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J Cell Biol. 2019 Jun 3;218(6):2021-2034. doi: 10.1083/jcb.201901152. Epub 2019 Apr 10.

Peroxisome protein import recapitulated in Xenopus egg extracts.

Author information

1
Howard Hughes Medical Institute and Department of Cell Biology, Harvard Medical School, Boston, MA.
2
Howard Hughes Medical Institute and Department of Cell Biology, Harvard Medical School, Boston, MA tom_rapoport@hms.harvard.edu.

Abstract

Peroxisomes import their luminal proteins from the cytosol. Most substrates contain a C-terminal Ser-Lys-Leu (SKL) sequence that is recognized by the receptor Pex5. Pex5 binds to peroxisomes via a docking complex containing Pex14, and recycles back into the cytosol following its mono-ubiquitination at a conserved Cys residue. The mechanism of peroxisome protein import remains incompletely understood. Here, we developed an in vitro import system based on Xenopus egg extracts. Import is dependent on the SKL motif in the substrate and on the presence of Pex5 and Pex14, and is sustained by ATP hydrolysis. A protein lacking an SKL sequence can be coimported, providing strong evidence for import of a folded protein. The conserved cysteine in Pex5 is not essential for import or to clear import sites for subsequent rounds of translocation. This new in vitro assay will be useful for further dissecting the mechanism of peroxisome protein import.

PMID:
30971414
PMCID:
PMC6548129
[Available on 2019-12-28]
DOI:
10.1083/jcb.201901152

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