Chiral Selectivity of Secondary Nucleation in Amyloid Fibril Propagation. Issue 45 (5th October 2021)

• Record Type: Journal Article
• Authors: Törnquist, Mattias; Linse, Sara
• Is Part Of: Angewandte Chemie international edition. Volume 60:Issue 45(2021)
• Page Start: 24008
• Page End: 24011
• Publication Date: 2021-10-05
• Subjects: aggregation -- amyloid-beta peptides -- autocatalysis -- enantioselectivity -- secondary nucleation; Chemistry -- Periodicals; 540
• DOI: 10.1002/anie.202108648
• Languages: English
• ISSNs: 1433-7851

Abstract

Abstract: Chirality is a fundamental feature of asymmetric molecules and of critical importance for intermolecular interactions. The growth of amyloid fibrils displays a strong enantioselectivity, which is manifested as elongation through the addition of monomers of the same, but not opposite, chirality as the parent aggregate. Here we ask whether also secondary nucleation on the surface of amyloid fibrils, of relevance for toxicity, is governed by the chirality of the nucleating monomers. We use short amyloid peptides (Aβ20‐34 and IAPP20‐29) with all residues as L‐ or all D‐enantiomer in self and cross‐seeding experiments with low enough seed concentration that any acceleration of fibril formation is dominated by secondary nucleation. We find a strong enantio‐specificity of this auto‐catalytic process with secondary nucleation being observed in the self‐seeding experiments only. The results highlight a role of secondary nucleation in strain propagation. Abstract : Amyloid‐forming peptides are chiral substances. While the growth of amyloid fibrils is known to be enantiospecific, we show here that this applies also to secondary nucleation of monomers in the presence of fibrils. Secondary nucleation is only possible if the monomers in solution and aggregate are of the same chirality.