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Tim50(164 - 361)的结构揭示了Tim50接收线粒体前序列的机制。

The structure of Tim50(164-361) suggests the mechanism by which Tim50 receives mitochondrial presequences.

作者信息

Li Jingzhi, Sha Bingdong

机构信息

Department of Cell, Developmental and Integrative Biology (CDIB), University of Alabama at Birmingham, Birmingham, AL 35294, USA.

出版信息

Acta Crystallogr F Struct Biol Commun. 2015 Sep;71(Pt 9):1146-51. doi: 10.1107/S2053230X15013102. Epub 2015 Aug 25.

Abstract

Mitochondrial preproteins are transported through the translocase of the outer membrane (TOM) complex. Tim50 and Tim23 then transfer preproteins with N-terminal targeting presequences through the intermembrane space (IMS) across the inner membrane. The crystal structure of the IMS domain of Tim50 [Tim50(164-361)] has previously been determined to 1.83 Å resolution. Here, the crystal structure of Tim50(164-361) at 2.67 Å resolution that was crystallized using a different condition is reported. Compared with the previously determined Tim50(164-361) structure, significant conformational changes occur within the protruding β-hairpin of Tim50 and the nearby helix A2. These findings indicate that the IMS domain of Tim50 exhibits significant structural plasticity within the putative presequence-binding groove, which may play important roles in the function of Tim50 as a receptor protein in the TIM complex that interacts with the presequence and multiple other proteins. More interestingly, the crystal packing indicates that helix A1 from the neighboring monomer docks into the putative presequence-binding groove of Tim50(164-361), which may mimic the scenario of Tim50 and the presequence complex. Tim50 may recognize and bind the presequence helix by utilizing the inner side of the protruding β-hairpin through hydrophobic interactions. Therefore, the protruding β-hairpin of Tim50 may play critical roles in receiving the presequence and recruiting Tim23 for subsequent protein translocations.

摘要

线粒体前体蛋白通过外膜转位酶(TOM)复合体进行转运。然后,Tim50和Tim23将带有N端靶向前导序列的前体蛋白通过膜间隙(IMS)转运穿过内膜。Tim50的IMS结构域[Tim50(164 - 361)]的晶体结构先前已确定为1.83 Å分辨率。在此,报道了在不同条件下结晶得到的分辨率为2.67 Å的Tim50(164 - 361)晶体结构。与先前确定的Tim50(164 - 361)结构相比,Tim50突出的β - 发夹结构及附近的A2螺旋内发生了显著的构象变化。这些发现表明,Tim50的IMS结构域在假定的前导序列结合凹槽内表现出显著的结构可塑性,这可能在Tim50作为TIM复合体中与前导序列及多种其他蛋白质相互作用的受体蛋白的功能中发挥重要作用。更有趣的是,晶体堆积表明来自相邻单体的A1螺旋对接至Tim50(164 - 361)假定的前导序列结合凹槽中,这可能模拟了Tim50与前导序列复合体的情况。Tim50可能通过利用突出的β - 发夹结构的内侧通过疏水相互作用识别并结合前导序列螺旋。因此,Tim50突出的β - 发夹结构可能在接收前导序列和招募Tim23进行后续蛋白质转运中起关键作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e47d/4555921/771c351c6eaf/f-71-01146-fig1.jpg

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