Processing of the Amyloid Protein Precursor to Potentially Amyloidogenic Derivatives

The ∼120-kilodalton amyloid β protein precursor (β APP) is processed into a complex set of 8- to 12-kilodalton carboxyl-terminal derivatives that includes potentially amyloidogenic forms with the ∼4-kilodalton amyloid β protein (β AP) at or near their amino terminus. In order to determine if these d...

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Veröffentlicht in:Science (American Association for the Advancement of Science) 1992-02, Vol.255 (5045), p.728-730
Hauptverfasser: Golde, Todd E., Estus, Steven, Younkin, Linda H., Selkoe, Dennis J., Younkin, Steven G.
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Sprache:eng
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Zusammenfassung:The ∼120-kilodalton amyloid β protein precursor (β APP) is processed into a complex set of 8- to 12-kilodalton carboxyl-terminal derivatives that includes potentially amyloidogenic forms with the ∼4-kilodalton amyloid β protein (β AP) at or near their amino terminus. In order to determine if these derivatives are processed in a secretory pathway or by the endosomal-lysosomal system, (i) deletion mutants that produce the normal set of carboxyl-terminal derivatives and shortened secreted derivatives were analyzed and (ii) the effect of inhibitors of endosomal-lysosomal processing was examined. In the secretory pathway, cleavage of the β APP occurs at a single site within the β AP to generate one secreted derivative and one nonamyloidogenic carboxyl-terminal fragment, whereas, in the endosomal-lysosomal system, a complex set of carboxyl-terminal derivatives is produced that includes the potentially amyloidogenic forms.
ISSN:0036-8075
1095-9203
DOI:10.1126/science.1738847