Sysmex Corporation, 4-4-4 Takatsukadai, Nishi-ku, Kobe 651-2271, Japan.
Bioinformatics Institute (BII), Agency for Science, Technology and Research (A*STAR), 30 Biopolis Street, 07-01, Matrix, Singapore 138671.
Trends Pharmacol Sci. 2018 Jan;39(1):49-58. doi: 10.1016/j.tips.2017.10.008. Epub 2017 Nov 10.
After decades of research and clinical trials there is still no cure for Alzheimer's disease (AD). While impaired clearance of amyloid beta (Aβ) peptides is considered as one of the major causes of AD, it was recently complemented by a potential role of other toxic amyloidogenic species. Insulin-degrading enzyme (IDE) is the proteolytic culprit of various β-forming peptides, both extracellular and intracellular. On the basis of demonstrated allosteric activation of IDE against Aβ, it is possible to propose a new strategy for the targeted IDE-based cleansing of different toxic aggregation-prone peptides. Consequently, specific allosteric activation of IDE coupled with state-of-the-art compound delivery and CRISP-Cas9 technique of transgene insertion can be instrumental in the fight against AD and related neurodegenerative maladies.
经过几十年的研究和临床试验,仍然没有治愈阿尔茨海默病(AD)的方法。虽然清除淀粉样β(Aβ)肽的能力受损被认为是 AD 的主要原因之一,但最近认为其他有毒的淀粉样蛋白物种也可能发挥作用。胰岛素降解酶(IDE)是各种β形成肽的蛋白水解罪魁祸首,包括细胞外和细胞内的肽。基于 IDE 对 Aβ 的变构激活的证明,针对不同的有毒聚集倾向肽,提出了一种基于 IDE 的靶向清除的新策略是有可能的。因此,与最先进的化合物传递相结合,特异性变构激活 IDE 以及 CRISP-Cas9 转基因插入技术,对于对抗 AD 和相关神经退行性疾病具有重要意义。