An engineered azurin with a lanthanide binding site capable of copper sensing

Yujia Jiang, Binbin Su, Honghui Chen, Tongtong Zhang, Haiping Liu, Yang Yu*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

1 Citation (Scopus)

Abstract

Proteins with hetero-bimetallic metal centers can catalyze important reactions and are challenging to design. Azurin is a mononuclear copper center that has been extensively studied for electron transfer. Here we inserted the lanthanide binding tag (LBT), which binds lanthanide with sub μM affinity, into the copper binding loop of azurin, while keeping the type 1 copper center unperturbed. The resulting protein, Az-LBT, which has two metal bonding centers, shows strong luminescence upon coordination with Tb3+ and luminescence quenching upon Cu2+ binding. The in vitro luminescence quenching has high metal specificity and a limit-of-detection of 0.65 μM for Cu2+. With the low background from lanthanide's long luminescence lifetime, bacterial cells expressing Az-LBT in the periplasm also shows sensitivity for metal sensing.

Original languageEnglish
Pages (from-to)40-44
Number of pages5
JournalBiochemical and Biophysical Research Communications
Volume561
DOIs
Publication statusPublished - 5 Jul 2021

Keywords

  • Azurin
  • Copper sensing
  • Lanthanide binding tag
  • Luminescence quenching

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