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钙通道拮抗剂ω-芋螺毒素的圆二色光谱

Circular dichroism spectra of calcium channel antagonist omega-conotoxins.

作者信息

Kim J I, Ohtake A, Sato K

机构信息

Mitsubishi Kasei Institute of Life Sciences, Machida-shi, Tokyo, Japan.

出版信息

Biochem Biophys Res Commun. 1997 Jan 3;230(1):133-5. doi: 10.1006/bbrc.1996.5900.

DOI:10.1006/bbrc.1996.5900
PMID:9020029
Abstract

The circular dichroism (CD) spectrum of omega-conotoxin GVIA is quite different from those of omega-conotoxin MVIIA and MVIIC, despite their distinct similarity in three dimensional structures. In order to characterize the unique CD spectrum of omega-conotoxin GVIA, we focused our attention on the aromatic chromophore and analyzed the CD spectra of three synthetic analogs, in which Tyr13, Tyr22, and Tyr27 were individually replaced by alanine. Replacement of Tyr27 caused a significant change in both the near- and far-ultraviolet CD spectrum of omega-conotoxin GVIA and resulted in the omega-conotoxin MVIIA/MVIIC-like pattern, suggesting that Tyr27 has a dominant contribution to the unique CD profile of omega-conotoxin GVIA.

摘要

尽管ω-芋螺毒素GVIA、MVIIA和MVIIC在三维结构上有明显的相似性,但它们的圆二色性(CD)光谱却大不相同。为了表征ω-芋螺毒素GVIA独特的CD光谱,我们将注意力集中在芳香发色团上,并分析了三种合成类似物的CD光谱,其中酪氨酸13、酪氨酸22和酪氨酸27分别被丙氨酸取代。酪氨酸27的取代导致ω-芋螺毒素GVIA的近紫外和远紫外CD光谱都发生了显著变化,并产生了类似ω-芋螺毒素MVIIA/MVIIC的模式,这表明酪氨酸27对ω-芋螺毒素GVIA独特的CD谱有主要贡献。

相似文献

1
Circular dichroism spectra of calcium channel antagonist omega-conotoxins.钙通道拮抗剂ω-芋螺毒素的圆二色光谱
Biochem Biophys Res Commun. 1997 Jan 3;230(1):133-5. doi: 10.1006/bbrc.1996.5900.
2
Tyr13 is essential for the activity of omega-conotoxin MVIIA and GVIA, specific N-type calcium channel blockers.酪氨酸13对于ω-芋螺毒素MVIIA和GVIA(特异性N型钙通道阻滞剂)的活性至关重要。
Biochem Biophys Res Commun. 1995 Jan 17;206(2):449-54. doi: 10.1006/bbrc.1995.1063.
3
Tyr13 is essential for the binding of omega-conotoxin MVIIC to the P/Q-type calcium channel.酪氨酸13对于ω-芋螺毒素MVIIC与P/Q型钙通道的结合至关重要。
Biochem Biophys Res Commun. 1995 Sep 14;214(2):305-9. doi: 10.1006/bbrc.1995.2288.
4
Structure-activity relationships of omega-conotoxins MVIIA, MVIIC and 14 loop splice hybrids at N and P/Q-type calcium channels.ω-芋螺毒素MVIIA、MVIIC及14个环剪接杂合体在N型和P/Q型钙通道上的构效关系
J Mol Biol. 1999 Jun 25;289(5):1405-21. doi: 10.1006/jmbi.1999.2817.
5
Folding of omega-conotoxins. 1. Efficient disulfide-coupled folding of mature sequences in vitro.ω-芋螺毒素的折叠。1. 成熟序列在体外的高效二硫键偶联折叠。
Biochemistry. 1996 Dec 3;35(48):15537-46. doi: 10.1021/bi961574c.
6
Role of basic residues for the binding of omega-conotoxin GVIA to N-type calcium channels.碱性残基在ω-芋螺毒素GVIA与N型钙通道结合中的作用。
Biochem Biophys Res Commun. 1993 Aug 16;194(3):1292-6. doi: 10.1006/bbrc.1993.1964.
7
Three-dimensional structure in solution of the calcium channel blocker omega-conotoxin MVIIA.钙通道阻滞剂ω-芋螺毒素MVIIA在溶液中的三维结构。
Biochemistry. 1995 Aug 15;34(32):10256-65. doi: 10.1021/bi00032a020.
8
Binding of chimeric analogs of omega-conotoxin MVIIA and MVIIC to the N- and P/Q-type calcium channels.ω-芋螺毒素MVIIA和MVIIC嵌合类似物与N型和P/Q型钙通道的结合
FEBS Lett. 1997 Sep 8;414(2):480-4. doi: 10.1016/s0014-5793(97)01056-9.
9
Solution structure of omega-conotoxin MVIIC, a high affinity ligand of P-type calcium channels, using 1H NMR spectroscopy and complete relaxation matrix analysis.利用核磁共振氢谱和完全弛豫矩阵分析法解析ω-芋螺毒素MVIIC(P型钙通道的高亲和力配体)的溶液结构
J Mol Biol. 1995 Apr 21;248(1):106-24. doi: 10.1006/jmbi.1995.0205.
10
Synthesis, bioactivity, and cloning of the L-type calcium channel blocker omega-conotoxin TxVII.
Biochemistry. 1999 Sep 28;38(39):12876-84. doi: 10.1021/bi990731f.

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