Lleó Alberto, Berezovska Oksana, Herl Lauren, Raju Susan, Deng Amy, Bacskai Brian J, Frosch Matthew P, Irizarry Michael, Hyman Bradley T
Alzheimer Research Unit, Massachusetts General Hospital, 114 16th St, Charlestown, Massachusetts 02129, USA.
Nat Med. 2004 Oct;10(10):1065-6. doi: 10.1038/nm1112. Epub 2004 Sep 26.
Recent reports suggest that some commonly used nonsteroidal anti-inflammatory drugs (NSAIDs) unexpectedly shift the cleavage products of amyloid precursor protein (APP) to shorter, less fibrillogenic forms, although the underlying mechanism remains unknown. We now demonstrate, using a fluorescence resonance energy transfer method, that Abeta(42)-lowering NSAIDs specifically affect the proximity between APP and presenilin 1 and alter presenilin 1 conformation both in vitro and in vivo, suggesting a novel allosteric mechanism of action.
最近的报告表明,一些常用的非甾体抗炎药(NSAIDs)意外地将淀粉样前体蛋白(APP)的裂解产物转变为更短、更少形成纤维的形式,尽管其潜在机制尚不清楚。我们现在使用荧光共振能量转移方法证明,降低β淀粉样蛋白42(Aβ42)的NSAIDs在体外和体内均特异性地影响APP与早老素1之间的接近度,并改变早老素1的构象,提示一种新的变构作用机制。