Ray, Sudipta ; Haldar, Debasish ; Drew, Michael G. B. ; Banerjee, Arindam (2004) A new motif in the formation of peptide nanotubes: the crystallographic signature Organic Letters, 6 (24). pp. 4463-4465. ISSN 1523-7060
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Official URL: http://pubs.acs.org/doi/abs/10.1021/ol048253a
Related URL: http://dx.doi.org/10.1021/ol048253a
Abstract
Terminally protected acyclic tripeptides Boc-Tyr(1)-Val(2)-Tyr(3)-OMe 1 and Boc-Tyr(1)-lle(2)-Tyr(3)-OMe 2 self-assemble into nanotubes in crystals through various noncovalent interactions with an average internal diameter of 5 Angstrom (0.5 nm), and the tubular ensemble is developed through the hydrogen-bonded side chains of tyrosine residues. The inside of the hollow nanotubular structures is hydrophilic; however, no solvent molecules have been crystallographically detected.
Item Type: | Article |
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Source: | Copyright of this article belongs to American Chemical Society. |
Keywords: | Assembling Prganic Nanotubes; Helical Rosette Nanotubes; Cyclic-Peptides; Design |
ID Code: | 99530 |
Deposited On: | 07 Nov 2016 11:37 |
Last Modified: | 07 Nov 2016 11:37 |
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