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Investigation of the Stabilizing Mechanism of Collagen

Investigation of the Stabilizing Mechanism of Collagen
胶原蛋白稳定机制的研究
批准号:
16390016
负责人:
KOBAYASHI Yuji
金额:
$6.08万
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (B)
财政年份:
2004
资助国家:
日本
项目状态:
已结题
起止时间:
2004 至 2005

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中文摘要
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英文摘要
It has been known that Hyp^R residue contributes to the thermal stability of the collagen triple helical structure. We have performed intensive studies to investigate the stabilizing mechanism of the collagen triple helical structure using a series of polytripeptides (X-Y-Gly)_n [X, Y : Pro, Hyp^R, or 4-fluoroproline (fPro)] from the thermodynamic point of view. The thermodynamic parameters with the transition from the triple-helix to the single-coil determined by DSC analyses indicated that the enhanced stabilities are classified into two different types : the enthalpy term is primarily responsible for increased stability of (Pro-Hyp^R-Gly)_<10>, whereas the entropy term dominates the enhanced stabilities of (Pro-fPro^R-Gly)_<10> and (fPro^s-Pro-Gly)_<10>. We showed that this difference comes from the difference of hydration on these peptides by the comparison of molecular volumes observed in solution with intrinsic ones from the crystal structure.On the other hand, it has been shown … More that Hyp^R residue at the X position decreases the stability of the triple helix. To address this effect of Hyp^R, we have synthesized and characterized (Hyp^R-Hyp^R-Gly)_<10>. We have already reported that it takes a thermally stable triple helix, however, its stabilizing mechanism has not been solved. Here we determined the full-length crystal structure of (Hyp^R-Hyp^R-Gly)_<10>. To corroborate this precise structural information, we estimated the degrees of hydration in both the triple-helix and the single-coil states. The results showed that the degree of hydration of (Hyp^R-Hyp^R-Gly)_<10> is comparable to that of (Pro-Hyp^R-Gly)_<10> in the triple-helix state, but the former was more highly hydrated than (Pro-Hyp^R-Gly)_<10> in the single-coil state. Because hydration reduces the enthalpy due to the formation of hydrogen bond with water molecule and diminishes the entropy due to the restriction of water molecules surrounding a peptide molecule, we deduced that the high thermal stability of (Hyp^R-Hyp^R-Gly)_<10> is attributed to its high degree of hydration in the single-coil state. Less
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DOI: 10.1016/j.jmb.2004.10.011
发表时间: 2004-12-10
期刊: JOURNAL OF MOLECULAR BIOLOGY
影响因子: 5.6
作者: [Nishimura, M, Yoshida, T, Kobayashi, Y]
通讯作者: Kobayashi, Y
Conformational analysis of human calcitonin in solution
溶液中人降钙素的构象分析
DOI: --
发表时间: 2006
期刊: J. Pept. Sci. 12
影响因子: --
作者: [宮田 興子, 白井 淳, 吉野 新太郎, 中林 俊樹, 武田 良文, 内藤 猛章, Kiyoshi Ogawa et al.]
通讯作者: Kiyoshi Ogawa et al.
High-resolution X-ray structure of the unexpectedly stable dimer of the [Lys(-2)-Arg(-1)-des(17-21)]endothelin-1 peptide.
[Lys(-2)-Arg(-1)-des(17-21)]endothelin-1 肽出乎意料稳定的二聚体的高分辨率 X 射线结构。
DOI: 10.1021/bi049098a
发表时间: 2004
期刊: Biochemistry
影响因子: 2.9
作者: [F. Hoh, R. Cerdan, Q. Kaas, Y. Nishi, L. Chiche, S. Kubo, N. Chino, Yuji Kobayashi, C. Dumas, A. Aumelas]
通讯作者: A. Aumelas
Different Effects of 4-Hydroxyproline and 4-Fluoroproine on the Stability of Collagen Triple Helix
4-羟脯氨酸和4-氟脯氨酸对胶原三螺旋稳定性的不同影响
DOI: --
发表时间: 2005
期刊: Biochemistry (in press)
影响因子: --
作者: [Nishi, Y. et al.]
通讯作者: Y. et al.
26
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    • 批准号:
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    • 项目类别:
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    • 资助金额:
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    • 财政年份:
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    • 项目类别:
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    • 批准号:
      21390013
    • 项目类别:
      Grant-in-Aid for Scientific Research (B)
    • 资助金额:
      $12.31万
    • 财政年份:
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    • 负责人:
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    • 项目类别:
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    • 财政年份:
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