Peptide mini-scaffold facilitates JNK3 activation in cells

Sci Rep. 2016 Feb 12:6:21025. doi: 10.1038/srep21025.

Abstract

Three-kinase mitogen-activated protein kinase (MAPK) signaling cascades are present in virtually all eukaryotic cells. MAPK cascades are organized by scaffold proteins, which assemble cognate kinases into productive signaling complexes. Arrestin-3 facilitates JNK activation in cells, and a short 25-residue arrestin-3 peptide was identified as the critical JNK3-binding element. Here we demonstrate that this peptide also binds MKK4, MKK7, and ASK1, which are upstream JNK3-activating kinases. This peptide is sufficient to enhance JNK3 activity in cells. A homologous arrestin-2 peptide, which differs only in four positions, binds MKK4, but not MKK7 or JNK3, and is ineffective in cells at enhancing activation of JNK3. The arrestin-3 peptide is the smallest MAPK scaffold known. This peptide or its mimics can regulate MAPKs, affecting cellular decisions to live or die.

Publication types

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

MeSH terms

  • Animals
  • COS Cells
  • Chlorocebus aethiops
  • Enzyme Activation / drug effects
  • Enzyme Activators* / chemical synthesis
  • Enzyme Activators* / chemistry
  • Enzyme Activators* / pharmacology
  • Humans
  • Mitogen-Activated Protein Kinase 10 / genetics
  • Mitogen-Activated Protein Kinase 10 / metabolism*
  • Peptides* / chemical synthesis
  • Peptides* / chemistry
  • Peptides* / pharmacology
  • beta-Arrestin 1 / chemistry*
  • beta-Arrestin 2 / chemistry*

Substances

  • Enzyme Activators
  • Peptides
  • beta-Arrestin 1
  • beta-Arrestin 2
  • Mitogen-Activated Protein Kinase 10