xComb: A Cross-Linked Peptide Database Approach to Protein-Protein Interaction Analysis

被引:56
作者
Panchaud, Alexandre [1 ]
Singh, Pragya [1 ]
Shaffer, Scott A. [1 ]
Goodlett, David R. [1 ]
机构
[1] Univ Washington, Dept Med Chem, Seattle, WA 98195 USA
基金
瑞士国家科学基金会; 美国国家卫生研究院;
关键词
Cross-linking; mass spectrometry; protein-protein interaction; CXMS; software; MASS-SPECTROMETRY DATA; SEQUENCE DATABASES; LINKING; IDENTIFICATION; TANDEM; STRATEGY; SPECTRA; REAGENT;
D O I
10.1021/pr9011816
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We developed an informatic method to identify tandem mass spectra composed of chemically crosslinked peptides from those of linear peptides and to assign sequence to each of the two unique peptide sequences. For a given set of proteins the key software tool, xComb, combs through all theoretically feasible cross-linked peptides to create a database consisting of a subset of all combinations represented as peptide FASTA files. The xComb library of select theoretical cross-linked peptides may then be used as a database that is examined by a standard proteomic search engine to match tandem mass spectral data sets to identify cross-linked peptides. The database search may be conducted against as many as 50 proteins with a number of common proteomic search engines, e.g. Phenyx, Sequest, OMSSA, Mascot and XITandem. By searching against a peptide library of linearized, cross-linked peptides, rather than a linearized protein library, search times are decreased and the process is decoupled from any specific search engine. A further benefit of decoupling from the search engine is that protein cross-linking studies may be conducted with readily available informatics tools for which scoring routines already exist within the proteomic community.
引用
收藏
页码:2508 / 2515
页数:8
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