Histidine-rich proteins (filaggrins): structural and functional heterogeneity during epidermal differentiation

J Mol Biol. 1983 Nov 5;170(3):651-73. doi: 10.1016/s0022-2836(83)80126-0.

Abstract

The urea-soluble protein profiles of guinea pig, rat, mouse and human epidermis have been compared by non-equilibrium pH gradient/sodium dodecyl sulphate two-dimensional gel electrophoresis. The histidine-rich proteins (filaggrins) were identified firstly by their characteristic specificity and kinetics of labelling with [3H]histidine and [32P]phosphate, and secondly by their ability in vitro to aggregate keratin filaments specifically into bundles. In all species the phosphorylated filaggrin precursor, profilaggrin, is resolved as a single or doublet band with an apparent molecular weight greater than 300,000 and a neutral or slightly acidic iso-electric point. In striking contrast, the strongly basic filaggrins produced from similar profilaggrins form molecular weight families that are clearly species specific. In rat and man there is a single, principal molecular weight form of filaggrin (Mr 45,000 and 38,000, respectively), while mouse and guinea pig have heterogeneous families, including high molecular weight variants (Mr greater than 200,000). Even filaggrins of a particular molecular weight are not homogeneous proteins, but consist of a number of iso-electric variants, some of which are considerably less basic than the bulk of the filaggrins. Incorporation studies using [3H]arginine and [32P]phosphate indicate that the iso-electric variance is not due to residual phosphate, following profilaggrin breakdown, but rather to a conversion of basic arginine residues into neutral citrulline residues. Filaggrins of all the molecular weights from all the species studied share the ability to aggregate keratin filaments into large, insoluble macrofibrils. However, the more acidic iso-electric variants have lower affinities for keratin, particularly in man and guinea pig where the most acidic filaggrins have completely lost the ability to aggregate keratins. We discuss the possibility that a loss of keratin binding ability, resulting in a loosening of the keratin fibre/filaggrin matrix is necessary before the normal complete proteolysis of the filaggrins can occur.

MeSH terms

  • Amino Acids / analysis
  • Animals
  • Cell Differentiation
  • Electrophoresis, Polyacrylamide Gel
  • Epidermal Cells
  • Epidermis / metabolism*
  • Filaggrin Proteins
  • Guinea Pigs
  • Histidine / metabolism
  • Humans
  • In Vitro Techniques
  • Intermediate Filament Proteins / metabolism*
  • Keratins / metabolism
  • Mice
  • Protein Precursors / metabolism
  • Rats
  • Species Specificity

Substances

  • Amino Acids
  • FLG protein, human
  • Filaggrin Proteins
  • Intermediate Filament Proteins
  • Protein Precursors
  • Histidine
  • Keratins