Crystal structure of the CueO mutants at Glu506, the key amino acid located in the proton transfer pathway for dioxygen reduction

被引:9
作者
Komori, Hirofumi [1 ]
Kajikawa, Takao [2 ]
Kataoka, Kunishige [2 ]
Higuchi, Yoshiki [3 ]
Sakurai, Takeshi [2 ]
机构
[1] Kagawa Univ, Fac Educ, Takamatsu, Kagawa 7608522, Japan
[2] Kanazawa Univ, Grad Sch Nat Sci & Technol, Kanazawa, Ishikawa 9201192, Japan
[3] Univ Hyogo, Grad Sch Life Sci, Kamigori, Ako 6781297, Japan
关键词
CueO; Multicopper oxidase; Proton transfer; O-2-reduction; Hydrogen bond network; X-ray crystal structure; Site-directed mutagenesis; COPPER EFFLUX OXIDASE; MULTICOPPER OXIDASE; 4-ELECTRON REDUCTION; BILIRUBIN-OXIDASE; I COPPER; MUTATIONS; INTERMEDIATE; CLEAVAGE; ADJACENT; ROLES;
D O I
10.1016/j.bbrc.2013.07.121
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Glu506 involved in the hydrogen bond network leading from solvent waters to the trinuclear copper center in a multicopper oxidase, CueO plays a crucial role to transport protons in the four-electron reduction of dioxygen to water. We performed X-ray crystal structure analyses of the Glu506Ala and Glu506Ile mutants, showing the formation of a compensatory proton transport pathway with only water molecules and a disruption of the hydrogen bond network due to the bulky side chain, respectively. We discuss the efficiency of proton transport through the hydrogen bond network based on the present results and our previous modification of the proton transport pathway by the Glu506 to Gln mutation, which have allowed us to trap and characterize the reaction intermediates. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:686 / 690
页数:5
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