A High-Affinity Metal-Binding Peptide from Escherichia coli HypB

被引:31
作者
Chung, Kim C. Chan [1 ]
Cao, Li [1 ]
Dias, Alistair V. [1 ]
Pickering, Ingrid J. [2 ]
George, Graham N. [2 ]
Zamble, Deborah B. [1 ]
机构
[1] Univ Toronto, Dept Chem, Toronto, ON M5S 3H6, Canada
[2] Univ Saskatchewan, Dept Geol Sci, Saskatoon, SK S7N 5E2, Canada
基金
加拿大健康研究院; 加拿大自然科学与工程研究理事会;
关键词
D O I
10.1021/ja8055003
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The high-affinity nickel-binding site of the Escherichia coli [NiFe]-hydrogenase accessory protein HypB was localized to residues at the immediate N-terminus of the protein. Modification of a metal-binding fusion protein, site-directed mutagenesis experiments, and DFT calculations were used to identify the N-terminal amine as a ligand as well as the three cysteine residues in the CXXCGCXXX motif. This sequence can be removed from the protein and both a synthesized peptide and a protein fusion bind nickel with a similar affinity and the same structure as the parent metalloprotein, indicating the self-sufficiency of this high-affinity nickel-binding sequence.
引用
收藏
页码:14056 / +
页数:3
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