MagicWand: A Single, Designed Peptide That Assembles to Stable, Ordered α-Helical Fibers

• Published in: Biochemistry (Easton) Vol. 47; no. 39; pp. 10365 - 10371
• Main Authors: Gribbon, Christopher, Channon, Kevin J, Zhang, Weijie, Banwell, Eleanor F, Bromley, Elizabeth H. C, Chaudhuri, Julian B, Oreffo, Richard O. C, Woolfson, Derek N
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 30.09.2008
• Subjects: Amino Acid Motifs; Amino Acid Sequence; Circular Dichroism; Microscopy, Electron; Models, Molecular; Peptides - chemical synthesis; Peptides - chemistry; Protein Conformation; Protein Denaturation; Protein Structure, Secondary; Protein Structure, Tertiary; Spectrophotometry
• ISSN: 0006-2960; 1520-4995
• DOI: 10.1021/bi801072s

We describe a straightforward single-peptide design that self-assembles into extended and thickened nano-to-mesoscale fibers of remarkable stability and order. The basic chassis of the design is the well-understood dimeric α-helical coiled-coil motif. As such, the peptide has a heptad sequence repeat, abcdefg , with isoleucine and leucine residues at the a and d sites to ensure dimerization. In addition, to direct staggered assembly of peptides and to foster fibrillogenesisthat is, as opposed to blunt-ended discrete speciesthe terminal quarters of the peptide are cationic and the central half anionic with lysine and glutamate, respectively, at core-flanking e and g positions. This +,−,−,+ arrangement gives the peptide its name, MagicWand (MW). As judged by circular dichroism (CD) spectra, MW assembles to α-helical structures in the sub-micromolar range and above. The thermal unfolding of MW is reversible with a melting temperature >70 °C at 100 μM peptide concentration. Negative-stain transmission electron microscopy (TEM) of MW assemblies reveals stiff, straight, fibrous rods that extended for tens of microns. Moreover, different stains highlight considerable order both perpendicular and parallel to the fiber long axis. The dimensions of these features are consistent with bundles of long, straight coiled α-helical coiled coils with their axes aligned parallel to the long axis of the fibers. The fiber thickening indicates inter-coiled-coil interactions. Mutagenesis of the outer surface of the peptidei.e., at the b and f positionscombined with stability and microscopy measurements, highlights the role of electrostatic and cation−π interactions in driving fiber formation, stability and thickening. These findings are discussed in the context of the growing number of self-assembling peptide-based fibrous systems.