Abstract

It is now generally accepted that Pex5p, the receptor for most peroxisomal matrix proteins, cycles between the cytosol and the peroxisomal compartment. According to current models of peroxisomal biogenesis, this intracellular trafficking of Pex5p is coupled to the transport of newly synthesized peroxisomal proteins into the organelle matrix. However, direct evidence supporting this hypothesis was never provided. Here, using an in vitro peroxisomal import system, we show that insertion of Pex5p into the peroxisomal membrane requires the presence of cargo proteins. Strikingly the peroxisomal docking/translocation machinery is also able to catalyze the membrane insertion of a Pex5p truncated molecule lacking any known cargo-binding domain. These results suggest that the cytosol/peroxisomal cycle in which Pex5p is involved is directly or indirectly regulated by Pex5p itself and not by the peroxisomal docking/translocation machinery.

Highlights

  • From the ‡Instituto de Biologia Molecular e Celular, Rua do Campo Alegre, 823, 4150-180 Porto, Portugal, §Instituto de Ciencias Biomedicas Abel Salazar, Largo do Prof

  • The peroxisomal docking/translocation machinery is able to catalyze the membrane insertion of a Pex5p truncated molecule lacking any known cargo-binding domain. These results suggest that the cytosol/peroxisomal cycle in which Pex5p is involved is directly or indirectly regulated by Pex5p itself and not by the peroxisomal docking/translocation machinery

  • A truncated Pex5p molecule lacking any known cargo-binding domain is a substrate for the machinery that drives insertion of Pex5p into the peroxisomal membrane. These results suggest that no crucial protein-protein interactions occur between the peroxisomal docking/translocation machinery (20 –22) on one side and the cargo proteins or the Pex5p C-terminal receptor domain on the other

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Summary

Introduction

From the ‡Instituto de Biologia Molecular e Celular, Rua do Campo Alegre, 823, 4150-180 Porto, Portugal, §Instituto de Ciencias Biomedicas Abel Salazar, Largo do Prof. Using an in vitro peroxisomal import system, we show that insertion of Pex5p into the peroxisomal membrane requires the presence of cargo proteins.

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