Lihi Adler-Abramovich
Controlling the physical dimensions of peptide nanotubes by supramolecular polymer coassembly
Adler-Abramovich, Lihi; Marco, Pini; Arnon, Zohar A.; Creasey, Rhiannon C.G.; Michaels, Thomas C.T.; Levin, Aviad; Scurr, David J.; Roberts, Clive J.; Knowles, Tuomas P.J.; Tendler, Saul J.B.; Gazit, Ehud
Authors
Pini Marco
Zohar A. Arnon
Rhiannon C.G. Creasey
Thomas C.T. Michaels
Aviad Levin
Dr DAVID SCURR DAVID.SCURR@NOTTINGHAM.AC.UK
PRINCIPAL RESEARCH FELLOW
Professor CLIVE ROBERTS CLIVE.ROBERTS@NOTTINGHAM.AC.UK
HEAD OF SCHOOL - LIFE SCIENCES
Tuomas P.J. Knowles
Saul J.B. Tendler
Ehud Gazit
Abstract
Molecular self-assembly of peptides into ordered nanotubes is highly important for various technological applications. Very short peptide building blocks, as short as dipeptides, can form assemblies with unique mechanical, optical, piezoelectric, and semiconductive properties. Yet, the control over nanotube length in solution has remained challenging, due to the inherent sequential self-assembly mechanism. Here, in line with polymer chemistry paradigms, we applied a supramolecular polymer coassembly methodology to modulate peptide nanotube elongation. Utilizing this approach, we achieved a narrow, controllable nanotube length distribution by adjusting the molecular ratio of the diphenylalanine assembly unit and its end-capped analogue. Kinetic analysis suggested a slower coassembly organization process as compared to the self-assembly dynamics of each of the building blocks separately. This is consistent with a hierarchal arrangement of the peptide moieties within the coassemblies. Mass spectrometry analysis demonstrated the bimolecular composition of the coassembled nanostructures. Moreover, the peptide nanotubes’ length distribution, as determined by electron microscopy, was shown to fit a fragmentation kinetics model. Our results reveal a simple and efficient mechanism for the control of nanotube sizes through the coassembly of peptide entities at various ratios, allowing for the desired end-product formation. This dynamic size control offers tools for molecular engineering at the nanoscale exploiting the advantages of molecular coassembly.
Citation
Adler-Abramovich, L., Marco, P., Arnon, Z. A., Creasey, R. C., Michaels, T. C., Levin, A., Scurr, D. J., Roberts, C. J., Knowles, T. P., Tendler, S. J., & Gazit, E. (2016). Controlling the physical dimensions of peptide nanotubes by supramolecular polymer coassembly. ACS Nano, 10(8), 7436-7442. https://doi.org/10.1021/acsnano.6b01587
Journal Article Type | Article |
---|---|
Acceptance Date | Jun 28, 2016 |
Online Publication Date | Jul 28, 2016 |
Publication Date | Jun 28, 2016 |
Deposit Date | Nov 2, 2018 |
Journal | ACS Nano |
Print ISSN | 1936-0851 |
Electronic ISSN | 1936-086X |
Publisher | American Chemical Society |
Peer Reviewed | Peer Reviewed |
Volume | 10 |
Issue | 8 |
Pages | 7436-7442 |
DOI | https://doi.org/10.1021/acsnano.6b01587 |
Keywords | coassembly; diphenylalanine; peptide nanotubes; self-assembly; supramolecular polymers |
Public URL | https://nottingham-repository.worktribe.com/output/1219464 |
Publisher URL | https://pubs.acs.org/doi/10.1021/acsnano.6b01587 |
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