Structural and Mechanistic Aspects of Amt/Rh Proteins

J Struct Biol. 2007 Jun;158(3):472-81. doi: 10.1016/j.jsb.2007.01.004. Epub 2007 Jan 23.

Abstract

Amt/Rh proteins, which mediate movement of ammonium across cell membranes, are spread throughout the three kingdoms of life. Most functional studies on various members of the family have been performed using cellular assays in heterologous expression systems, which are, however, not very well suited for detailed mechanistic studies. Although now generally considered to be ammonia conducting channels, based on a number of experimental studies and structural insights, the possibility remains that some plant Amts facilitate net ammonium ion transport. The Escherichia coli channel AmtB has become the model system of choice for analysis of the mechanism of ammonia conductance, increasingly also through molecular dynamics simulations. Further progress in a more detailed mechanistic understanding of these proteins requires a reliable in vitro assay using purified protein, allowing quantitative kinetic measurements under a variety of experimental conditions for different Amt/Rh proteins, including mutants. Here, we critically review the existing functional data in the context of the most interesting and unresolved mechanistic questions and we present our results, obtained using an in vitro assay set up with the purified E. coli channel AmtB.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Biological Assay
  • Cation Transport Proteins / chemistry*
  • Cation Transport Proteins / ultrastructure
  • Escherichia coli Proteins / chemistry*
  • Escherichia coli Proteins / ultrastructure
  • Membrane Glycoproteins / chemistry
  • Membrane Glycoproteins / ultrastructure
  • Models, Biological
  • Protein Conformation
  • Quaternary Ammonium Compounds / metabolism*

Substances

  • AmtB protein, E coli
  • Cation Transport Proteins
  • Escherichia coli Proteins
  • Membrane Glycoproteins
  • Quaternary Ammonium Compounds