1. A Cyclic Peptide Inhibitor of ApoC-II Peptide Fibril Formation: Mechanistic Insight from NMR and Molecular Dynamics Analysis
- Author
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Griffin, Michael D.W., Yeung, Levi, Hung, Andrew, Todorova, Nevena, Mok, Yee-Foong, Karas, John A., Gooley, Paul R., Yarovsky, Irene, and Howlett, Geoffrey J.
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NUCLEAR magnetic resonance , *MOLECULAR dynamics , *APOLIPOPROTEINS , *DISULFIDES , *THIOFLAVINS , *MOLECULAR weights - Abstract
Abstract: The misfolding and aggregation of proteins to form amyloid fibrils is a characteristic feature of several common age-related diseases. Agents that directly inhibit formation of amyloid fibrils represent one approach to combating these diseases. We have investigated the potential of a cyclic peptide to inhibit fibril formation by fibrillogenic peptides from human apolipoprotein C-II (apoC-II). Cyc[60–70] was formed by disulfide cross-linking of cysteine residues added to the termini of the fibrillogenic peptide comprising apoC-II residues 60–70. This cyclic peptide did not self-associate into fibrils. However, substoichiometric concentrations of cyc[60–70] significantly delayed fibril formation by the fibrillogenic, linear peptides apoC-II[60–70] and apoC-II[56–76]. Reduction of the disulfide bond or scrambling the amino acid sequence within cyc[60–70] significantly impaired its inhibitory activity. The solution structure of cyc[60–70] was solved using NMR spectroscopy, revealing a well-defined structure comprising a hydrophilic face and a more hydrophobic face containing the Met60, Tyr63, Ile66 and Phe67 side chains. Molecular dynamics (MD) studies identified a flexible central region within cyc[60–70], while MD simulations of “scrambled” cyc[60–70] indicated an increased formation of intramolecular hydrogen bonds and a reduction in the overall flexibility of the peptide. Our structural studies suggest that the inhibitory activity of cyc[60–70] is mediated by an elongated structure with inherent flexibility and distinct hydrophobic and hydrophilic faces, enabling cyc[60–70] to interact transiently with fibrillogenic peptides and inhibit fibril assembly. These results suggest that cyclic peptides based on amyloidogenic core peptides could be useful as specific inhibitors of amyloid fibril formation. [Copyright &y& Elsevier]
- Published
- 2012
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