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Self-assembly and hydrogel formation ability of Fmoc-dipeptides comprising α-methyl-L-phenylalanine
Various biofunctional hydrogel materials can be fabricated in aqueous media through the self-assembly of peptide derivatives, forming supramolecular nanostructures and their three-dimensional networks. In this study, we describe the self-assembly of new Fmoc-dipeptides comprising α-methyl-L-phenylal...
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Published in: | Polymer journal 2020-08, Vol.52 (8), p.923-930 |
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creator | Arakawa, Hanae Takeda, Kumi Higashi, Sayuri L. Shibata, Aya Kitamura, Yoshiaki Ikeda, Masato |
description | Various biofunctional hydrogel materials can be fabricated in aqueous media through the self-assembly of peptide derivatives, forming supramolecular nanostructures and their three-dimensional networks. In this study, we describe the self-assembly of new Fmoc-dipeptides comprising α-methyl-L-phenylalanine. We found that the position and number of methyl groups introduced onto the α carbons of the Fmoc-dipeptides by α-methyl-L-phenylalanine have a marked influence on the morphology of the supramolecular nanostructure as well as the hydrogel (network) formation ability.
This article describes the self-assembly of Fmoc-dipeptides comprising α-methyl-L-phenylalanine. The position and number of methyl groups introduced onto the α carbons of the Fmoc-dipeptides as α-methyl-L-phenylalanine have a marked influence on the morphology of supramolecular nanostructures and the hydrogel formation ability. |
doi_str_mv | 10.1038/s41428-019-0301-5 |
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This article describes the self-assembly of Fmoc-dipeptides comprising α-methyl-L-phenylalanine. The position and number of methyl groups introduced onto the α carbons of the Fmoc-dipeptides as α-methyl-L-phenylalanine have a marked influence on the morphology of supramolecular nanostructures and the hydrogel formation ability.</description><identifier>ISSN: 0032-3896</identifier><identifier>EISSN: 1349-0540</identifier><identifier>DOI: 10.1038/s41428-019-0301-5</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>639/301/54 ; 639/638/541 ; Aqueous solutions ; Biomaterials ; Bioorganic Chemistry ; Chemistry ; Chemistry and Materials Science ; Chemistry/Food Science ; Hydrogels ; Morphology ; Nanostructure ; Original Article ; Phenylalanine ; Polymer Sciences ; Self-assembly ; Surfaces and Interfaces ; Thin Films</subject><ispartof>Polymer journal, 2020-08, Vol.52 (8), p.923-930</ispartof><rights>The Author(s) 2020</rights><rights>The Author(s) 2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c359t-41302109457f0ff8eead9c3587301b66e15b7b46a0a5c19b2d2f3422155b78b3</citedby><cites>FETCH-LOGICAL-c359t-41302109457f0ff8eead9c3587301b66e15b7b46a0a5c19b2d2f3422155b78b3</cites><orcidid>0000-0003-4097-8292 ; 0000-0002-5785-6892</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Arakawa, Hanae</creatorcontrib><creatorcontrib>Takeda, Kumi</creatorcontrib><creatorcontrib>Higashi, Sayuri L.</creatorcontrib><creatorcontrib>Shibata, Aya</creatorcontrib><creatorcontrib>Kitamura, Yoshiaki</creatorcontrib><creatorcontrib>Ikeda, Masato</creatorcontrib><title>Self-assembly and hydrogel formation ability of Fmoc-dipeptides comprising α-methyl-L-phenylalanine</title><title>Polymer journal</title><addtitle>Polym J</addtitle><description>Various biofunctional hydrogel materials can be fabricated in aqueous media through the self-assembly of peptide derivatives, forming supramolecular nanostructures and their three-dimensional networks. In this study, we describe the self-assembly of new Fmoc-dipeptides comprising α-methyl-L-phenylalanine. We found that the position and number of methyl groups introduced onto the α carbons of the Fmoc-dipeptides by α-methyl-L-phenylalanine have a marked influence on the morphology of the supramolecular nanostructure as well as the hydrogel (network) formation ability.
This article describes the self-assembly of Fmoc-dipeptides comprising α-methyl-L-phenylalanine. 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subjects | 639/301/54 639/638/541 Aqueous solutions Biomaterials Bioorganic Chemistry Chemistry Chemistry and Materials Science Chemistry/Food Science Hydrogels Morphology Nanostructure Original Article Phenylalanine Polymer Sciences Self-assembly Surfaces and Interfaces Thin Films |
title | Self-assembly and hydrogel formation ability of Fmoc-dipeptides comprising α-methyl-L-phenylalanine |
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