Engineering bromodomains with a photoactive amino acid by engaging 'Privileged' tRNA synthetases

  • Shana Wagner
  • , Babu Sudhamalla
  • , Philip Mannes
  • , Sushma Sappa
  • , Sam Kavoosi
  • , Debasis Dey
  • , Sinan Wang
  • , Kabirul Islam

Research output: Contribution to journalArticlepeer-review

Abstract

Site-specific placement of unnatural amino acids, particularly those responsive to light, offers an elegant approach to control protein function and capture their fleeting 'interactome'. Herein, we have resurrected 4-(trifluoromethyldiazirinyl)-phenylalanine, an underutilized photo-crosslinker, by introducing several key features including easy synthetic access, site-specific incorporation by 'privileged' synthetases and superior crosslinking efficiency, to develop photo-crosslinkable bromodomains suitable for 'interactome' profiling.

Original languageEnglish (US)
Pages (from-to)3641-3644
Number of pages4
JournalChemical Communications
Volume56
Issue number25
DOIs
StatePublished - Mar 28 2020

All Science Journal Classification (ASJC) codes

  • Catalysis
  • Electronic, Optical and Magnetic Materials
  • Ceramics and Composites
  • General Chemistry
  • Surfaces, Coatings and Films
  • Metals and Alloys
  • Materials Chemistry

Fingerprint

Dive into the research topics of 'Engineering bromodomains with a photoactive amino acid by engaging 'Privileged' tRNA synthetases'. Together they form a unique fingerprint.

Cite this