Gouveia Alexandra M, Guimarães Carla P, Oliveira Márcia E, Sá-Miranda Clara, Azevedo Jorge E
Instituto de Biologia Molecular e Celular, Rua do Campo Alegre, 823, 4150-180 Porto, Portugal.
J Biol Chem. 2003 Feb 14;278(7):4389-92. doi: 10.1074/jbc.C200650200. Epub 2002 Dec 26.
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.
现在人们普遍认为,大多数过氧化物酶体基质蛋白的受体Pex5p在细胞质和过氧化物酶体区室之间循环。根据目前过氧化物酶体生物发生的模型,Pex5p的这种细胞内运输与新合成的过氧化物酶体蛋白向细胞器基质的运输相关联。然而,从未提供支持这一假设的直接证据。在这里,我们使用体外过氧化物酶体导入系统表明,Pex5p插入过氧化物酶体膜需要货物蛋白的存在。引人注目的是,过氧化物酶体对接/易位机制也能够催化缺乏任何已知货物结合结构域的Pex5p截短分子的膜插入。这些结果表明,Pex5p参与的细胞质/过氧化物酶体循环是直接或间接受Pex5p自身调节,而不是受 过氧化物酶体对接/易位机制调节。