The repeat domain of the melanosome fibril protein Pmel17 forms the amyloid core promoting melanin synthesis

Proc Natl Acad Sci U S A. 2009 Aug 18;106(33):13731-6. doi: 10.1073/pnas.0906509106. Epub 2009 Jul 31.

Abstract

Pmel17 is a melanocyte protein necessary for eumelanin deposition 1 in mammals and found in melanosomes in a filamentous form. The luminal part of human Pmel17 includes a region (RPT) with 10 copies of a partial repeat sequence, pt.e.gttp.qv., known to be essential in vivo for filament formation. We show that this RPT region readily forms amyloid in vitro, but only under the mildly acidic conditions typical of the lysosome-like melanosome lumen, and the filaments quickly become soluble at neutral pH. Under the same mildly acidic conditions, the Pmel filaments promote eumelanin formation. Electron diffraction, circular dichroism, and solid-state NMR studies of Pmel17 filaments show that the structure is rich in beta sheet. We suggest that RPT is the amyloid core domain of the Pmel17 filaments so critical for melanin formation.

Publication types

  • Research Support, N.I.H., Intramural

MeSH terms

  • Amino Acid Sequence
  • Amyloid / chemistry*
  • Humans
  • Hydrogen-Ion Concentration
  • Magnetic Resonance Spectroscopy
  • Melanins / chemistry*
  • Melanocytes / metabolism
  • Melanosomes / metabolism*
  • Membrane Glycoproteins / chemistry*
  • Microscopy, Electron, Transmission
  • Models, Biological
  • Molecular Sequence Data
  • Protein Structure, Tertiary
  • Sequence Homology, Amino Acid
  • gp100 Melanoma Antigen

Substances

  • Amyloid
  • Melanins
  • Membrane Glycoproteins
  • PMEL protein, human
  • gp100 Melanoma Antigen
  • eumelanin