Younkyoo Kim, Gerald T. Babcock, Kristene K. Surerus, James A. Fee, R. Brian Dyer, William H. Woodruff, W. Anthony Oertling
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Abstract
The cyanide isotope-sensitive low-frequency vibrations of ferrous cyano complexes of cytochrome a 3 are studied for cytochrome ba 3 from Thermus thermophilus and cytochrome aa 3 from bovine heart. Cyanide complexes of ba 3 display three isotope sensitive frequencies at 512, 485, and 473 cm−1 . The first is primarily an Fe—C stretching motion, whereas the lower wavenumber modes are bending motions. These iron-cyanide vibrations are independent of the redox levels of the other metal centers in the protein. On the other hand, the fully reduced bovine derivative complexed with cyanide gives rise to a bending vibration at 503 cm−1 and a stretching vibration at 469 cm−1 . That is, the ordering of the stretching and bending frequencies is reversed from that of the bacterial protein. These results are analyzed by normal coordinate calculations to obtain comparative models for the binuclear O2 reducing site of the two proteins. We find that the observed frequencies are consistent with a linear Fe—C—N group and larger Fe—C stretching force constant (2.558 mdyn/Å) for ba 3 and a slightly bent Fe—C—N group (angle ∼ 170°) and a smaller Fe—C stretching force constant (2.335 mdyn/Å) for aa 3 . Thus, there are significant differences in the interaction of cyanide with ferrous a 3 in the two proteins that are most likely caused by a weaker proximal histidine interaction and stronger peripheral heme electron withdrawing effects in ba 3 . Possible sources of these protein-induced effects are discussed. Using the analysis developed here, comparison of the FeCN stretching and bending frequencies of the ferrous bovine a 3 -CN complex to those obtained from the ferric a 3 -CN complex suggests that upon conversion of the resting to the fully reduced protein, a conformational change occurs that constrains the ligand binding site. © 1998 John Wiley & Sons, Inc. Biospectroscopy 4: 1–15, 1998
血红素-铜氧化酶中的氰化物结合和活性位点结构:细胞色素ba3和aa3的CN -配合物的铁氰化物振动的正坐标分析
研究了嗜热热菌细胞色素ba3和牛心脏细胞色素aa3的氰化物同位素敏感低频振动。ba3的氰化物配合物在512、485和473 cm−1处显示出三个同位素敏感频率。第一种主要是Fe-C拉伸运动,而低波数模式是弯曲运动。这些铁氰化物的振动与蛋白质中其他金属中心的氧化还原水平无关。另一方面,与氰化物完全还原的牛衍生物在503 cm−1处产生弯曲振动,在469 cm−1处产生拉伸振动。也就是说,拉伸和弯曲频率的顺序与细菌蛋白质的顺序相反。这些结果通过正坐标计算进行分析,得到两种蛋白双核O2还原位点的比较模型。我们发现观测到的频率与ba3的线性Fe-C - n群和较大的Fe-C拉伸力常数(2.558 mdyn/Å)一致,而aa3的Fe-C - n群(角度约170°)和较小的Fe-C拉伸力常数(2.335 mdyn/Å)一致。因此,两种蛋白中氰化物与亚铁a3的相互作用存在显著差异,这很可能是由于ba3中近端组氨酸的相互作用较弱,而外周血红素的电子抽离作用较强。讨论了这些蛋白质诱导效应的可能来源。利用本文开发的分析,比较了牛亚铁a3-CN络合物与铁a3-CN络合物的FeCN拉伸和弯曲频率,表明在将静止蛋白转化为完全还原蛋白时,发生了限制配体结合位点的构象变化。©1998 John Wiley &儿子,Inc。生物光谱学学报,1998,19 (4):1104 - 1104
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