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Assembly pathway of a designed alpha-helical protein fiber
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Bromley, Elizabeth H. C., Channon, Kevin J., King, Patrick J. S., Mahmoud, Zahra N., Banwell, Eleanor F., Butler, M. F. (Michael F.), Crump, Matthew P., Dafforn, Tim, Hicks, Matthew R., Hirst, Jonathan D., Rodger, Alison and Woolfson, Derek N. (2010) Assembly pathway of a designed alpha-helical protein fiber. Biophysical Journal, Vol.98 (No.8). pp. 1668-1676. doi:10.1016/j.bpj.2009.12.4309 ISSN 0006-3495.
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Official URL: http://dx.doi.org/10.1016/j.bpj.2009.12.4309
Abstract
Interest in the design of peptide-based fibrous materials is growing because it opens possibilities to explore fundamental aspects of peptide self-assembly and to exploit the resulting structures for example, as scaffolds for tissue engineering. Here we investigate the assembly pathway of self-assembling fibers, a rationally designed a-helical coiled-coil system comprising two peptides that assemble on mixing. The dimensions spanned by the peptides and final structures (nanometers to micrometers), and the timescale over which folding and assembly occur (seconds to hours), necessitate a multi-technique approach employing spectroscopy, analytical ultracentrifugation, electron and light microscopy, and protein design to produce a physical model. We show that fibers form via a nucleation and growth mechanism. The two peptides combine rapidly (in less than seconds) to form sticky ended, partly helical heterodimers. A lag phase follows, on the order of tens of minutes, and is concentration-dependent. The critical nucleus comprises six to eight partially folded dimers. Growth is then linear in dimers, and subsequent fiber growth occurs in hours through both elongation and thickening. At later times (several hours), fibers grow predominantly through elongation. This kinetic, biomolecular description of the folding-and-assembly process allows the self-assembling fiber system to be manipulated and controlled, which we demonstrate through seeding experiments to obtain different distributions of fiber lengths. This study and the resulting mechanism we propose provide a potential route to achieving temporal control of functional fibers with future applications in biotechnology and nanoscale science and technology.
Item Type: | Journal Article | ||||
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Subjects: | Q Science > QD Chemistry T Technology > TP Chemical technology |
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Divisions: | Faculty of Science, Engineering and Medicine > Science > Chemistry | ||||
Library of Congress Subject Headings (LCSH): | Peptides, Self-assembly (Chemistry), Fibers, Proteins, Protein engineering | ||||
Journal or Publication Title: | Biophysical Journal | ||||
Publisher: | Biophysical Society | ||||
ISSN: | 0006-3495 | ||||
Official Date: | 21 April 2010 | ||||
Dates: |
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Volume: | Vol.98 | ||||
Number: | No.8 | ||||
Number of Pages: | 9 | ||||
Page Range: | pp. 1668-1676 | ||||
DOI: | 10.1016/j.bpj.2009.12.4309 | ||||
Status: | Peer Reviewed | ||||
Publication Status: | Published | ||||
Access rights to Published version: | Restricted or Subscription Access | ||||
Funder: | Engineering and Physical Sciences Research Council (EPSRC), Biotechnology and Biological Sciences Research Council (Great Britain) (BBSRC), Unilever Ltd., University of Bristol | ||||
Grant number: | GR/T09224 (EPSRC), E022359 (BBSRC) |
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