Departments of Chemistry and Molecular and Experimental Medicine and The Skaggs Institute for Chemical Biology, The Scripps Research Institute, La Jolla, CA 92037, United States.
Curr Opin Cell Biol. 2011 Apr;23(2):231-8. doi: 10.1016/j.ceb.2010.11.002. Epub 2010 Dec 9.
Inheriting a mutant misfolding-prone protein that cannot be efficiently folded in a given cell type(s) results in a spectrum of human loss-of-function misfolding diseases. The inability of the biological protein maturation pathways to adapt to a specific misfolding-prone protein also contributes to pathology. Chemical and biological therapeutic strategies are presented that restore protein homeostasis, or proteostasis, either by enhancing the biological capacity of the proteostasis network or through small molecule stabilization of a specific misfolding-prone protein. Herein, we review the recent literature on therapeutic strategies to ameliorate protein misfolding diseases that function through either of these mechanisms, or a combination thereof, and provide our perspective on the promise of alleviating protein misfolding diseases by taking advantage of proteostasis adaptation.
遗传一种在特定细胞类型中不能有效折叠的突变错误折叠蛋白会导致一系列人类功能丧失性错误折叠疾病。生物蛋白成熟途径无法适应特定的错误折叠蛋白也会导致病理。本文提出了一些化学和生物治疗策略,通过增强蛋白质稳态网络的生物学能力,或通过小分子稳定特定的错误折叠蛋白,来恢复蛋白质的内稳态或蛋白质稳态。在此,我们综述了最近关于通过这些机制或其组合来改善蛋白质错误折叠疾病的治疗策略的文献,并就利用蛋白质稳态适应来缓解蛋白质错误折叠疾病的前景提供了我们的观点。