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 |
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Format: | Artikel |
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. |
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ISSN: | 0036-8075 1095-9203 |
DOI: | 10.1126/science.1738847 |