Abstract

The 39- to 43-amino acid amyloid β protein (βAP), 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 β protein precursor (βAPP). To clarify the processing that produces amyloid, carboxyl-terminal derivatives of the βAPP were analyzed. This analysis showed that the βAPP 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 βAP at or near their amino terminus and are likely to be intermediates in the pathway leading to amyloid deposition.

Keywords

Amyloid precursor proteinP3 peptideAmyloid (mycology)PeptideChemistryBiochemistryAmino acidBETA (programming language)Biochemistry of Alzheimer's diseaseProtein precursorAmyloid betaGlycoproteinPeptide sequenceN-terminusC-terminusAlzheimer's diseaseEnzymeMedicineDiseaseInternal medicine

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Publication Info

Year
1992
Type
article
Volume
255
Issue
5045
Pages
726-728
Citations
433
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Closed

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Steven Estus, Todd E. Golde, Tatsuhide Kunishita et al. (1992). Potentially Amyloidogenic, Carboxyl-Terminal Derivatives of the Amyloid Protein Precursor. Science , 255 (5045) , 726-728. https://doi.org/10.1126/science.1738846

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DOI
10.1126/science.1738846