The difference in recognition of terminal tripeptides as peroxisomal targeting signal 1 between yeast and human is due to different affinities of their receptor Pex5p to the cognate signal and to residues adjacent to it

J Biol Chem. 1998 Dec 11;273(50):33635-43. doi: 10.1074/jbc.273.50.33635.

Abstract

Pex5p is the receptor for the peroxisomal targeting signal 1 (PTS1) that consists of a C-terminal tripeptide (consensus (S/A/C)(K/R/H)(L/M)). Hexadecapeptides recognized by Pex5p from Homo sapiens and Saccharomyces cerevisiae were identified by screening a two-hybrid peptide library, and the targeting ability of the peptides was demonstrated using the green fluorescent protein as reporter. The PTS1 receptors recognized in a species-specific manner a broad range of C-terminal tripeptides, and these are reported herein. In addition, residues upstream of the tripeptide influenced the strength of the interaction in the two-hybrid system as well as in an in vitro competition assay. In peptides interacting with the human protein, hydrophobic residues were found with high frequency especially at positions -2 and -5, whereas peptides interacting with S. cerevisiae Pex5p were more hydrophilic and frequently contained arginine at position -2. In instances where the terminal tripeptide deviated from the consensus, upstream residues exerted a greater influence on the ability of the hexadecapeptides to bind Pex5p.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Base Sequence
  • DNA Primers
  • Humans
  • Microbodies / metabolism*
  • Molecular Sequence Data
  • Oligopeptides / metabolism*
  • Peroxisome-Targeting Signal 1 Receptor
  • Protein Binding
  • Protein Sorting Signals / metabolism*
  • Receptors, Cytoplasmic and Nuclear / chemistry
  • Receptors, Cytoplasmic and Nuclear / metabolism*
  • Saccharomyces cerevisiae / metabolism*
  • Sequence Homology, Amino Acid

Substances

  • DNA Primers
  • Oligopeptides
  • Peroxisome-Targeting Signal 1 Receptor
  • Protein Sorting Signals
  • Receptors, Cytoplasmic and Nuclear