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马脾铁蛋白中铁核的形成:磁化率、pH值及成分研究。

Iron core formation in horse spleen ferritin: magnetic susceptibility, pH, and compositional studies.

作者信息

Hilty S, Webb B, Frankel R B, Watt G D

机构信息

Department of Chemistry, Brigham Young University, Provo, Utah 84602.

出版信息

J Inorg Biochem. 1994 Nov 15;56(3):173-85. doi: 10.1016/0162-0134(94)85004-6.

Abstract

Horse spleen ferritin (HoSF) reconstituted with small iron cores ranging in size from 8 to 500 iron atoms was studied by magnetic susceptibility and pH measurements to determine when the added Fe3+ begins to aggregate and form antiferromagnetically coupled clusters and also to determine the hydrolytic state of the iron at low iron loading. The Evans NMR magnetic susceptibility measurements showed that at iron loadings as low as 8 Fe3+/HoSF, at least half of the added iron atoms were involved in antiferromagnetic exchange interactions and the other half were present as isolated iron atoms with S = 5/2. As the core size increased to about 24 iron atoms, the antiferromagnetic exchange interactions among the iron atoms increased until reaching the limiting value of 3.8 Bohr magnetons per iron atom, the value present in holo HoSF. HoSF containing eight or more Fe3+ to which eight Fe2+ were added showed that the Fe2+ ions were at sites remote from the Fe3+ and that the resulting HoSF consisted of individual, noninteracting Fe2+ and the partially aggregated Fe3+. pH measurements for core reduction showed that Fe(OH)3 was initially present at all iron loadings but that in the absence of iron chelators the reduced iron core is partially hydrolyzed. Proton induced x-ray emission spectroscopy showed that Cl- is transported into the iron core during reduction, forming a stable chlorohydroxy Fe(II) mineral phase.

摘要

通过磁化率和pH测量研究了用大小在8到500个铁原子之间的小铁芯重构的马脾铁蛋白(HoSF),以确定添加的Fe3+何时开始聚集并形成反铁磁耦合簇,同时确定低铁负载量时铁的水解状态。埃文斯核磁共振磁化率测量表明,在低至8个Fe3+/HoSF的铁负载量下,至少一半添加的铁原子参与了反铁磁交换相互作用,另一半以S = 5/2的孤立铁原子形式存在。随着核心尺寸增加到约24个铁原子,铁原子之间的反铁磁交换相互作用增强,直至达到每个铁原子3.8玻尔磁子的极限值,即全铁HoSF中的值。向含有八个或更多Fe3+的HoSF中添加八个Fe2+,结果表明Fe2+离子位于远离Fe3+的位点,所得的HoSF由单个、不相互作用的Fe2+和部分聚集的Fe3+组成。核心还原的pH测量表明,在所有铁负载量下最初都存在Fe(OH)3,但在没有铁螯合剂的情况下,还原的铁芯会部分水解。质子诱导X射线发射光谱表明,在还原过程中Cl-被转运到铁芯中,形成稳定的氯羟基Fe(II)矿物相。

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