Literature DB >> 18947176

The Mn(2+)-bicarbonate complex in a frozen solution revisited by pulse W-band ENDOR.

Alexey Potapov1, Daniella Goldfarb.   

Abstract

The coordination of bicarbonate to Mn (2+) is the simplest model system for the coordination of Mn (2+) to carboxylate residues in a protein. Recently, the structure of such a complex has been investigated by means of X-band pulse EPR (electron paramagnetic resonance) experiments ( Dasgupta, J. ; et al. J. Phys. Chem. B 2006, 110, 5099 ). Based on the EPR results, together with electrochemical titrations, it has been concluded that the Mn (2+) bicarbonate complex consists of two bicarbonate ligands, one of which is monodentate and other bidentate, but only the latter has been observed by the pulsed EPR techniques. The X-band measurements, however, suffer several drawbacks. (i) The zero-field splitting (ZFS) term of the spin Hamiltonian affects the nuclear frequencies. (ii) There are significant contributions from ENDOR (electron nuclear double resonance) lines of the M S not equal +/- (1)/ 2 manifolds. (iii) There are overlapping signals of (23)Na. All these reduce the uniqueness of the data interpretation. Here we present a high-field ENDOR investigation of Mn (2+)/NaH (13)CO 3 in a water/methanol solution that eliminates the above difficulties. Both Davies and Mims ENDOR measurements were carried out. The spectra show that a couple of slightly inequivalent (13)C nuclei are present, with isotropic and anisotropic hyperfine couplings of A iso1 = 1.2 MHz, T perpendicular1 = 0.7 MHz, A iso2 = 1.0 MHz, T perpendicular2 = 0.6 MHz, respectively. The sign of the hyperfine coupling was determined by variable mixing time (VMT) ENDOR measurements. These rather close hyperfine parameters suggest that there are either two distinct, slightly different, carbonate ligands or that there is some distribution in conformation in only one ligand. The distances extracted from T perpendicular1 and T perpendicular2 are consistent with a monodentate binding mode. The monodentate binding mode and the presence of two ligands were further supported by DFT calculations and (1)H ENDOR measurements. Additionally, (23)Na ENDOR resolved at least two types of (23)Na (+) in the Mn (2+)-bicarbonate complex, thus suggesting that the bicarbonate bridges two positively charged metal ions.

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Year:  2008        PMID: 18947176     DOI: 10.1021/ic8011316

Source DB:  PubMed          Journal:  Inorg Chem        ISSN: 0020-1669            Impact factor:   5.165


  5 in total

1.  Combining steady-state and dynamic methods for determining absolute signs of hyperfine interactions: pulsed ENDOR Saturation and Recovery (PESTRE).

Authors:  Peter E Doan
Journal:  J Magn Reson       Date:  2010-10-14       Impact factor: 2.229

2.  13C ENDOR reveals that the D1 polypeptide C-terminus is directly bound to Mn in the photosystem II oxygen evolving complex.

Authors:  Jamie A Stull; Troy A Stich; Rachel J Service; Richard J Debus; Sanjay K Mandal; William H Armstrong; R David Britt
Journal:  J Am Chem Soc       Date:  2010-01-20       Impact factor: 15.419

3.  Detection of Water Molecules on the Radical Transfer Pathway of Ribonucleotide Reductase by 17O Electron-Nuclear Double Resonance Spectroscopy.

Authors:  Fabian Hecker; JoAnne Stubbe; Marina Bennati
Journal:  J Am Chem Soc       Date:  2021-05-06       Impact factor: 15.419

Review 4.  Manganese acquisition and homeostasis at the host-pathogen interface.

Authors:  John P Lisher; David P Giedroc
Journal:  Front Cell Infect Microbiol       Date:  2013-12-05       Impact factor: 5.293

5.  13C ENDOR Spectroscopy of Lipoxygenase-Substrate Complexes Reveals the Structural Basis for C-H Activation by Tunneling.

Authors:  Masaki Horitani; Adam R Offenbacher; Cody A Marcus Carr; Tao Yu; Veronika Hoeke; George E Cutsail; Sharon Hammes-Schiffer; Judith P Klinman; Brian M Hoffman
Journal:  J Am Chem Soc       Date:  2017-01-25       Impact factor: 15.419

  5 in total

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