D. [1 ]
Navare, Arti T. [1 ]
Wu, Xia [1 ]
Ruiz, Bianca [1 ]
Eng, Jimmy K. [2 ]
Lam, Henry [3 ]
Bruce, James E. [1 ]
机构
[1] Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA 98195 USA
[2] Univ Washington, Sch Med, Univ Washington Prote Resource, Seattle, WA 98195 USA
[3] Hong Kong Univ Sci & Technol, Dept Chem & Biomol Engn, Kowloon, Hong Kong, Peoples R China
基金
美国国家卫生研究院;
关键词
spectral library; XL-MS; protein cross-linking; PROTEIN-PROTEIN INTERACTIONS; LINKING MASS-SPECTROMETRY; INTERACTION NETWORK; IDENTIFICATION; COMPLEX; RESOURCE; REVEALS; CELLS;
D O I
10.1021/acs.jproteome.6b00014
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Methods harnessing protein cross-linking and mass spectrometry (XL-MS) offer high-throughput means to identify protein protein interactions (PPIs) and structural interfaces of protein complexes. Yet, specialized data dependent methods and search algorithms are often required to confidently assign peptide identifications to spectra. To improve the efficiency of matching high confidence spectra, we developed a spectral library based approach to search cross linked peptide data derived from Protein Interaction Reporter (PIR) methods using the spectral library search algorithm, SpectraST. Spectral library matching of cross-linked peptide data from query spectra increased the absolute number of confident peptide relationships matched to spectra and thereby the number of PPIs identified. By matching library spectra from bona fide, previously established PIR-cross-linked peptide relationships, spectral library searching reduces the need for continued, complex mass spectrometric methods to identify peptide relationships, increases coverage of relationship identifications, and improves the accessibility of XL-MS technologies.
引用
收藏
页码:1725 / 1731
页数:7
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