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Ultrasound-induced modulations of tetrapeptide hierarchical 1-D self-assembly and underlying molecular structures via sonocrystallization
Ultrasound was observed to modulate either underlying molecular structures or morphologies of tetrapeptide self-assembly from microtapes into nanotapes, nanofibers, and then nanorods with a different period of sonication. Herein, we report the ultrasound-induced modulations of the morphologies and u...
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Published in: | Journal of colloid and interface science 2009-09, Vol.337 (1), p.54-60 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Ultrasound was observed to modulate either underlying molecular structures or morphologies of tetrapeptide self-assembly from microtapes into nanotapes, nanofibers, and then nanorods with a different period of sonication.
Herein, we report the ultrasound-induced modulations of the morphologies and underlying molecular structures of tetrapeptide 1-D self-assembly. The self-assembly of the tetrapeptide (TTR108–111) precipitating out of the 1:1 mixed methanol/water is modulated from microtapes into nanotapes, nanofibers, and then bundles of nanorods when subjected to sonication for a period. The sonication-treated and untreated self-assemblies all give a set of equatorial pattern and a series of meridional pattern, indications of a typical “cross-β-structure” as the core structural motif. FTIR data indicate that all the assemblies contain a mixed pattern of β-sheets (dominant) and unstructured conformations (minor), and the relative proportion of unbound structures to β-sheets is as a function of sonication time, suggesting an ultrasound-induced modulation of β-sheet interactions. Accordingly, a possible model regarding a dynamic equilibrium between re-dissolution and re-assembling processes, e.g., a typical sonocrystallization process was proposed for such ultrasound-induced modulations of morphologies and underlying molecular structures. |
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ISSN: | 0021-9797 1095-7103 |
DOI: | 10.1016/j.jcis.2009.05.024 |