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激活军团菌 LegK7 效应激酶的宿主 MOB1 蛋白。

Activation of the Legionella pneumophila LegK7 Effector Kinase by the Host MOB1 Protein.

机构信息

Division of Biomedical Convergence, College of Biomedical Science, Kangwon National University, Chuncheon 24341, Republic of Korea.

Institute of Bioscience and Biotechnology, Kangwon National University, Chuncheon 24341, Republic of Korea.

出版信息

J Mol Biol. 2021 Feb 5;433(3):166746. doi: 10.1016/j.jmb.2020.166746. Epub 2020 Dec 10.

Abstract

Legionella pneumophila infects alveolar macrophages and can cause life-threatening pneumonia in humans. Upon internalization into the host cell, L. pneumophila injects numerous effector proteins into the host cytoplasm as a part of its pathogenesis. LegK7 is an effector kinase of L. pneumophila that functionally mimics the eukaryotic Mst kinase and phosphorylates the host MOB1 protein to exploit the Hippo pathway. To elucidate the LegK7 activation mechanism, we determined the apo structure of LegK7 in an inactive form and performed a comparative analysis of LegK7 structures. LegK7 is a non-RD kinase that contains an activation segment that is ordered, irrespective of stimulation, through a unique β-hairpin-containing segment, and it does not require phosphorylation of the activation segment for activation. Instead, bacterial LegK7 becomes an active kinase via its heterologous molecular interaction with the host MOB1 protein. MOB1 binding triggers reorientation of the two lobes of the kinase domain, as well as a structural change in the interlobe hinge region in LegK7, consequently reshaping the LegK7 structure into an ATP binding-compatible closed conformation. Furthermore, we reveal that LegK7 is an atypical kinase that contains an N-terminal capping domain and a hydrophilic interlobe linker motif, which play key roles in the MOB1-induced activation of LegK7.

摘要

嗜肺军团菌感染肺泡巨噬细胞,并可导致人类的致命性肺炎。在被宿主细胞内化后,嗜肺军团菌将大量效应蛋白注入宿主细胞质,作为其发病机制的一部分。LegK7 是嗜肺军团菌的效应激酶,在功能上模拟真核 Mst 激酶,并磷酸化宿主 MOB1 蛋白以利用 Hippo 途径。为了阐明 LegK7 的激活机制,我们测定了 LegK7 在非活性形式下的无配体结构,并对 LegK7 结构进行了比较分析。LegK7 是非 RD 激酶,其包含一个激活片段,该片段通过独特的含有 β-发夹的片段保持有序,而无需激活片段的磷酸化即可激活。相反,细菌 LegK7 通过与宿主 MOB1 蛋白的异源分子相互作用成为活性激酶。MOB1 结合触发激酶结构域两个叶的重新定向,以及 LegK7 中叶间铰链区域的结构变化,从而将 LegK7 结构重塑为与 ATP 结合相容的闭合构象。此外,我们揭示 LegK7 是一种非典型激酶,它包含一个 N 端盖帽结构域和一个亲水的叶间连接基序,这在 MOB1 诱导的 LegK7 激活中起着关键作用。

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