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  1. AU="Horiguchi, Kumiko"
  2. AU="Wagner, Franz F"
  3. AU="Mishra, Vandana"
  4. AU=Zucker Irving H
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  6. AU="Andrea Benedetti"
  7. AU="Xu, Jiyu"
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  10. AU="Maunik Chapala"
  11. AU="Luksic, Ivica"
  12. AU="Mastronardi, Luciano"
  13. AU="Md Farijul Islam"
  14. AU="Quansah, Gabriel W"
  15. AU="Keane, Stephen"
  16. AU="Marsela, Enklajd"
  17. AU="Tate, Amanda W"
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  1. Artikel ; Online: Parallel β-Sheet Structure of Alanine Tetrapeptide in the Solid State As Studied by Solid-State NMR Spectroscopy.

    Asakura, Tetsuo / Horiguchi, Kumiko / Aoki, Akihiro / Tasei, Yugo / Naito, Akira

    The journal of physical chemistry. B

    2016  Band 120, Heft 34, Seite(n) 8932–8941

    Abstract: The structural analysis of alanine oligopeptides is important for understanding the crystalline region in silks from spiders and wild silkworms and also the mechanism of cellular toxicity of human diseases arising from expansion in polyalanine sequences. ...

    Abstract The structural analysis of alanine oligopeptides is important for understanding the crystalline region in silks from spiders and wild silkworms and also the mechanism of cellular toxicity of human diseases arising from expansion in polyalanine sequences. The atomic-level structures of alanine tripeptide and tetrapeptide with antiparallel β-sheet structures (AP-Ala3 and AP-Ala4, respectively) together with alanine tripeptide with parallel β-sheet structures (P-Ala3) have been determined, but alanine tetrapeptide with a parallel β-sheet structure (P-Ala4) has not been reported yet. In this article, first, we established the preparation protocol of P-Ala4 from more stable AP-Ala4. Second, complete assignments of the (13)C, (15)N, and (1)H solid-state NMR spectra were performed with (13)C- and (15)N-labeled Ala4 samples using several solid-state NMR techniques. Then, the structural constraints were obtained, for example, the amide proton peaks of P-Ala4 in the (1)H double-quantum magic-angle spinning NMR spectrum were heavily overlapped and observed at about 7.4 ppm, which was a much higher field than that of 8.7-9.1 ppm observed for AP-Ala4, indicating that the intermolecular hydrogen-bond lengths across strands (N-H···O═C) were considerably longer for P-Ala4, that is, 2.21-2.34 Å, than those reported for AP-Ala4, that is, 1.8-1.9 Å. The structural model was proposed for P-Ala4 by NMR results and MD calculations.
    Sprache Englisch
    Erscheinungsdatum 2016-09-01
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ISSN 1520-5207
    ISSN (online) 1520-5207
    DOI 10.1021/acs.jpcb.6b06292
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel: Parallel β-Sheet Structure of Alanine Tetrapeptide in the Solid State As Studied by Solid-State NMR Spectroscopy

    Asakura, Tetsuo / Horiguchi Kumiko / Aoki Akihiro / Tasei Yugo / Naito Akira

    Journal of physical chemistry. 2016 Sept. 01, v. 120, no. 34

    2016  

    Abstract: The structural analysis of alanine oligopeptides is important for understanding the crystalline region in silks from spiders and wild silkworms and also the mechanism of cellular toxicity of human diseases arising from expansion in polyalanine sequences. ...

