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A Click-Chemistry-Based Enrichable Crosslinker for Structural and Protein Interaction Analysis by Mass Spectrometry.

Author(s): Stadlmeier, Michael; Runtsch, Leander Simon; Streshnev, Filipp; Wühr, Martin; Carell, Thomas

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Abstract: Mass spectrometry is the method of choice for the characterisation of proteomes. Most proteins operate in protein complexes, in which their close association modulates their function. However, with standard MS analysis, information on protein-protein interactions is lost and no structural information is retained. To gain structural and interactome data, new crosslinking reagents are needed that freeze inter- and intramolecular interactions. Herein, the development of a new reagent, which has several features that enable highly sensitive crosslinking MS, is reported. The reagent enables enrichment of crosslinked peptides from the majority of background peptides to facilitate efficient detection of low-abundant crosslinked peptides. Due to the special cleavable properties, the reagent can be used for MS2 and potentially for MS3 experiments. Thus, the new crosslinking reagent, in combination with high-end MS, should enable sensitive analysis of interactomes, which will help researchers to obtain important insights into cellular states in health and diseases.
Publication Date: Jan-2020
Citation: Stadlmeier, Michael, Runtsch, Leander Simon, Streshnev, Filipp, Wühr, Martin, Carell, Thomas. (2020). A Click-Chemistry-Based Enrichable Crosslinker for Structural and Protein Interaction Analysis by Mass Spectrometry. Chembiochem : a European journal of chemical biology, 21 (1-2), 103 - 107. doi:10.1002/cbic.201900611
DOI: doi:10.1002/cbic.201900611
ISSN: 1439-4227
EISSN: 1439-7633
Pages: 103 - 107
Language: eng
Type of Material: Journal Article
Journal/Proceeding Title: Chembiochem : a European journal of chemical biology
Version: Final published version. This is an open access article.



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