TY - JOUR
T1 - Potentially amyloidogenic, carboxyl-terminal derivatives of the amyloid protein precursor
AU - Estus, Steven
AU - Golde, Todd E.
AU - Kunishita, Tatsuhide
AU - Blades, Deborah
AU - Lowery, David
AU - Eisen, Matthew
AU - Usiak, Marianne
AU - Qu, Xuemei
AU - Tabira, Takeshi
AU - Greenberg, Barry D.
AU - Younkin, Steven G.
PY - 1992
Y1 - 1992
N2 - 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 carbozyl 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.
AB - 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 carbozyl 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.
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U2 - 10.1126/science.1738846
DO - 10.1126/science.1738846
M3 - Article
C2 - 1738846
AN - SCOPUS:0026522375
VL - 255
SP - 726
EP - 728
IS - 5045
ER -