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Novel MS/MS-Cleavable Cross-Linkers: Synthesis, Evaluation of Fragmentation Behavior, and Application for Protein Structure Analysis

Subject Area Analytical Chemistry
Term from 2011 to 2020
Project identifier Deutsche Forschungsgemeinschaft (DFG) - Project number 196601425
 
Final Report Year 2020

Final Report Abstract

Chemical cross-linking in combination with mass spectrometry (XL-MS) has evolved into an alternative strategy for elucidating three-dimensional protein structures and for mapping protein interfaces. In the DFG-funded projects novel collision-induced dissociation (CID)-MS/MS labile cross-linkers were designed, synthesized, and successfully applied to address important biological questions. Our most prominent cross-linker containing a CID-labile urea group (disuccinimidyl dibutyric urea, DSBU, formerly BuUrBu) has become commercially available and is currently in use for conducting XL-MS studies by a number of groups worldwide. The projects have been extraordinarily successful and ultimately resulted in a fully automated analytical workflow that for conducting XL-MS of whole proteomes. This workflow, published in Nature Protocols (2018) and Anal. Chem. (2019), has gained great interest within the community of structural biologists to map protein-protein interaction networks and to determine protein conformations in the complex cellular environment.

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