Out-of-register β-sheets suggest a pathway to toxic amyloid aggregates.

Publication Type:

Journal Article


Proc Natl Acad Sci U S A, Volume 109, Issue 51, p.20913-8 (2012)


Amyloid, beta 2-Microglobulin, Congo Red, Crystallography, X-Ray, Fluorescent Dyes, Humans, Hydrogen Bonding, Microscopy, Electron, Transmission, Models, Molecular, Molecular Conformation, Peptides, Protein Conformation, Protein Structure, Secondary, Proteins, Thermodynamics, X-Ray Diffraction


<p>Although aberrant protein aggregation has been conclusively linked to dozens of devastating amyloid diseases, scientists remain puzzled about the molecular features that render amyloid fibrils or small oligomers toxic. Here, we report a previously unobserved type of amyloid fibril that tests as cytotoxic: one in which the strands of the contributing β-sheets are out of register. In all amyloid fibrils previously characterized at the molecular level, only in-register β-sheets have been observed, in which each strand makes its full complement of hydrogen bonds with the strands above and below it in the fibril. In out-of-register sheets, strands are sheared relative to one another, leaving dangling hydrogen bonds. Based on this finding, we designed out-of-register β-sheet amyloid mimics, which form both cylindrin-like oligomers and fibrils, and these mimics are cytotoxic. Structural and energetic considerations suggest that out-of-register fibrils can readily convert to toxic cylindrins. We propose that out-of-register β-sheets and their related cylindrins are part of a toxic amyloid pathway, which is distinct from the more energetically favored in-register amyloid pathway.</p>