Dudchenko N O, Mykhaĭlyk O M
Institute of Applied Problems in Physics and Biophysics of NAS of the Ukraine.
Ukr Biokhim Zh (1999). 1999 May-Jun;71(3):122-8.
The present paper deals with the procedure of a quantitative determination of chelatable iron in biological microsamples (20-50 mg) using an electron spin resonance technique based on the iron incorporation into the stable iron (III)-desferrioxamine B complexes. The conclusion is, that the method developed is valuable one to characterize the availability of iron from different sources. Using the method developed, the share of iron outside the protein core was shown to be less then 0.5 percentages of the whole iron content in the horse spleen ferritin suspension with 100 mg protein per ml and average iron content of 810 iron atoms per protein molecule. For a set of tissue samples taken from internal organs and brain of mice, rats and rabbits the data on chelatable iron concentration have been obtained.
本文论述了一种使用电子自旋共振技术对生物微量样品(20 - 50毫克)中可螯合铁进行定量测定的方法,该技术基于铁掺入稳定的铁(III)-去铁胺B络合物。结论是,所开发的方法对于表征不同来源铁的有效性是一种有价值的方法。使用所开发的方法,在每毫升含100毫克蛋白质且每个蛋白质分子平均含810个铁原子的马脾铁蛋白悬浮液中,蛋白质核心外的铁含量占总铁含量的比例不到0.5%。对于从小鼠、大鼠和兔子的内脏器官和大脑采集的一组组织样本,已获得了可螯合铁浓度的数据。