Molecular Basis of Metal-Ion Selectivity and Zeptomolar Sensitivity by CueR
Northwestern University · Northwest University
Abstract
The earliest of a series of copper efflux genes in Escherichia coli are controlled by CueR, a member of the MerR family of transcriptional activators. Thermodynamic calibration of CueR reveals a zeptomolar (10(-21) molar) sensitivity to free Cu+, which is far less than one atom per cell. Atomic details of this extraordinary sensitivity and selectivity for +1transition-metal ions are revealed by comparing the crystal structures of CueR and a Zn2+-sensing homolog, ZntR. An unusual buried metal-receptor site in CueR restricts the metal to a linear, two-coordinate geometry and uses helix-dipole and hydrogen-bonding interactions to enhance metal binding. This binding mode is rare among metalloproteins but well…
Citation impact
- FWCI
- 17.81
- Percentile
- 100%
- References
- 33
Authors
7- ACAnita ChangelaCorresponding
Northwestern University, Northwest University
- KCKui ChenCorresponding
Northwestern University, Northwest University
- YXYi Xue
Northwestern University, Northwest University
- JHJ. Holschen
Northwestern University, Northwest University
- CECaryn E. Outten
Northwestern University, Northwest University
Topics & keywords
- Chemistry
- Metalloprotein
- Metal ions in aqueous solution
- Metal
- Binding site
- Crystallography
- Ion
- Selectivity