Skip to Content
Merck
  • Synthesis of a novel histidine analogue and its efficient incorporation into a protein in vivo.

Synthesis of a novel histidine analogue and its efficient incorporation into a protein in vivo.

Protein engineering (2003-10-16)
Yutaka Ikeda, Shun-ichi Kawahara, Masumi Taki, Atsushi Kuno, Tsunemi Hasegawa, Kazunari Taira
ABSTRACT

Proteins containing unnatural amino acids have immense potential in biotechnology and medicine. We prepared several histidine analogues including a novel histidine analogue, beta-(1,2,3-triazol-4-yl)-DL-alanine. These histidine analogues were assayed for translational activity in histidine-auxotrophic Escherichia coli strain UTH780. We observed that several histidine analogues, including our novel histidine analogue, were efficiently incorporated into the protein in vivo; however, other analogues were rejected. These results suggest that the hydrogen atom at a specific position seriously affects incorporation.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
β-(1,2,4-Triazol-3-yl)-DL-alanine