| Item type |
デフォルトアイテムタイプ_（フル）(1) |
| 公開日 |
2023-03-18 |
| タイトル |
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|
タイトル |
Participation of the surface structure of pharaonis phoborhodopsin, ppR and its A149S and A149V mutants, consisting of the C-terminal α-helix and E-F loop, in the complex-formation with the cognate transducer pHtrII, as revealed by site-directed 13C solid-state NMR |
|
言語 |
en |
| 作成者 |
Kawamura, Izuru
Ikeda, Yoichi
Sudo, Yuki
Iwamoto, Masayuki
Shimono, Kazumi
Yamaguchi, Satoru
Tuzi, Satoru
Saito, Hazime
Kamo, Naoki
Naito, Akira
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| アクセス権 |
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アクセス権 |
open access |
|
アクセス権URI |
http://purl.org/coar/access_right/c_abf2 |
| 権利情報 |
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|
権利情報 |
Author Posting. (c) The Authors (2007) This is the author's version of the work. It is posted here for personal use, not for redistribution. The definitive version was published in PHOTOCHEMISTRY AND PHOTOBIOLOGY, 83(2): 339-345. http://dx.doi.org/10.1562/2006-06-20-RA-940 |
| 主題 |
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主題Scheme |
NDC |
|
主題 |
460 |
| 内容記述 |
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内容記述 |
We have recorded 13C solid state NMR spectra of [3-13C]Ala-labeled pharaonis phoborhodopsin ppR, and its mutants, A149S and A149V, complexed with the cognate transducer pHtrII (1-159), to gain insight into a possible role of their cytoplasmic surface structure including the C-terminal α-helix and E-F loop for stabilization of the 2:2 complex, by both cross-polarization magic angle spinning (CP-MAS) and dipolar decoupled-magic angle spinning (DD-MAS) NMR techniques. We found that 13C CP-MAS NMR spectra of [3-13C]Ala-ppR, A149S, and A149V complexed with the transducer pHtrII are very similar, reflecting their conformation and dynamics changes caused by mutual interactions through the transmembrane α-helical surfaces. In contrast, their DD-MAS NMR spectral features are quite different between [3-13C]Ala- A149S and A149V in the complexes with pHtrII: 13C DD-MAS NMR spectrum of [3-13C]Ala-A149S complex is rather similar to that of the uncomplexed form, while the corresponding spectral feature of A149V complex is similar to that of ppR complex in the C-terminal tip region. This is because more flexible surface structure detected by the DD-MAS NMR spectra are more directly influenced by the dynamics changes than the CP-MAS NMR. It turned out, therefore, that an altered surface structure of A149S resulted in destabilized complex as viewed from the 13C NMR spectrum of the surface areas, probably because of modified conformation at the corner of the helix F in addition to the change of hydropathy. It is, therefore, concluded that the surface structure of ppR including the C-terminal α-helix and the E-F loops is directly involved in the stabilization of the complex through conformational stability of the helix F. |
|
言語 |
en |
| 出版者 |
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出版者 |
American Society of Photobiology |
| 言語 |
|
|
言語 |
eng |
| 資源タイプ |
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資源タイプ識別子 |
http://purl.org/coar/resource_type/c_6501 |
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資源タイプ |
journal article |
| 出版タイプ |
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出版タイプ |
AO |
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出版タイプResource |
http://purl.org/coar/version/c_b1a7d7d4d402bcce |
| 関連情報 |
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|
識別子タイプ |
DOI |
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|
関連識別子 |
10.1562/2006-06-20-RA-940 |
| 関連情報 |
|
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|
識別子タイプ |
DOI |
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|
関連識別子 |
http://dx.doi.org/10.1562/2006-06-20-RA-940 |
| 収録物識別子 |
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収録物識別子タイプ |
ISSN |
|
収録物識別子 |
0031-8655 |
| 収録物識別子 |
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|
収録物識別子タイプ |
NCID |
|
収録物識別子 |
AA00773103 |
| 開始ページ |
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|
開始ページ |
339 |
| 書誌情報 |
Photochemistry and Photobiology
Photochemistry and Photobiology
巻 83,
号 2,
p. 339-345,
発行日 2007-03
|
| 旧ID |
20662 |
PhotochemPhotobiol_83-2_339.pdf (424.3 KB)
