Hatahet Feras, Ruddock Lloyd W
Department of Biochemistry, Linnanmaa Campus, University of Oulu, 90570 Oulu, Finland.
Curr Pharm Des. 2009;15(21):2488-507. doi: 10.2174/138161209788682343.
Protein folding in the cell is a complex process with a fine balance between productive and non-productive folding. To modulate, either up-regulating or down-regulating, the level of one specific protein with multiple approaches is possible, including the modulation of catalysed protein folding, the use of chemical and pharmacological chaperones, alteration of natural protein-protein interactions, the regulation of degradative pathways and manipulation of natural control mechanisms, such as the heat shock response and the unfolded protein response. Errors in proteostasis are linked to a wide range of disease states and many examples exist of the successful manipulation of proteostasis for the partial or complete elimination of the disease phenotype, including for many amyloid based diseases such as Parkinson's and Alzheimer's as well as for 'loss-of-function' diseases such as Fabry's and Gaucher's diseases. This review takes an overview of the different approaches that can be used to alter proteostasis with an emphasis on peptidomimetic inhibitors and activators of protein folding. It covers the modulators available, their mechanisms of action and potential limitations, including the problems of specificity in altering proteostasis.
细胞内的蛋白质折叠是一个复杂的过程,在有效折叠和无效折叠之间保持着精细的平衡。通过多种方法调节(上调或下调)一种特定蛋白质的水平是可行的,这些方法包括调节催化性蛋白质折叠、使用化学和药理伴侣分子、改变天然的蛋白质-蛋白质相互作用、调节降解途径以及操纵天然控制机制,如热休克反应和未折叠蛋白反应。蛋白质稳态的错误与多种疾病状态相关,并且存在许多成功操纵蛋白质稳态以部分或完全消除疾病表型的例子,包括许多基于淀粉样蛋白的疾病,如帕金森病和阿尔茨海默病,以及“功能丧失”疾病,如法布里病和戈谢病。本综述概述了可用于改变蛋白质稳态的不同方法,重点是蛋白质折叠的拟肽抑制剂和激活剂。它涵盖了可用的调节剂、它们的作用机制和潜在局限性,包括改变蛋白质稳态时的特异性问题。