{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,10]],"date-time":"2026-06-10T16:45:31Z","timestamp":1781109931286,"version":"3.54.1"},"reference-count":51,"publisher":"National Academy of Sciences","issue":"8","content-domain":{"domain":["www.pnas.org"],"crossmark-restriction":true},"short-container-title":["Proc. Natl. Acad. Sci. U.S.A."],"published-print":{"date-parts":[[2002,4,16]]},"abstract":"<jats:p>\n                    Ferritin concentrates iron as a hydrous ferric oxide in a protein cavity (8 nm in diameter) by using eight pores along the threefold symmetry axes of the octahedral supramolecular structure. The role of ligand exchange in the entry of Fe(II) hexahydrate into ferritin protein has been studied with [Cr(TREN)(H\n                    <jats:sub>2<\/jats:sub>\n                    O)(OH)]\n                    <jats:sup>2+<\/jats:sup>\n                    [TREN = N(CH\n                    <jats:sub>2<\/jats:sub>\n                    CH\n                    <jats:sub>2<\/jats:sub>\n                    NH\n                    <jats:sub>2<\/jats:sub>\n                    )\n                    <jats:sub>3<\/jats:sub>\n                    ], a model for Fe(H\n                    <jats:sub>2<\/jats:sub>\n                    O)\n                    <jats:sub>6<\/jats:sub>\n                    <jats:sup>2+<\/jats:sup>\n                    with only two exchangeable ligands. The results show that five different ferritin proteins, varying in pore structure, oxidation sites, and nucleation sites, bind Cr(TREN) at functional protein sites, based on inhibition of iron mineralization and oxidation. Properties of Cr(TREN)\u2013ferritin adducts include an increased isoelectric point, a shift in the Cr(TREN) UV\/vis spectrum consistent with exchange of water for protein carboxylate or thiolate ligands, binding affinities of 50\u2013250 \u03bcM, and a slow rate of dissociation (\n                    <jats:italic>k<\/jats:italic>\n                    = 4 \u00d7 10\n                    <jats:sup>\u22126<\/jats:sup>\n                    sec\n                    <jats:sup>\u22121<\/jats:sup>\n                    ). The relationship of Cr(TREN) inhibition of iron oxidation and mineralization by Cr(TREN) to the known structures of the various ferritins tested suggests that Cr(TREN) plugs the ferritin pores, obstructing Fe(II) entry in folded and unfolded pores. Because only two exchangeable waters are sufficient for pore binding of Cr(TREN), the physiological Fe(II) donor must bind to the pore with few exchangeable ligands. These results show the advantage of using stable model complexes to explore properties of transient Fe\u2013protein complexes during Fe mineralization in ferritin.\n                  <\/jats:p>","DOI":"10.1073\/pnas.032089399","type":"journal-article","created":{"date-parts":[[2002,7,26]],"date-time":"2002-07-26T10:45:09Z","timestamp":1027680309000},"page":"5195-5200","update-policy":"https:\/\/doi.org\/10.1073\/pnas.cm10313","source":"Crossref","is-referenced-by-count":33,"title":["Iron uptake in ferritin is blocked by binding of [Cr(TREN)(H\n                    <sub>2<\/sub>\n                    O)(OH)]\n                    <sup>2+<\/sup>\n                    , a slow dissociating model for [Fe(H\n                    <sub>2<\/sub>\n                    O)\n                    <sub>6<\/sub>\n                    ]\n                    <sup>2+<\/sup>"],"prefix":"10.1073","volume":"99","author":[{"given":"Carmen 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