Asymmetric Peptide Nanoribbons
Author(s) -
Zhilin Yu,
Faifan Tantakitti,
Liam C. Palmer,
Samuel I. Stupp
Publication year - 2016
Publication title -
nano letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.853
H-Index - 488
eISSN - 1530-6992
pISSN - 1530-6984
DOI - 10.1021/acs.nanolett.6b03062
Subject(s) - supramolecular chemistry , self assembly , nanotechnology , nanostructure , non covalent interactions , asymmetry , nanoparticle , chemistry , peptide , nanoscopic scale , supramolecular polymers , colloidal gold , supramolecular assembly , materials science , chemical physics , crystallography , molecule , physics , hydrogen bond , crystal structure , organic chemistry , quantum mechanics , biochemistry
Asymmetry in chemical structure or shape at molecular, nanoscale, or microscopic levels is essential to a vast number of functionalities in both natural and artificial systems. Bottom-up approaches to create asymmetric supramolecular nanostructures are considered promising but this strategy suffers from the potentially dynamic nature of noncovalent interactions. We report here on supramolecular self-assembly of asymmetric peptide amphiphiles consisting of two different molecularly linked domains. We found that strong noncovalent interactions and a high degree of internal order among the asymmetric amphiphiles lead to nanoribbons with asymmetric faces due to the preferential self-association of the two domains. The capture of gold nanoparticles on only one face of the nanoribbons demonstrates symmetry breaking in these supramolecular structures.
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