Estus S, Golde T E, Kunishita T, Blades D, Lowery D, Eisen M, Usiak M, Qu X M, Tabira T, Greenberg B D
Division of Neuropathology, Case Western Reserve University, Cleveland, OH 44106.
Science. 1992 Feb 7;255(5045):726-8. doi: 10.1126/science.1738846.
The 39- to 43-amino acid amyloid beta protein (beta AP), which is deposited as amyloid in Alzheimer's disease, is encoded as an internal peptide that begins 99 residues from the carboxyl terminus of a 695- to 770-amino acid glycoprotein referred to as the amyloid beta protein precursor (beta APP). To clarify the processing that produces amyloid, carboxyl-terminal derivatives of the beta APP were analyzed. This analysis showed that the beta APP is normally processed into a complex set of 8- to 12-kilodalton carboxyl-terminal derivatives. The two largest derivatives in human brain have the entire beta AP at or near their amino terminus and are likely to be intermediates in the pathway leading to amyloid deposition.
由39至43个氨基酸组成的β淀粉样蛋白(β-AP)会在阿尔茨海默病中以淀粉样蛋白的形式沉积,它被编码为一种内部肽段,起始于一种名为β淀粉样蛋白前体(β-APP)的695至770个氨基酸糖蛋白羧基末端的99个残基处。为了阐明产生淀粉样蛋白的加工过程,对β-APP的羧基末端衍生物进行了分析。该分析表明,β-APP通常会被加工成一组复杂的8至12千道尔顿的羧基末端衍生物。人脑中两种最大的衍生物在其氨基末端或附近含有完整的β-AP,它们可能是导致淀粉样蛋白沉积途径中的中间体。