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Isolation of functionally active gamma- secretase protein complex and methods for detection of activity and Inhibitors thereof

机译:具有功能活性的γ-分泌酶蛋白复合物的分离及其活性检测方法和抑制剂

摘要

The present invention provides an isolated, functionally-active protein that catalyzes cleavage of a gamma-secretase substrate. The functional activity of the isolated protein suggests that the isolated protein includes gamma-secretase. In one embodiment, the isolated gamma-secretase protein is associated with PS1. The present invention also relates to homogeneous methods for monitoring cleavage of &bgr;-amyloid precursor protein (&bgr;APP) by gamma-secretase, wherein the steps of of isolating and retrieving cleavage products have been eliminated. Cleavage can be detected by binding a pair of fluorescent adducts to the gamma-cleaved &bgr;APP fragment. Preferably, a first fluorescent adduct binds to the carboxy-terminal end of the gamma-cleaved &bgr;APP fragment, with substantially no cross-reactivity to uncleaved &bgr;APP or to other types of gamma-cleaved &bgr;APP fragments, while a second fluorescent adduct binds to a portion within the amino-terminal region on the gamma-cleaved &bgr;APP fragment. Detection of binding to the gamma-cleaved &bgr;APP fragment is determined by monitoring the fluorescent energy transfer between the adducts.
机译:本发明提供了分离的,具有功能活性的蛋白质,其催化γ-分泌酶底物的裂解。分离的蛋白质的功能活性表明分离的蛋白质包括γ-分泌酶。在一个实施方案中,分离的γ-分泌酶蛋白与PS1相关。本发明还涉及通过γ-分泌酶监测β-淀粉样前体蛋白(βAPP)的切割的均质方法,其中省去了分离和回收切割产物的步骤。裂解可以通过将一对荧光加合物结合到γ裂解的APP片段上来检测。优选地,第一荧光加合物结合至γ-裂解的APP片段的羧基末端,而与未裂解的APP或其他类型的γ裂解的APP片段基本上没有交叉反应,而第二种荧光加合物结合到γ切割的APP片段的氨基末端区域内的一部分上。通过监测加合物之间的荧光能量转移来确定与γ切割的APP片段结合的检测。

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