Algorithms for identifying protein cross-links via tandem mass spectrometry

被引:28
作者
Chen, T [1 ]
Jaffe, JD
Church, GM
机构
[1] Univ So Calif, Dept Mol Biol, Los Angeles, CA 90089 USA
[2] Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA
[3] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA
关键词
proteomics; mass spectrometry; algorithms; protein cross-linking; protein-protein interactions; protein folding;
D O I
10.1089/106652701753307494
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Cross-linking technology combined with tandem mass spectrometry (MS-MS) is a powerful method that provides a rapid solution to the discovery of protein-protein interactions and protein structures. We studied the problem of detecting cross-linked peptides and crosslinked amino acids from tandem mass spectral data. Our method consists of two steps: the first step finds two protein subsequences whose mass sum equals a given mass measured from the mass spectrometry; and the second step finds the best cross-linked amino acids in these two peptide sequences that are optimally correlated to a given tandem mass spectrum. We designed fast and space-efficient algorithms for these two steps and implemented and tested them on experimental data of cross-linked hemoglobin proteins. An interchain crosslink between two beta subunits was found in two tandem mass spectra. The length of the cross-linker (7.7 Angstrom) is very close to the actual distance (8.18 Angstrom) obtained from the molecular structure in PDB.
引用
收藏
页码:571 / 583
页数:13
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