"Threading" of Β-sheet peptides via radical polymerization

Takeshi Mori; Shiro Yasutake; Hideki Inoue; Keiji Minagawa; Masami Tanaka; Takuro Niidome; Yoshiki Katayama

doi:10.1021/bm060835n

"Threading" of Β-sheet peptides via radical polymerization

Takeshi Mori, Shiro Yasutake, Hideki Inoue, Keiji Minagawa, Masami Tanaka, Takuro Niidome, Yoshiki Katayama

Research output: Contribution to journal › Article › peer-review

1 Citation (Scopus)

Abstract

A nonamer peptide containing a diene group in the center of the sequence was synthesized. When the peptide forms an antiparallel β-sheet, the diene groups align ca. 5 Å apart on the β-sheet. The diene groups successfully photopolymerized without distorting the β-sheet structure. The obtained β-sheet showed high stability against acid denaturation and addition of 1,1,1,3,3,3-hexafluoroisopropanol.

Original language	English
Pages (from-to)	318-321
Number of pages	4
Journal	Biomacromolecules
Volume	8
Issue number	2
DOIs	https://doi.org/10.1021/bm060835n
Publication status	Published - Feb 1 2007

All Science Journal Classification (ASJC) codes

Bioengineering
Biomaterials
Polymers and Plastics
Materials Chemistry

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10.1021/bm060835n

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abstract = "A nonamer peptide containing a diene group in the center of the sequence was synthesized. When the peptide forms an antiparallel β-sheet, the diene groups align ca. 5 {\AA} apart on the β-sheet. The diene groups successfully photopolymerized without distorting the β-sheet structure. The obtained β-sheet showed high stability against acid denaturation and addition of 1,1,1,3,3,3-hexafluoroisopropanol.",

author = "Takeshi Mori and Shiro Yasutake and Hideki Inoue and Keiji Minagawa and Masami Tanaka and Takuro Niidome and Yoshiki Katayama",

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T1 - "Threading" of Β-sheet peptides via radical polymerization

AU - Mori, Takeshi

AU - Yasutake, Shiro

AU - Inoue, Hideki

AU - Minagawa, Keiji

AU - Tanaka, Masami

AU - Niidome, Takuro

AU - Katayama, Yoshiki

PY - 2007/2/1

Y1 - 2007/2/1

N2 - A nonamer peptide containing a diene group in the center of the sequence was synthesized. When the peptide forms an antiparallel β-sheet, the diene groups align ca. 5 Å apart on the β-sheet. The diene groups successfully photopolymerized without distorting the β-sheet structure. The obtained β-sheet showed high stability against acid denaturation and addition of 1,1,1,3,3,3-hexafluoroisopropanol.

AB - A nonamer peptide containing a diene group in the center of the sequence was synthesized. When the peptide forms an antiparallel β-sheet, the diene groups align ca. 5 Å apart on the β-sheet. The diene groups successfully photopolymerized without distorting the β-sheet structure. The obtained β-sheet showed high stability against acid denaturation and addition of 1,1,1,3,3,3-hexafluoroisopropanol.

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JO - Biomacromolecules

JF - Biomacromolecules

IS - 2

ER -

"Threading" of Β-sheet peptides via radical polymerization

Abstract

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