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假蓝铜蛋白的定点突变体:基于X射线结构及氧化还原电位差计算对氧化还原电位升高的解释

Site-directed mutants of pseudoazurin: explanation of increased redox potentials from X-ray structures and from calculation of redox potential differences.

作者信息

Libeu C A, Kukimoto M, Nishiyama M, Horinouchi S, Adman E T

机构信息

Department of Biological Structure, University of Washington, Box 357420, Seattle, Washington 98195-7420, USA.

出版信息

Biochemistry. 1997 Oct 28;36(43):13160-79. doi: 10.1021/bi9704111.

Abstract

In order to understand the origins of differences in redox potentials among cupredoxins (small blue type I copper-containing proteins that reversibly change oxidation state and interact with redox partners), we have determined the structures of the native and two mutants (P80A and P80I) of pseudoazurin from Alcaligenes faecalis S-6 in oxidized and reduced forms at resolutions of 2.2 A in the worst case and 1.6 A in the best case. The P80A mutation creates a surface pocket filled by a new water molecule, whereas the P80I mutant excludes this water. Distinct patterns of change occur in response to reduction for all three molecules: the copper position shifts, Met 7 and Pro 35 move, and the relative orientations of residues 81 to 16, 18 to the amide planes of 77 and 86, all change. Systematic changes in the weak electrostatic interactions seen in the structures of different oxidation states can explain the Met 7/Pro 35 structural differences as well as some fluctuating solvent positions. Overall displacement parameters increase reversibly upon reduction. The reduced forms are slightly expanded over the oxidized forms. The geometries of the mutants become more trigonal in their reduced forms, consistent with higher redox potentials (+409 mV for P80A and +450 mV for P80I). Calculations of the differences in redox potentials, using POLARIS, reveal that a water unique to the P80A mutant is required (with correctly oriented hydrogens) to approximate the observed difference in redox potential. The POLARIS calculations suggest that the reduced forms are additionally stabilized through changes in the solvation of the copper center, specifically via the amides of residues 16, 39, 41, 79, and 80 which interact with either Phe 18, Met 86, or Cys 78. The redox potential of P80A is increased largely due to solvation effects, whereas the redox potential of P80I is increased largely due to geometrical effects.

摘要

为了理解铜蓝蛋白(一类可逆改变氧化态并与氧化还原伙伴相互作用的小型蓝色I型含铜蛋白质)之间氧化还原电位差异的起源,我们测定了粪产碱菌S-6假单胞蓝蛋白的天然形式以及两个突变体(P80A和P80I)在氧化态和还原态下的结构,最差分辨率为2.2 Å,最佳分辨率为1.6 Å。P80A突变产生了一个被新水分子填充的表面口袋,而P80I突变体则排除了这个水分子。对于所有三个分子,还原时都会出现不同的变化模式:铜的位置发生移动,甲硫氨酸7和脯氨酸35移动,并且残基81至16、18至77和86酰胺平面的相对取向都发生变化。在不同氧化态结构中观察到的弱静电相互作用的系统变化可以解释甲硫氨酸7/脯氨酸35的结构差异以及一些波动的溶剂位置。还原时整体位移参数可逆增加。还原形式比氧化形式略有扩展。突变体的几何形状在还原形式下变得更加三角化,这与更高的氧化还原电位一致(P80A为+409 mV,P80I为+450 mV)。使用POLARIS计算氧化还原电位的差异表明,需要P80A突变体特有的一个水分子(氢原子取向正确)来近似观察到的氧化还原电位差异。POLARIS计算表明,还原形式通过铜中心溶剂化的变化而进一步稳定,具体是通过与苯丙氨酸18、甲硫氨酸86或半胱氨酸78相互作用的残基16、39、41、79和80的酰胺。P80A的氧化还原电位大幅增加主要是由于溶剂化效应,而P80I的氧化还原电位大幅增加主要是由于几何效应。

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