Graduate School of Chemical Sciences and Engineering, Hokkaido University, Sapporo, Hokkaido 060-8628, Japan.
Graduate School of Medical Sciences, Tokushima University, Tokushima 770-8503, Japan.
Biochemistry. 2022 Dec 20;61(24):2897-2908. doi: 10.1021/acs.biochem.2c00492. Epub 2022 Dec 9.
A transcriptional regulatory system called heat shock response (HSR) has been developed in eukaryotic cells to maintain proteome homeostasis under various stresses. Heat shock factor-1 (Hsf1) plays a central role in HSR, mainly by upregulating molecular chaperones as a transcription factor. Hsf1 forms a complex with chaperones and exists as a monomer in the resting state under normal conditions. However, upon heat shock, Hsf1 is activated by oligomerization. Thus, oligomerization of Hsf1 is considered an important step in HSR. However, the lack of information about Hsf1 monomer structure in the resting state, as well as the structural change via oligomerization at heat response, impeded the understanding of the thermosensing mechanism through oligomerization. In this study, we applied solution biophysical methods, including fluorescence spectroscopy, nuclear magnetic resonance, and circular dichroism spectroscopy, to investigate the heat-induced conformational transition mechanism of Hsf1 leading to oligomerization. Our study showed that Hsf1 forms an inactive closed conformation mediated by intramolecular contact between leucine zippers (LZs), in which the intermolecular contact between the LZs for oligomerization is prevented. As the temperature increases, Hsf1 changes to an open conformation, where the intramolecular LZ interaction is dissolved so that the LZs can form intermolecular contacts to form oligomers in the active form. Furthermore, since the interaction sites with molecular chaperones and nuclear transporters are also expected to be exposed in the open conformation, the conformational change to the open state can lead to understanding the regulation of Hsf1-mediated stress response through interaction with multiple cellular components.
真核细胞中存在一种称为热休克反应(HSR)的转录调控系统,用于在各种应激条件下维持蛋白质组的平衡。热休克因子-1(Hsf1)在 HSR 中起着核心作用,主要作为转录因子上调分子伴侣。Hsf1 与伴侣形成复合物,并在正常条件下以单体形式存在于静止状态。然而,在受到热冲击时,Hsf1 通过寡聚化而被激活。因此,Hsf1 的寡聚化被认为是 HSR 的重要步骤。然而,由于缺乏静止状态下 Hsf1 单体结构的信息,以及热响应时通过寡聚化的结构变化,阻碍了通过寡聚化理解热感应机制。在这项研究中,我们应用了溶液生物物理方法,包括荧光光谱、核磁共振和圆二色光谱,来研究导致寡聚化的 Hsf1 热诱导构象转变机制。我们的研究表明,Hsf1 通过分子内拉链(LZ)之间的相互作用形成无活性的封闭构象,从而阻止了 LZ 之间用于寡聚化的分子间接触。随着温度的升高,Hsf1 转变为开放构象,其中 LZ 之间的分子内相互作用被溶解,从而使 LZ 能够形成具有活性的寡聚体的分子间接触。此外,由于与分子伴侣和核转运蛋白的相互作用位点也预计在开放构象中暴露,因此向开放状态的构象变化可以通过与多个细胞成分的相互作用来理解 Hsf1 介导的应激反应的调节。