George E Cutsail1, Elizabeth J Blaesi2, Christopher J Pollock2, J Martin Bollinger3, Carsten Krebs3, Serena DeBeer4. 1. Max Planck Institute for Chemical Energy Conversion, Stiftstrasse 34-36, D-45470 Mülheim an der Ruhr, Germany. 2. Department of Chemistry, The Pennsylvania State University, University Park, PA 16802, United States. 3. Department of Chemistry, The Pennsylvania State University, University Park, PA 16802, United States; Department of Biochemistry and Molecular Biology, The Pennsylvania State University, University Park, PA 16802, United States. 4. Max Planck Institute for Chemical Energy Conversion, Stiftstrasse 34-36, D-45470 Mülheim an der Ruhr, Germany. Electronic address: Serena.DeBeer@cec.mpg.de.
Abstract
Ferritin-like carboxylate-bridged non-heme diiron enzymes activate O2 for a variety of difficult reactions throughout nature. These reactions often begin by abstraction of hydrogen from strong CH bonds. The enzymes activate O2 at their diferrous cofactors to form canonical diferric peroxo intermediates, with a range of possible coordination modes. Herein, we explore the ability of high-energy resolution fluorescence detected X-ray absorption spectroscopy (HERFD XAS) to provide insight into the nature of peroxo level intermediates in non-heme diiron proteins. Freeze quenched (FQ) peroxo intermediates from p-aminobenzoate N-oxygenase (AurF), aldehyde-deformylating oxygenase (ADO), and the β subunit of class Ia ribonucleotide reductase from Escherichia coli (Ecβ) are investigated. All three intermediates are proposed to adopt different peroxo binding modes, and each exhibit different Fe Kα HERFD XAS pre-edge features and intensities. As these FQ-trapped samples consist of multiple species, deconvolution of HERFD XAS spectra based on speciation, as determined by Mössbauer spectroscopy, is also necessitated - yielding 'pure' diferric peroxo HERFD XAS spectra from dilute protein samples. Finally, the impact of a given peroxo coordination mode on the HERFD XAS pre-edge energy and intensity is evaluated through time-dependent density functional theory (TDDFT) calculations of the XAS spectra on a series of hypothetical model complexes, which span a full range of possible peroxo coordination modes to a diferric core. The utility of HERFD XAS for future studies of enzymatic intermediates is discussed.
Ferritin-like n class="Chemical">carboxylate-bridged non-heme diiron enzymes activate O2 for a variety of difficult reactions throughout nature. These reactions often begin by abstraction of hydrogen from strong CH bonds. The enzymes activate O2 at their diferrous cofactors to form canonical diferric peroxo intermediates, with a range of possible coordination modes. Herein, we explore the ability of high-energy resolution fluorescence detected X-ray absorption spectroscopy (HERFD XAS) to provide insight into the nature of peroxo level intermediates in non-heme diiron proteins. Freeze quenched (FQ) peroxo intermediates from p-aminobenzoateN-oxygenase (AurF), aldehyde-deformylating oxygenase (ADO), and the β subunit of class Ia ribonucleotide reductase from Escherichia coli (Ecβ) are investigated. All three intermediates are proposed to adopt different peroxo binding modes, and each exhibit different Fe Kα HERFD XAS pre-edge features and intensities. As these FQ-trapped samples consist of multiple species, deconvolution of HERFD XAS spectra based on speciation, as determined by Mössbauer spectroscopy, is also necessitated - yielding 'pure' diferric peroxo HERFD XAS spectra from dilute protein samples. Finally, the impact of a given peroxo coordination mode on the HERFD XAS pre-edge energy and intensity is evaluated through time-dependent density functional theory (TDDFT) calculations of the XAS spectra on a series of hypothetical model complexes, which span a full range of possible peroxo coordination modes to a diferric core. The utility of HERFD XAS for future studies of enzymatic intermediates is discussed.
Authors: E I Solomon; T C Brunold; M I Davis; J N Kemsley; S K Lee; N Lehnert; F Neese; A J Skulan; Y S Yang; J Zhou Journal: Chem Rev Date: 2000-01-12 Impact factor: 60.622
Authors: Andrew L. Feig; Michael Becker; Siegfried Schindler; Rudi van Eldik; Stephen J. Lippard Journal: Inorg Chem Date: 1996-04-24 Impact factor: 5.165
Authors: Andrew J Skulan; Thomas C Brunold; Jeffrey Baldwin; Lana Saleh; J Martin Bollinger; Edward I Solomon Journal: J Am Chem Soc Date: 2004-07-21 Impact factor: 15.419
Authors: Maria E Pandelia; Ning Li; Hanne Nørgaard; Douglas M Warui; Lauren J Rajakovich; Wei-Chen Chang; Squire J Booker; Carsten Krebs; J Martin Bollinger Journal: J Am Chem Soc Date: 2013-10-09 Impact factor: 15.419
Authors: Victoria Korneeva Korboukh; Ning Li; Eric W Barr; J Martin Bollinger; Carsten Krebs Journal: J Am Chem Soc Date: 2009-09-30 Impact factor: 15.419
Authors: Thomas Kroll; Michael L Baker; Samuel A Wilson; Marcus Lundberg; Amélie Juhin; Marie-Anne Arrio; James J Yan; Leland B Gee; Augustin Braun; Tsu-Chien Weng; Dimosthenis Sokaras; Britt Hedman; Keith O Hodgson; Edward I Solomon Journal: J Am Chem Soc Date: 2021-03-17 Impact factor: 15.419
Authors: Hannah Rosenbach; Eva Walla; George E Cutsail; James A Birrell; Marina Pascual-Ortiz; Serena DeBeer; Ursula Fleig; Ingrid Span Journal: J Biol Inorg Chem Date: 2021-02-05 Impact factor: 3.358
Authors: Franklin D Fuller; Anton Loukianov; Tsukasa Takanashi; Daehyun You; Yiwen Li; Kiyoshi Ueda; Thomas Fransson; Makina Yabashi; Tetsuo Katayama; Tsu-Chien Weng; Roberto Alonso-Mori; Uwe Bergmann; Jan Kern; Vittal K Yachandra; Philippe Wernet; Junko Yano Journal: Commun Chem Date: 2021-06-07
Authors: Chieh-Chih George Yeh; Thirakorn Mokkawes; Justin M Bradley; Nick E Le Brun; Sam P de Visser Journal: Chembiochem Date: 2022-05-23 Impact factor: 3.461
Authors: Sayanti Chatterjee; Ingolf Harden; Giovanni Bistoni; Rebeca G Castillo; Sonia Chabbra; Maurice van Gastel; Alexander Schnegg; Eckhard Bill; James A Birrell; Bill Morandi; Frank Neese; Serena DeBeer Journal: J Am Chem Soc Date: 2022-02-04 Impact factor: 15.419