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Complementary Benzophenone Cross-Linking/Mass Spectrometry Photochemistry.
Belsom, Adam; Mudd, Gemma; Giese, Sven; Auer, Manfred; Rappsilber, Juri.
Affiliation
  • Belsom A; Wellcome Trust Centre for Cell Biology, Institute of Cell Biology, School of Biological Sciences, University of Edinburgh , Edinburgh EH9 3BF, U.K.
  • Mudd G; School of Biological Sciences and Medical School, University of Edinburgh , Edinburgh EH9 3BF, U.K.
  • Giese S; Chair of Bioanalytics, Institute of Biotechnology, Technische Universität Berlin , 13355 Berlin, Germany.
  • Auer M; School of Biological Sciences and Medical School, University of Edinburgh , Edinburgh EH9 3BF, U.K.
  • Rappsilber J; Wellcome Trust Centre for Cell Biology, Institute of Cell Biology, School of Biological Sciences, University of Edinburgh , Edinburgh EH9 3BF, U.K.
Anal Chem ; 89(10): 5319-5324, 2017 05 16.
Article in En | MEDLINE | ID: mdl-28430416
Use of a heterobifunctional photoactivatable cross-linker, sulfo-SDA (diazirine), has yielded high-density data that facilitated structure modeling of individual proteins. We expand the photoactivatable chemistry toolbox here with a second reagent, sulfo-SBP (benzophenone). This further increases the density of photo-cross-linking to a factor of 20× over conventional cross-linking. Importantly, the two different photoactivatable groups display orthogonal directionality, enabling access to different protein regions, unreachable with a single cross-linker.

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: Anal Chem Year: 2017 Document type: Article Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: Anal Chem Year: 2017 Document type: Article Country of publication: United States