期刊
ISRAEL JOURNAL OF CHEMISTRY
卷 54, 期 5-6, 页码 703-707出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/ijch.201400025
关键词
amino acids; amyloid beta-peptides; bioelectronics; heterocycles; self-assembly
资金
- ISF [1293/08]
- Kreitman Fellowship for doctoral research
- Israel Ministry of Science, Technology and Space Scholarship for Women in the Fields of Exact Sciences and Engineering
The incorporation of non-canonical amino acids with aromatic side chains is considered to be a promising way to improve and control the electronic properties of self-assembled peptide nanostructures. In this work, we have studied the influence of aromatic ring heteroatom on the electronic properties of amyloid beta-derived peptide fiber networks. We show that the incorporation of furan instead of thiophene side chains results in only small changes in the resistivity of the peptide network, with a threefold increase in the sheet resistance and a small decrease in the contact resistance. These changes can be explained by a twofold decrease in the diameter of the self-assembled fibers. These characteristics open the way to the use of furan-instead of thiophene-based analogues as non-natural side-chain modifications of peptides for electronic applications; this makes the fibrils more biodegradable and biorenewable.
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