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Active and passive displacement of transmembrane domains both occur during opsin biogenesis at the Sec61 translocon

机译:跨膜结构域的主动和被动置换均发生在视蛋白生物发生期间的Sec61转运子上。

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We used a site-specific crosslinking approach to study the membrane integration of the polytopic protein opsin at the endoplasmic reticulum. We show that transmembrane domain 1 occupies two distinct Sec61-based environments during its integration. However, transmembrane domains 2 and 3 exit the Sec61 translocon more rapidly in a process that suggests a displacement model for their integration where the biosynthesis of one transmembrane domain would facilitate the exit of another. In order to investigate this hypothesis further, we studied the integration of the first and third transmembrane domains of opsin in the absence of any additional C-terminal transmembrane domains. In the case of transmembrane domain 1, we found that its lateral exit from the translocon is clearly dependent upon the synthesis of subsequent transmembrane domains. By contrast, the lateral exit of the third transmembrane domain occurred independently of any such requirement. Thus, even within a single polypeptide chain, distinct transmembrane domains display different requirements for their integration through the endoplasmic reticulum translocon, and the displacement of one transmembrane domain by another is not a global requirement for membrane integration.
机译:我们使用了一种特定于站点的交联方法来研究内质网上的多聚蛋白视蛋白的膜整合。我们显示跨膜域1在其集成过程中占据两个不同的基于Sec61的环境。但是,跨膜结构域2和3在建议整合它们的位移模型的过程中更快速地退出Sec61 translocon,其中一个跨膜结构域的生物合成将促进另一个结构域的退出。为了进一步研究该假设,我们研究了在没有任何其他C端跨膜结构域的情况下视蛋白的第一个和第三个跨膜结构域的整合。在跨膜结构域1的情况下,我们发现其从translocon的侧向出口显然取决于后续跨膜结构域的合成。相比之下,第三跨膜结构域的侧向出口独立于任何此类要求而发生。因此,即使在单个多肽链中,不同的跨膜结构域对于通过内质网translocon整合也显示出不同的要求,并且一个跨膜结构域被另一个跨膜结构域取代并不是膜整合的全局要求。

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