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Gopalswamy, M. ; Zheng, C.* ; Gaussmann, S. ; Kooshapur, H. ; Hambruch, E.* ; Schliebs, W.* ; Erdmann, R.* ; Antes, I.* ; Sattler, M.

Distinct conformational and energetic features define the specific recognition of (di)aromatic peptide motifs by PEX14.

Biol. Chem., DOI: 10.1515/hsz-2022-0177 (2022)
Postprint DOI PMC
Open Access Gold (Paid Option)
The cycling import receptor PEX5 and its membrane-located binding partner PEX14 are key constituents of the peroxisomal import machinery. Upon recognition of newly synthesized cargo proteins carrying a peroxisomal targeting signal type 1 (PTS1) in the cytosol, the PEX5/cargo complex docks at the peroxisomal membrane by binding to PEX14. The PEX14 N-terminal domain (NTD) recognizes (di)aromatic peptides, mostly corresponding to Wxxx(F/Y)-motifs, with nano-to micromolar affinity. Human PEX5 possesses eight of these conserved motifs distributed within its 320-residue disordered N-terminal region. Here, we combine biophysical (ITC, NMR, CD), biochemical and computational methods to characterize the recognition of these (di)aromatic peptides motifs and identify key features that are recognized by PEX14. Notably, the eight motifs present in human PEX5 exhibit distinct affinities and energetic contributions for the interaction with the PEX14 NTD. Computational docking and analysis of the interactions of the (di)aromatic motifs identify the specific amino acids features that stabilize a helical conformation of the peptide ligands and mediate interactions with PEX14 NTD. We propose a refined consensus motif ExWΦxE(F/Y)Φ for high affinity binding to the PEX14 NTD and discuss conservation of the (di)aromatic peptide recognition by PEX14 in other species.
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Publication type Article: Journal article
Document type Scientific Article
Corresponding Author
Keywords Nmr ; Wxxx(f/y) Motifs ; Isothermal Titration Calorimetry ; Molecular Dynamics ; Peroxisome Biogenesis ; Protein-protein Interactions
ISSN (print) / ISBN 1431-6730
e-ISSN 1437-4315
Journal Biological Chemistry
Publisher de Gruyter
Non-patent literature Publications
Reviewing status Peer reviewed
Institute(s) Institute of Structural Biology (STB)
Grants Deutsche Forschungsgemeinschaft