Isotopically labeled crosslinking reagents: Resolution of mass degeneracy in the identification of crosslinked peptides

被引:43
作者
Collins, CJ
Schilling, B
Young, ML
Dollinger, G
Guy, RK [1 ]
机构
[1] Univ Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Cellular & Mol Pharmacol, San Francisco, CA 94143 USA
[3] Sandia Natl Labs, Biosyst Res Dept, Livermore, CA 94551 USA
[4] Chiron Corp, Small Mol Drug Discovery, Emeryville, CA 94608 USA
关键词
D O I
10.1016/j.bmcl.2003.08.053
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Mass spectrometry in three dimensions (MS3D) is a newly developed method for the determination of protein structures involving intramolecular chemical crosslinking of proteins, proteolytic digestion of the resulting adducts, identification of crosslinks by mass spectrometry (MS), peak assignment using theoretical mass lists, and computational reduction of crosslinks to a structure by distance geometry methods. To facilitate the unambiguous identification of crosslinked peptides from proteolytic digestion mixtures of crosslinked proteins by MS, we introduced double O-18 isotopic labels into the crosslinking reagent to provide the crosslinked peptides with a characteristic isotope pattern. The presence of doublets separated by 4 Da in the mass spectra of these materials allowed ready discrimination between crosslinked and modified peptides, and uncrosslinked peptides using automated intelligent data acquisition (IDA) of MS/MS data. This should allow ready automation of the method for application to whole expressible proteomes. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4023 / 4026
页数:4
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