Binding of Cu(II) or Zn(II) in a de novo designed triple-stranded α-helical coiled-coil toward a prototype for a metalloenzyme

被引:41
作者
Kiyokawa, T
Kanaori, K
Tajima, K
Koike, M
Mizuno, T
Oku, JI
Tanaka, T [2 ]
机构
[1] Kyoto Inst Technol, Dept Appl Biol, Sakyo Ku, Kyoto 6068585, Japan
[2] Nagoya Inst Technol, Dept Mat Sci, Grad Sch Engn, Nagoya, Aichi 4668555, Japan
来源
JOURNAL OF PEPTIDE RESEARCH | 2004年 / 63卷 / 04期
关键词
coiled-coil; de novo design; folding; helical structures; metalloproteins;
D O I
10.1111/j.1399-3011.2004.00109.x
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We previously reported the IZ-3adH peptide, which formed a triple-stranded coiled-coil after binding Ni(II), Cu(II), or Zn(II). In this paper, we report the peptide, IZ-3aH, having a new metal binding specificity. The IZ-3aH peptide was found to bind Cu(II) and Zn(II) and form a triple-stranded coiled-coil. However, it did not bind Ni(II). Metal ion titrations monitored by circular dichroism revealed that the dissociation constants, K-d were 9 muM for Zn(II) and 10 muM for Cu(II). The bound Cu(II) ion has a planar tetragonal geometry, where the coordination positions are three nitrogens of the His residues and one H2O.
引用
收藏
页码:347 / 353
页数:7
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