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Sequence-Specific 2-Cyanobenzothiazole Ligation.
Ramil, Carlo P; An, Peng; Yu, Zhipeng; Lin, Qing.
Afiliación
  • Ramil CP; Department of Chemistry, State University of New York at Buffalo , Buffalo, New York 14260, United States.
  • An P; Department of Chemistry, State University of New York at Buffalo , Buffalo, New York 14260, United States.
  • Yu Z; Department of Chemistry, State University of New York at Buffalo , Buffalo, New York 14260, United States.
  • Lin Q; Department of Chemistry, State University of New York at Buffalo , Buffalo, New York 14260, United States.
J Am Chem Soc ; 138(17): 5499-502, 2016 05 04.
Article en En | MEDLINE | ID: mdl-27082895
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 cysteine-encoded 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.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Péptidos / Benzotiazoles / Nitrilos Idioma: En Revista: J Am Chem Soc Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Péptidos / Benzotiazoles / Nitrilos Idioma: En Revista: J Am Chem Soc Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos