Kinetics of iron release from transferrin bound to the transferrin receptor at endosomal pH

Biochim Biophys Acta. 2012 Mar;1820(3):326-33. doi: 10.1016/j.bbagen.2011.06.003. Epub 2011 Jun 15.

Abstract

Background: Human serum transferrin (hTF) is a bilobal glycoprotein that reversibly binds Fe(3+) and delivers it to cells by the process of receptor-mediated endocytosis. Despite decades of research, the precise events resulting in iron release from each lobe of hTF within the endosome have not been fully delineated.

Scope of review: We provide an overview of the kinetics of iron release from hTF±the transferrin receptor (TFR) at endosomal pH (5.6). A critical evaluation of the array of biophysical techniques used to determine accurate rate constants is provided.

General significance: Delivery of Fe(3+)to actively dividing cells by hTF is essential; too much or too little Fe(3+) directly impacts the well-being of an individual. Because the interaction of hTF with the TFR controls iron distribution in the body, an understanding of this process at the molecular level is essential.

Major conclusions: Not only does TFR direct the delivery of iron to the cell through the binding of hTF, kinetic data demonstrate that it also modulates iron release from the N- and C-lobes of hTF. Specifically, the TFR balances the rate of iron release from each lobe, resulting in efficient Fe(3+) release within a physiologically relevant time frame. This article is part of a Special Issue entitled Molecular Mechanisms of Iron Transport and Disorders.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Biological Transport
  • Endocytosis
  • Endosomes / metabolism
  • Humans
  • Hydrogen-Ion Concentration
  • Iron / metabolism*
  • Protein Conformation
  • Receptors, Transferrin / chemistry
  • Receptors, Transferrin / metabolism*
  • Transferrin / metabolism*

Substances

  • Receptors, Transferrin
  • Transferrin
  • Iron