Presenilin endoproteolysis mediated by an aspartyl protease activity pharmacologically distinct from γ-secretase

William A. Campbell, Megan L.O. Reed, Jennifer Strahle, Michael S. Wolfe, Weiming Xia

Research output: Contribution to journalArticlepeer-review

43 Scopus citations


Presenilin (PS)-dependent γ-secretase cleavage is the final proteolytic step in generating amyloid β protein (Aβ), a key peptide involved in the pathogenesis of Alzheimer's disease. PS undergoes endoproteolysis by an unidentified 'presenilinase' to generate the functional N-terminal and C-terminal fragment heterodimers (NTF/CTF) that may harbor the γ-secretase active site. To better understand the relationship between presenilinase and γ-secretase, we characterized the biochemical properties of presenilinase and compared them with those of γ-secretase. Similar to γ-secretase, presenilinase was most active at acidic pH 6.3. Aspartyl protease inhibitor pepstatin A blocked presenilinase activity with an IC50 of ∼ 1 μM. Difluoroketone aspartyl protease transition state analogue MW167 was relatively selective for presenilinase (IC50 < 1 μM) over γ-secretase (IC50-16 μM). Importantly, removing the transition state mimicking moiety simultaneously abolished both presenilinase and γ-secretase inhibition, suggesting that presenilinase, like γ-secretase, is an aspartyl protease. Interestingly, several of the most potent γ-secretase inhibitors (IC50 = 0.3 or 20 nM) failed to block presenilinase activity. Although de novo generation of PS1 fragments coincided with production of Aβ in vitro, blocking presenilinase activity without reducing pre-existing fragment levels permitted normal de novo generation of Aβ and amyloid intracellular domain. Therefore, presenilinase has characteristics of an aspartyl protease, but this activity is distinct from γ-secretase.

Original languageEnglish (US)
Pages (from-to)1563-1574
Number of pages12
JournalJournal of Neurochemistry
Issue number6
StatePublished - Jun 2003


  • γ-secretase
  • Amyloid
  • Presenilin
  • Presenilinase

ASJC Scopus subject areas

  • Biochemistry
  • Cellular and Molecular Neuroscience


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