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Biochemistry. 2009 Dec 8;48(48):11329-31. doi: 10.1021/bi901325g.

A peptide hairpin inhibitor of amyloid beta-protein oligomerization and fibrillogenesis.

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  • 1Medical Scientist Training Program, David Geffen School of Medicineat UCLA, USA.

Abstract

Amyloid beta-protein (Abeta) self-assembly is linked strongly to Alzheimer's disease. We found that PP-Leu, a tridecapeptide analogue of broad-spectrum antiviral peptides termed theta-defensins, potently inhibits Abeta oligomer and fibril formation. This effect appeared to be mediated through sequestration of the amyloidogenic Abeta peptide in colloid-like assemblies. PP-Leu comprises a turn formed by a d-Pro-l-Pro amino acid dyad and stabilized by a disulfide bond, a motif that was exceptionally resistant to endoproteinase K digestion. This combination of assembly inhibitory activity and protease resistance suggests that PP-Leu may have potential therapeutic value.

PMID:
19877710
[PubMed - indexed for MEDLINE]
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