Insertion of Pex5p into the peroxisomal membrane is cargo protein-dependent

被引:74
作者
Gouveia, AM
Guimaraes, CP
Oliveira, ME
Sá-Miranda, C
Azevedo, JE
机构
[1] Inst Biol Mol & Celular, P-4150180 Oporto, Portugal
[2] Inst Ciencias Biomed Abel Salazar, P-4099003 Oporto, Portugal
[3] Inst Genet Med Jacinto Magalhaes, P-4050466 Oporto, Portugal
关键词
D O I
10.1074/jbc.C200650200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:4389 / 4392
页数:4
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