Literature DB >> 18351402

Structural basis for VO2+ inhibition of nitrogenase activity (A): 31P and 23Na interactions with the metal at the nucleotide binding site of the nitrogenase Fe protein identified by ENDOR spectroscopy.

Jan Petersen1, Karl Fisher, David J Lowe.   

Abstract

We previously reported the vanadyl hyperfine couplings of VO(2+)-ATP and VO(2+)-ADP complexes in the presence of the nitrogenase Fe protein from Klebsiella pneumoniae (Petersen et al. in Biochemistry 41:13253-13263, 2002). It was demonstrated that different VO(2+)-nucleotide coordination environments coexist and are distinguishable by electron paramagnetic resonance (EPR) spectroscopy. Here orientation-selective continuous-wave electron-nuclear double resonance (ENDOR) spectra have been investigated especially in the low-radio-frequency range in order to identify superhyperfine interactions with nuclei other than protons. Some of these resonances have been attributed to the presence of a strong interaction with a 31P nucleus although no resolvable superhyperfine structure due to 31P or other nuclei was detected in the EPR spectra. The superhyperfine coupling component is determined to be about 25 MHz. Such a 31P coupling is consistent with an interaction of the metal with phosphorus from a directly, equatorially coordinated nucleotide phosphate group(s). Additionally, novel more prominent 31P ENDOR signals are detected in the low-frequency region. Some of these correspond to a relatively weak 31P coupling. This coupling is present with ATP for all pH forms but is absent with ADP. The ENDOR resonances of these weakly coupled 31P are likely to originate from an interaction of the metal with a nucleotide phosphate group of the nucleoside triphosphate and are attributed to a phosphorus with axial characteristics. Another set of resonances, split about the nuclear Zeeman frequency of 23Na, was detected, suggesting that a monovalent Na+ ion is closely associated with the divalent metal-nucleotide binding site. Na+ replacement by K+ unambiguously confirmed that ENDORs at radio frequencies between 3.0 and 4.5 MHz arise from an interaction with Na+ ions. In contrast to the low-frequency 31P signal, these resonances are present in spectra with both ADP and ATP, and for both low- and neutral-pH forms, although slight differences are detected, showing that these are sensitive to the nucleotide and pH.

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Year:  2008        PMID: 18351402     DOI: 10.1007/s00775-008-0360-0

Source DB:  PubMed          Journal:  J Biol Inorg Chem        ISSN: 0949-8257            Impact factor:   3.358


  53 in total

1.  A Q-band pulse EPR/ENDOR spectrometer and the implementation of advanced one- and two-dimensional pulse EPR methodology.

Authors:  I Gromov; J Shane; J Forrer; R Rakhmatoullin; Y Rozentzwaig; A Schweiger
Journal:  J Magn Reson       Date:  2001-04       Impact factor: 2.229

2.  Mn2+-adenosine nucleotide complexes in the presence of the nitrogenase iron-protein: detection of conformational rearrangements directly at the nucleotide binding site by EPR and 2D-ESEEM (two-dimensional electron spin-echo envelope modulation spectroscopy).

Authors:  Jan Petersen; Christof Gessner; Karl Fisher; Claire J Mitchell; David J Lowe; Wolfgang Lubitz
Journal:  Biochem J       Date:  2005-11-01       Impact factor: 3.857

3.  Effect of magnesium adenosine 5'-triphosphate on the accessibility of the iron of clostridial azoferredoxin, a component of nitrogenase.

Authors:  G A Walker; L E Mortenson
Journal:  Biochemistry       Date:  1974-05-21       Impact factor: 3.162

4.  Structure of ADP x AIF4(-)-stabilized nitrogenase complex and its implications for signal transduction.

Authors:  H Schindelin; C Kisker; J L Schlessman; J B Howard; D C Rees
Journal:  Nature       Date:  1997-05-22       Impact factor: 49.962

5.  Structural analysis of metal ion ligation to nucleotides and nucleic acids using pulsed EPR spectroscopy.

Authors:  Charles G Hoogstraten; Christopher V Grant; Thomas E Horton; Victoria J DeRose; R David Britt
Journal:  J Am Chem Soc       Date:  2002-02-06       Impact factor: 15.419

6.  The role of the Mg2+ cation in ATPsynthase studied by electron paramagnetic resonance using VO2+ and Mn2+ paramagnetic probes.

Authors:  J L Zimmermann; B Schneider; S Morlet; T Amano; C Sigalat
Journal:  Spectrochim Acta A Mol Biomol Spectrosc       Date:  2000-02-01       Impact factor: 4.098

7.  Visible, EPR and electron nuclear double-resonance spectroscopic studies on the two metal-binding sites of oxovanadium (IV)-substituted D-xylose isomerase.

Authors:  R Bogumil; J Hüttermann; R Kappl; R Stabler; C Sudfeldt; H Witzel
Journal:  Eur J Biochem       Date:  1991-03-14

8.  Circular dichroism and magnetic circular dichroism of nitrogenase proteins.

Authors:  P J Stephens; C E McKenna; B E Smith; H T Nguyen; M C McKenna; A J Thomson; F Devlin; J B Jones
Journal:  Proc Natl Acad Sci U S A       Date:  1979-06       Impact factor: 11.205

Review 9.  Vanadium in cancer treatment.

Authors:  Angelos M Evangelou
Journal:  Crit Rev Oncol Hematol       Date:  2002-06       Impact factor: 6.312

10.  Effects of nucleotides on the protein ligands to metals at the M2 and M3 metal-binding sites of the spinach chloroplast F1-ATPase.

Authors:  A L Houseman; R LoBrutto; W D Frasch
Journal:  Biochemistry       Date:  1995-03-14       Impact factor: 3.162

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  1 in total

1.  Structural basis for VO(2+)-inhibition of nitrogenase activity: (B) pH-sensitive inner-sphere rearrangements in the 1H-environment of the metal coordination site of the nitrogenase Fe-protein identified by ENDOR spectroscopy.

Authors:  Jan Petersen; Claire J Mitchell; Karl Fisher; David J Lowe
Journal:  J Biol Inorg Chem       Date:  2008-05       Impact factor: 3.358

  1 in total

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