Issue 31, 2012

Fibrillisation of ring-closed amyloid peptides

Abstract

Ring-closing olefin metathesis reactions are used to create intra-molecularly ring closed peptides or inter-molecularly ring-closed peptide dimers based on a designed amyloid peptide sequence. The uncrosslinked peptide self-assembles into high aspect ratio nanotubes, however ring-closing leads to the formation of fibrillar and twisted/helical ribbon structures.

Graphical abstract: Fibrillisation of ring-closed amyloid peptides

Supplementary files

Article information

Article type
Communication
Submitted
05 Dec 2011
Accepted
21 Feb 2012
First published
22 Feb 2012

Chem. Commun., 2012,48, 3757-3759

Fibrillisation of ring-closed amyloid peptides

I. W. Hamley, G. Cheng, V. Castelletto, S. Handschin and R. Mezzenga, Chem. Commun., 2012, 48, 3757 DOI: 10.1039/C2CC17583E

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements