Xu Z, Pal J K, Thulasiraman V, Hahn H P, Chen J J, Matts R L
Department of Biochemistry and Molecular Biology, Oklahoma State University, Stillwater 74078-3035, USA.
Eur J Biochem. 1997 Jun 1;246(2):461-70. doi: 10.1111/j.1432-1033.1997.t01-1-00461.x.
The heme-regulated eIF-2alpha kinase (HRI) is activated not only in heme-deficient rabbit reticulocyte lysates (RRL), but also in hemin-supplemented RRL treated with heat-shock, N-ethylmaleimide (MalNEt) or heavy metal ions. We have demonstrated previously that heat-shock proteins, Hsp90, Hsp70 and FKBP52, are associated with HRI in RRL; the association of HRI with Hsp90 and FKBP52, but not Hsp70, is enhanced by hemin. To study the role of Hsp90 and its associated cohorts in the regulation of HRI, we examined the interaction of these proteins with HRI in hemin-supplemented RRLs during heat or oxidative stress. The association of HRI with Hsp90, FKBP52 and p23 was maintained in heat-, MalNEt- or Hg2(+)-treated hemin-supplemented RRL. Glycerol gradient centrifugation and gel filtration on Sephacryl S-300 indicated that neither heat shock nor MalNEt-treatment affected the apparent molecular mass of HRI in hemin supplemented RRL. In addition, active HRI was coimmunoprecipitated with 8D3 anti-Hsp90 from both heme-deficient and MalNEt-treated hemin-supplemented RRL. These results demonstrate that activation of HRI in response to heat stress and oxidative stress does not require dissociation of Hsp90 from HRI. Furthermore, HRI activity was inhibited upon addition of hemin to Hsp90-depleted heme-deficient RRL, indicating that inhibition of HRI activity by hemin is not mediated by the reassociation of Hsp90 with HRI. We also examined the dynamics of the interaction of Hsp90 with HRI. Reconstitution of the interaction of Hsp90 with HRI was stimulated by elevated temperature and required both Mg2+ and ATP. Addition of purified Hsp90 to hemin-supplemented RRL which had been treated with MalNEt to inactivate its capacity to chaperone protein renaturation, protected HRI from irreversible denaturation and aggregation upon incubation at 41 degrees C. Our results suggest that Hsp90 interacts with HRI primarily in its capacity as a molecular chaperone, stabilizing HRI from denaturation under conditions of heat stress and oxidative stress.
血红素调节的真核起始因子2α激酶(HRI)不仅在血红素缺乏的兔网织红细胞裂解物(RRL)中被激活,而且在经热休克、N-乙基马来酰亚胺(MalNEt)或重金属离子处理的补充血红素的RRL中也被激活。我们之前已经证明,热休克蛋白Hsp90、Hsp70和FKBP52在RRL中与HRI相关;血红素可增强HRI与Hsp90和FKBP52的结合,但不增强与Hsp70的结合。为了研究Hsp90及其相关伴侣蛋白在HRI调节中的作用,我们检测了在补充血红素的RRL中,在热应激或氧化应激期间这些蛋白与HRI的相互作用。在经热、MalNEt或Hg2(+)处理的补充血红素的RRL中,HRI与Hsp90、FKBP52和p23的结合得以维持。甘油梯度离心和Sephacryl S-300凝胶过滤表明,热休克和MalNEt处理均不影响补充血红素的RRL中HRI的表观分子量。此外,活性HRI可与来自血红素缺乏和经MalNEt处理的补充血红素的RRL中的8D3抗Hsp90共同免疫沉淀。这些结果表明,HRI在热应激和氧化应激反应中的激活不需要Hsp90与HRI解离。此外,向Hsp90缺失的血红素缺乏的RRL中添加血红素会抑制HRI活性,这表明血红素对HRI活性的抑制不是由Hsp90与HRI的重新结合介导的。我们还检测了Hsp90与HRI相互作用的动力学。温度升高可刺激Hsp90与HRI相互作用的重建,且这需要Mg2+和ATP。向经MalNEt处理以使其伴侣蛋白复性能力失活的补充血红素的RRL中添加纯化的Hsp90,可保护HRI在41℃孵育时不发生不可逆的变性和聚集。我们的结果表明,Hsp90主要以分子伴侣的能力与HRI相互作用,在热应激和氧化应激条件下稳定HRI不发生变性。