电离辐射对血红蛋白的影响:血红蛋白的氧衍生物。

M N Bartlett, J M Stephenson, M C Symons
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引用次数: 4

摘要

已经确定的是,氧合血红蛋白暴露在电离辐射下会导致(FeO2)单元显著选择性地增加电子,产生一种新的电子(FeO2)-,其中额外的电子主要定位在铁和二氧上。这项工作现已扩展到血红蛋白(Hb)。岩手县。M. Iwate使用的血红蛋白是一种突变型血红蛋白,只有铁(III) α -链和氧-链(α 2 Met β 2氧)。α -链中的血红素铁原子在第5位由近端酪氨酸代替组氨酸协调。该单元为高自旋Fe(III),具有轴对称,在g = 6和g = 2区域具有显著的电子自旋共振(ESR)特征。在77 K下暴露于60Co伽马射线时,两种类型的铁中心都发生了有效的电子加成,产生了Fe(II)和(FeO2)-单位。前者通过Fe(III)的g = 6特征降低来监测,后者通过g-特征在2.254 (gx)、2.149 (gy)和1.967 (gz)处的增长来监测。这些值接近于正常氧合血红蛋白β链中形成的FeO2中心的值。在77 K以上退火时,发生了两个变化:首先是gx和gy的小幅但明显增加,其次是gx和gy的显著减少,使g值接近于直接在正常蛋白α链中形成的中心。最后,该中间种得到gx = 2.310, gy = 2.180, gz = 1.935的中心。这些值是典型的低自旋Fe(III)血红蛋白,并分配给质子化复合物Fe(III)O2H。最终,在大约室温下,它被转化为高自旋的,具有g = 6特征的相遇形式。这些结果证实了Hb的-链中心。Iwate的行为与孤立的-链相同。他们还证实,即使在每个四聚体中都有Fe(III)单元存在的情况下,电子向氧基的加成也很容易。结果还证实,电子捕获得到(FeO2)-单元后,并没有发生内部电子转移,从α链中的Fe(III)中心得到Fe(II)。
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Effect of ionizing radiation on haemoglobin: the oxy-derivative of haemoglobin Iwate.

It is well established that exposure of oxyhaemoglobin to ionizing radiation results in remarkably selective electron addition to the (FeO2) unit, giving a novel species, (FeO2)-, in which the extra electron is largely localized on iron and dioxygen. This work has now been extended to haemoglobin (Hb.) Iwate. The haemoglobin M. Iwate used is a mutant haemoglobin having only Fe(III) alpha-chains by oxy beta-chains (alpha 2 Met beta 2 oxy). The haem iron atoms in the alpha-chains are coordinated in the fifth site by a proximal tyrosine in place of histidine. This unit is a high-spin Fe(III) with axial symmetry and prominent electron spin resonance (ESR) features in the g = 6 and g = 2 regions. On exposure to 60Co gamma-rays at 77 K, efficient electron addition occurred at both types of iron centre, giving Fe(II) and (FeO2)- units. The former was monitored by the decrease of the g = 6 feature for Fe(III) and the latter by the growth of g-features at 2.254 (gx), 2.149 (gy) and 1.967 (gz). These values are close to those for the FeO2- centre formed in the beta-chains of normal oxyhaemoglobin. On annealing above 77 K, two changes occurred: first there was a small but clear increase in gx and gy, followed by a marked reduction in gx and gy giving g-values close to those for the centre formed directly in the alpha-chains of the normal protein. Finally, this intermediate species gave a centre having gx = 2.310, gy = 2.180 and gz = 1.935. These values are typical of low-spin Fe(III) haemoglobin and are assigned to the protonated complex, Fe(III)O2H. Ultimately at ca. room temperature, this was converted into the high-spin, met-form, with a gain in the g = 6 feature. These results established that the beta-chain centre in Hb. Iwate behave in the same way as isolated beta-chains. They also confirm that electron addition to the oxy-units is facile, even in the presence of Fe(III) units in each tetramer. The results also confirm that electron capture to give (FeO2)- units is not followed by internal electron-transfer to give Fe(II) from the Fe(III) centres in the alpha-chains.

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Proceedings of the Royal Society of London Series B-Containing Papers of Abiological Character
Proceedings of the Royal Society of London Series B-Containing Papers of Abiological Character 生命科学, 发育生物学与生殖生物学, 发育生物学
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