{"id":628,"date":"2026-04-15T13:27:03","date_gmt":"2026-04-15T13:27:03","guid":{"rendered":"https:\/\/citations.tools.bio-logic.fr\/?p=628"},"modified":"2026-04-15T13:27:03","modified_gmt":"2026-04-15T13:27:03","slug":"addition-of-oxygen-to-the-diironii-ii-cluster-is-the-slowest-step-in-formation-of-the-tyrosyl-radical-in-the-w103y-variant-of-ribonucleotide-reductase-protein-r2-from-mouse","status":"publish","type":"post","link":"https:\/\/citations.tools.bio-logic.fr\/?p=628","title":{"rendered":"Addition of Oxygen to the Diiron(II\/II) Cluster Is the Slowest Step in Formation of the Tyrosyl Radical in the W103Y Variant of Ribonucleotide Reductase Protein R2 from Mouse"},"content":{"rendered":"<h4>DOI:<\/h4>\n<p><a href=\"https:\/\/doi.org\/10.1021\/bi7003747\" target=\"_blank\" rel=\"noopener\">10.1021\/bi7003747<\/a><\/p>\n<h4>Authors:<\/h4>\n<p>Danny Yun, Lana Saleh, Ricardo Garc\u00eda\u2010Serres, Brandon M. Chicalese, Young Hun An, Boi Hanh Huynh, J. Martin Bollinger<\/p>\n<h4>Abstract:<\/h4>\n<p>Activation of O2 by the diiron(II\/II) cluster in protein R2 of class I ribonucleotide reductase generates the enzyme&rsquo;s essential tyrosyl radical. A crucial step in this reaction is the transfer of an electron from solution to a diiron(II\/II)-O2 adduct during formation of the radical-generating, diiron(III\/IV) intermediate X. In the reaction of R2 from Escherichia coli, this electron injection is initiated by the rapid (&gt;400 s-1 at 5 degrees C), transient oxidation of the near-surface residue, tryptophan 48, to a cation radical and is blocked by substitution of W48 with F, A, G, Y, L, or Q. By contrast, a study of the cognate reaction in protein R2 from mouse suggested that electron injection might be the slowest step in generation of its tyrosyl radical, Y177* [Schmidt, P. P., Rova, U., Katterle, B., Thelander, L., and Gr\u00e4slund, A. (1998) J. Biol. Chem. 273, 21463-21472]. The crucial evidence was the observation that Y177* production is slowed by approximately 30-fold upon substitution of W103, the cognate of the electron-shuttling W48 in E. coli R2, with tyrosine. In this work, we have applied stopped-flow absorption and freeze-quench electron paramagnetic resonance and M\u00f6ssbauer spectroscopies to the mouse R2 reaction to evaluate the possibility that an already sluggish electron-transfer step is slowed by 30-fold by substitution of this key residue. The drastically reduced accumulation of cluster X, failure of precursors to the intermediate to accumulate, and, most importantly, first-order dependence of the rate of Y177* formation on the concentration of O2 prove that addition of O2 to the diiron(II\/II) cluster, rather than electron injection, is the slowest step in the R2-W103Y reaction. This finding indicates that the basis for the slowing of Y177* formation by the W103Y substitution is an unexpected secondary effect on the structure or dynamics of the protein, its diiron(II\/II) cluster, or both rather than the expected chemical effect on the electron injection step.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>DOI: 10.1021\/bi7003747 Authors: Danny Yun, Lana Saleh, Ricardo Garc\u00eda\u2010Serres, Brandon M. Chicalese, Young Hun An, Boi Hanh Huynh, J. Martin Bollinger Abstract: Activation of O2 by the diiron(II\/II) cluster in protein R2 of class I ribonucleotide reductase generates the enzyme&rsquo;s essential tyrosyl radical. A crucial step in this reaction is the transfer of an electron [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[5],"tags":[],"class_list":["post-628","post","type-post","status-publish","format-standard","hentry","category-freeze-quench"],"_links":{"self":[{"href":"https:\/\/citations.tools.bio-logic.fr\/index.php?rest_route=\/wp\/v2\/posts\/628","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/citations.tools.bio-logic.fr\/index.php?rest_route=\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/citations.tools.bio-logic.fr\/index.php?rest_route=\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/citations.tools.bio-logic.fr\/index.php?rest_route=\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/citations.tools.bio-logic.fr\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=628"}],"version-history":[{"count":0,"href":"https:\/\/citations.tools.bio-logic.fr\/index.php?rest_route=\/wp\/v2\/posts\/628\/revisions"}],"wp:attachment":[{"href":"https:\/\/citations.tools.bio-logic.fr\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=628"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/citations.tools.bio-logic.fr\/index.php?rest_route=%2Fwp%2Fv2%2Fcategories&post=628"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/citations.tools.bio-logic.fr\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=628"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}