    Abstract The structural analysis of alanine oligopeptides is important for understanding the crystalline region in silks from spiders and wild silkworms and also the mechanism of cellular toxicity of human diseases arising from expansion in polyalanine sequences. The atomic-level structures of alanine tripeptide and tetrapeptide with antiparallel β-sheet structures (AP-Ala₃ and AP-Ala₄, respectively) together with alanine tripeptide with parallel β-sheet structures (P-Ala₃) have been determined, but alanine tetrapeptide with a parallel β-sheet structure (P-Ala₄) has not been reported yet. In this article, first, we established the preparation protocol of P-Ala₄ from more stable AP-Ala₄. Second, complete assignments of the ¹³C, ¹⁵N, and ¹H solid-state NMR spectra were performed with ¹³C- and ¹⁵N-labeled Ala₄ samples using several solid-state NMR techniques. Then, the structural constraints were obtained, for example, the amide proton peaks of P-Ala₄ in the ¹H double-quantum magic-angle spinning NMR spectrum were heavily overlapped and observed at about 7.4 ppm, which was a much higher field than that of 8.7–9.1 ppm observed for AP-Ala₄, indicating that the intermolecular hydrogen-bond lengths across strands (N–H···OC) were considerably longer for P-Ala₄, that is, 2.21–2.34 Å, than those reported for AP-Ala₄, that is, 1.8–1.9 Å. The structural model was proposed for P-Ala₄ by NMR results and MD calculations.
    Schlagwörter Araneae ; alanine ; cytotoxicity ; human diseases ; hydrogen bonding ; models ; nitrogen ; nuclear magnetic resonance spectroscopy ; oligopeptides ; silk ; stable isotopes
    Sprache Englisch
    Erscheinungsverlauf 2016-0901
    Umfang p. 8932-8941.
    Erscheinungsort American Chemical Society
    Dokumenttyp Artikel
    ISSN 1520-5207
    DOI 10.1021%2Facs.jpcb.6b06292
    Datenquelle NAL Katalog (AGRICOLA)

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  3. Artikel ; Online: Difference in the structures of alanine tri- and tetra-peptides with antiparallel β-sheet assessed by X-ray diffraction, solid-state NMR and chemical shift calculations by GIPAW.

    Asakura, Tetsuo / Yazawa, Koji / Horiguchi, Kumiko / Suzuki, Furitsu / Nishiyama, Yusuke / Nishimura, Katsuyuki / Kaji, Hironori

    Biopolymers

    2014  Band 101, Heft 1, Seite(n) 13–20

    Abstract: Alanine oligomers provide a key structure for silk fibers from spider and wild silkworms.We report on structural analysis of L-alanyl-L-alanyl-L-alanyl-L-alanine (Ala)4 with anti-parallel (AP) β-structures using X-ray and solid-state NMR. All of the Ala ... ...

    Abstract Alanine oligomers provide a key structure for silk fibers from spider and wild silkworms.We report on structural analysis of L-alanyl-L-alanyl-L-alanyl-L-alanine (Ala)4 with anti-parallel (AP) β-structures using X-ray and solid-state NMR. All of the Ala residues in the (Ala)4 are in equivalent positions, whereas for alanine trimer (Ala)3 there are two alternative locations in a unit cell as reported previously (Fawcett and Camerman, Acta Cryst., 1975, 31, 658-665). (Ala)4 with AP β-structure is more stable than AP-(Ala)3 due to formation of the stronger hydrogen bonds. The intermolecular structure of (Ala)4 is also different from polyalanine fiber structure, indicating that the interchain arrangement of AP β-structure changes with increasing alanine sequencelength. Furthermore the precise (1)H positions, which are usually inaccesible by X-ray diffraction method, are determined by high resolution (1)H solid state NMR combined with the chemical shift calculations by the gauge-including projector augmented wave method.
    Mesh-Begriff(e) Alanine/chemistry ; Animals ; Characidae ; Magnetic Resonance Spectroscopy ; Peptides/chemistry ; Silk/chemistry ; X-Ray Diffraction
    Chemische Substanzen Peptides ; Silk ; Alanine (OF5P57N2ZX)
    Sprache Englisch
    Erscheinungsdatum 2014-01
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1123-x
    ISSN 1097-0282 ; 0006-3525
    ISSN (online) 1097-0282
    ISSN 0006-3525
    DOI 10.1002/bip.22241
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  4. Artikel ; Online: Two different packing arrangements of antiparallel polyalanine.

    Asakura, Tetsuo / Okonogi, Michi / Horiguchi, Kumiko / Aoki, Akihiro / Saitô, Hazime / Knight, David P / Williamson, Mike P

    Angewandte Chemie (International ed. in English)

    2012  Band 51, Heft 5, Seite(n) 1212–1215

    Mesh-Begriff(e) Alanine/chemistry ; Crystallization ; Crystallography, X-Ray ; Humans ; Models, Molecular ; Peptides/chemistry
    Chemische Substanzen Peptides ; polyalanine (25191-17-7) ; Alanine (OF5P57N2ZX)
    Sprache Englisch
    Erscheinungsdatum 2012-01-27
    Erscheinungsland Germany
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2011836-3
    ISSN 1521-3773 ; 1433-7851
    ISSN (online) 1521-3773
    ISSN 1433-7851
    DOI 10.1002/anie.201105356
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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