Skip to main navigation Skip to search Skip to main content

Sequence-specific 2-cyanobenzothiazole ligation

  • Carlo P. Ramil
  • , Peng An
  • , Zhipeng Yu
  • , Qing Lin
  • SUNY Buffalo
  • Sichuan University

Research output: Contribution to journalArticlepeer-review

56 Scopus citations

Abstract

The use of small, natural chemical reporters in conjunction with catalyst-free bioorthogonal reactions will greatly streamline protein labeling in a cellular environment with minimum perturbation to their function. Here we report the discovery of a 2-cyanobenzothiazole (CBT)-reactive peptide tag, CX10R7, from a cysteineencoded peptide phage library using the phage-assisted interrogation of reactivity method. Fusion of CX10R7 with a protein of interest allows site-specific labeling of the protein with CBT both in vitro and on the surface of E. coli cells. Mutagenesis studies indicated that the reactivity and specificity of CX10R7 are attributed to the sequence environment, in which the residues surrounding cysteine help to stabilize the ligation product.

Original languageEnglish
Pages (from-to)5499-5502
Number of pages4
JournalJournal of the American Chemical Society
Volume138
Issue number17
DOIs
StatePublished - May 4 2016

Fingerprint

Dive into the research topics of 'Sequence-specific 2-cyanobenzothiazole ligation'. Together they form a unique fingerprint.

Cite this