Photoactive peptides for light-initiated tyrosyl radical generation and transport into ribonucleotide reductase

Steven Y. Reece, Mohammad R. Seyedsayamdost, Jo Anne Stubbe, Daniel G. Nocera

Research output: Contribution to journalArticle

35 Scopus citations

Abstract

The mechanism of radical transport in the α2 (R1) subunit of class I E. coli ribonucleotide reductase (RNR) has been investigated by the phototriggered generation of a tyrosyl radical, Y356, on a 20-mer peptide bound to α2. This peptide, Y-R2C19, is identical to the C-terminal peptide tail of the β2 (R2) subunit and is a known competitive inhibitor of binding of the native β2 protein to α2. Y356 radical initiation is prompted by excitation (λ ≥ 300 nm) of a proximal anthraquinone, Anq, or benzophenone, BPA, chromophore on the peptide. Transient absorption spectroscopy has been employed to kinetically characterize the radical-producing step by time resolving the semiquinone anion (Anq•-), ketyl radical (BPA), and Y photoproducts on (i) BPA-Y and Anq-Y dipeptides and (ii) BPA/Anq-Y-R2C19 peptides. Light-initiated, single-turnover assays have been carried out with the peptide/α2 complex in the presence of [ 14C]-labeled cytidine 5′-diphosphate substrate and ATP allosteric effector. We show that both the Anq-and BPA-containing peptides are competent in deoxycytidine diphosphate formation and turnover occurs via Y731 to Y730 to C439 pathway-dependent radical transport in α2. Experiments with the Y730F mutant exclude a direct superexchange mechanism between C439 and Y731 and are consistent with a PCET model for radical transport in which there is a unidirectional transport of the electron and proton transport among residues of α2.

Original languageEnglish (US)
Pages (from-to)8500-8509
Number of pages10
JournalJournal of the American Chemical Society
Volume129
Issue number27
DOIs
StatePublished - Jul 11 2007

All Science Journal Classification (ASJC) codes

  • Catalysis
  • Chemistry(all)
  • Biochemistry
  • Colloid and Surface Chemistry

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