Department of Pathology, The University of Michigan Medical School, Ann Arbor, Michigan 48109, USA.
J Biol Chem. 2010 May 21;285(21):15714-23. doi: 10.1074/jbc.M109.098806. Epub 2010 Mar 26.
The Hsp90/Hsp70-based chaperone machinery regulates the activity and degradation of many signaling proteins. Cycling with Hsp90 stabilizes client proteins, whereas Hsp70 interacts with chaperone-dependent E3 ubiquitin ligases to promote protein degradation. To probe these actions, small molecule inhibitors of Hsp70 would be extremely useful; however, few have been identified. Here we test the effects of methylene blue, a recently described inhibitor of Hsp70 ATPase activity, in three well established systems of increasing complexity. First, we demonstrate that methylene blue inhibits the ability of the purified Hsp90/Hsp70-based chaperone machinery to enable ligand binding by the glucocorticoid receptor and show that this effect is due to specific inhibition of Hsp70. Next, we establish that ubiquitination of neuronal nitric-oxide synthase by the native ubiquitinating system of reticulocyte lysate is dependent upon both Hsp70 and the E3 ubiquitin ligase CHIP and is blocked by methylene blue. Finally, we demonstrate that methylene blue impairs degradation of the polyglutamine expanded androgen receptor, an Hsp90 client mutated in spinal and bulbar muscular atrophy. In contrast, degradation of an amino-terminal fragment of the receptor, which lacks the ligand binding domain and, therefore, is not a client of the Hsp90/Hsp70-based chaperone machinery, is enhanced through homeostatic induction of autophagy that occurs when Hsp70-dependent proteasomal degradation is inhibited by methylene blue. Our data demonstrate the utility of methylene blue in defining Hsp70-dependent functions and reveal divergent effects on polyglutamine protein degradation depending on whether the substrate is an Hsp90 client.
Hsp90/Hsp70 基伴侣蛋白机器调节许多信号蛋白的活性和降解。与 Hsp90 循环稳定客户蛋白,而 Hsp70 与伴侣蛋白依赖的 E3 泛素连接酶相互作用,促进蛋白降解。为了探究这些作用,Hsp70 的小分子抑制剂将是非常有用的;然而,很少有被鉴定出来。在这里,我们在三个越来越复杂的成熟系统中测试了亚甲蓝,一种最近描述的 Hsp70 ATP 酶活性抑制剂的效果。首先,我们证明亚甲蓝抑制了纯化的 Hsp90/Hsp70 基伴侣蛋白机器使糖皮质激素受体结合配体的能力,并表明这种效应是由于 Hsp70 的特异性抑制。接下来,我们确定了天然的网织红细胞裂解物的泛素化系统中神经元一氧化氮合酶的泛素化依赖于 Hsp70 和 E3 泛素连接酶 CHIP,并被亚甲蓝阻断。最后,我们证明亚甲蓝损害了多聚谷氨酰胺扩展雄激素受体的降解,该受体是脊髓性肌萎缩症和延髓性肌萎缩症中突变的 Hsp90 客户。相比之下,缺乏配体结合域的受体氨基末端片段的降解,因此不是 Hsp90/Hsp70 基伴侣蛋白机器的客户,通过自噬的同源诱导增强,当 Hsp70 依赖性蛋白酶体降解被亚甲蓝抑制时,会发生自噬。我们的数据证明了亚甲蓝在定义 Hsp70 依赖性功能方面的效用,并揭示了多聚谷氨酰胺蛋白降解的不同影响,这取决于底物是否是 Hsp90 的客户。