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Two β-forms and the α-helix of N-octanoyl-L-glutamic acid oligomers
https://nitech.repo.nii.ac.jp/records/4121
https://nitech.repo.nii.ac.jp/records/412176ce7948-725c-4776-a096-293102df1d5a
名前 / ファイル | ライセンス | アクション |
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J. CHEM. SOC. FARADAY TRANS., 1992, 88(23), 3451-3459 -Reproduced by permission of The Royal Society of Chemistry (RSC)
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Item type | 学術雑誌論文 / Journal Article(1) | |||||
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公開日 | 2012-11-06 | |||||
タイトル | ||||||
言語 | en | |||||
タイトル | Two β-forms and the α-helix of N-octanoyl-L-glutamic acid oligomers | |||||
言語 | ||||||
言語 | eng | |||||
資源タイプ | ||||||
資源タイプ識別子 | http://purl.org/coar/resource_type/c_6501 | |||||
資源タイプ | journal article | |||||
著者 |
Uehara, Toshiyuki
× Uehara, Toshiyuki× Okabayashi, Hirofumi× Taga, Keijiro× Yoshida, Tadayoshi× Kojima, Hiroshi |
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著者別名 | ||||||
姓名 | 多賀, 圭次郎 | |||||
書誌情報 |
Journal of the Chemical Society. Faraday transactions. 巻 88, 号 23, p. 3451-3459, 発行日 1992-01-01 |
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出版者 | ||||||
出版者 | Royal Society of Chemistry | |||||
ISSN | ||||||
収録物識別子タイプ | ISSN | |||||
収録物識別子 | 09565000 | |||||
書誌レコードID(NCID) | ||||||
収録物識別子タイプ | NCID | |||||
収録物識別子 | AA10743481 | |||||
著者版フラグ | ||||||
出版タイプ | VoR | |||||
出版タイプResource | http://purl.org/coar/version/c_970fb48d4fbd8a85 | |||||
DOI | ||||||
関連タイプ | isIdenticalTo | |||||
識別子タイプ | DOI | |||||
関連識別子 | http://dx.doi.org/10.1039/FT9928803451 | |||||
関連名称 | 10.1039/FT9928803451 | |||||
内容記述 | ||||||
内容記述タイプ | Other | |||||
内容記述 | N-Octanoyl-L-glutamic acid oligomers (residue number, N = 3-6, 8, 10, 12, 14, 16, 18, 20 and 22) have been synthesized in order to study their molecular conformations in the solid state. The X-ray diffraction powder patterns and the vibrational spectra of these oligomers have been investigated and compared with those of two β-forms (β1 and β2) and the α-helix of poly(L-glutamic acid). The results are summarized as follows. These oligomers take up a β1- or β2-like structure, similar to that of the two β-forms of poly(L-glutamic acid). The methods used to precipitate the samples are related to the conformational preferences in the solid state. β1 ? β2 interconversion is possible by reprecipitation of the sample. Preferential stabilization of the β1- or β2-forms is strongly dependent on the residue number. Films of the oligomers, made by casting them from a dimethylformamide solution onto NaCl or KBr plates, take up an α-helical structure, and the α → β1 or α → β2 transition depends on the residue number of the cast film. | |||||
フォーマット | ||||||
内容記述タイプ | Other | |||||
内容記述 | application/pdf |