Structure-Based Engineering of Lithium-Transport Capacity in an Archaeal Sodium-Calcium Exchanger

Biochemistry. 2016 Mar 29;55(12):1673-6. doi: 10.1021/acs.biochem.6b00119. Epub 2016 Mar 10.

Abstract

Members of the Ca(2+)/cation exchanger superfamily (Ca(2+)/CA) share structural similarities (including highly conserved ion-coordinating residues) while exhibiting differential selectivity for Ca(2+), Na(+), H(+), K(+), and Li(+). The archaeal Na(+)/Ca(2+) exchanger (NCX_Mj) and its mammalian orthologs are highly selective for Na(+), whereas the mitochondrial ortholog (NCLX) can transport either Li(+) or Na(+) in exchange with Ca(2+). Here, structure-based replacement of ion-coordinating residues in NCX_Mj resulted in a capacity for transporting either Na(+) or Li(+), similar to the case for NCLX. This engineered protein may serve as a model for elucidating the mechanisms underlying ion selectivity and ion-coupled alternating access in NCX and similar proteins.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Escherichia coli Proteins / chemistry*
  • Escherichia coli Proteins / genetics
  • Escherichia coli Proteins / metabolism
  • Ion Transport / physiology
  • Lithium / metabolism*
  • Molecular Sequence Data
  • Protein Engineering / methods*
  • Sodium-Calcium Exchanger / chemistry*
  • Sodium-Calcium Exchanger / genetics
  • Sodium-Calcium Exchanger / metabolism*
  • Structure-Activity Relationship

Substances

  • Escherichia coli Proteins
  • Sodium-Calcium Exchanger
  • Lithium