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The Fate Of Iron Released From Heme By Hemeoxygenase-1, Jonathan Mark Gardner
The Fate Of Iron Released From Heme By Hemeoxygenase-1, Jonathan Mark Gardner
Undergraduate Honors Capstone Projects
A strain of Escherichia coli was genetically modified to co-express human heme oxygenase-1 and ferritin. The E. coli were then grown with varying amounts of hemin to see if the iron released upon degradation of the hemin by heme oxygenase-1 is loaded into ferritin. Following incubation, the ferritin was purified and the amount of iron loaded into ferritin determined. It was found that ferritin purifed from E. coli expressing human heme oxygenase-1 contained more iron than E. coli that did not contain human heme oxygenase-1. It was concluded that some of the iron released upon degradation of hemin by heme …
Oxidative Damage Caused By Iron Loading Into Ferritin, Talina Christensen Watts
Oxidative Damage Caused By Iron Loading Into Ferritin, Talina Christensen Watts
Undergraduate Honors Capstone Projects
Ferritin is the iron storage protein found in humans, animals, plants, fungi and bacteria. We are interested in how iron is loaded and stored in mammalian ferritin. Ferrous iron must be oxidized to ferric iron in order to be stored in ferritin. It is generally believed that ferritin does the loading itself, dependant upon a "ferroxidase activity." Oxidation of iron can result in the production of the hydroxyl radical which can cause oxidative damage to surrounding proteins and other biomolecules. An indicator of oxidative damage to proteins is the formation of carbonyl groups. Using only the H subunit of human …