Literature DB >> 18491846

PELDOR measurements on a nitroxide-labeled Cu(II) porphyrin: orientation selection, spin-density distribution, and conformational flexibility.

Bela E Bode1, Jörn Plackmeyer, Thomas F Prisner, Olav Schiemann.   

Abstract

Metal ions are functionally or structurally important centers in metalloproteins or RNAs, which makes them interesting targets for spectroscopic investigations. In combination with site-directed spin labeling, pulsed electron-electron double resonance (PELDOR or DEER) could be a well-suited method to characterize and localize them. Here, we report on the synthesis, full characterization, and PELDOR study of a copper(II) porphyrin/nitroxide model system. The X-band PELDOR time traces contain besides the distance information a convolution of orientational selectivity, conformational flexibility, exchange coupling, and spin density distribution, which can be deconvoluted by experiments with different frequency offsets and simulations. The simulations are based on the known experimental and spin Hamiltonian parameters and make use of a geometric model as employed for structurally similar bis-nitroxides and spin density parameters as obtained from density functional theory calculations. It is found that orientation selection with respect to dipolar angles is only weakly resolvable at X-band frequencies due to the large nitrogen hyperfine coupling of the copper porphyrin. On the other hand, the PELDOR time traces reveal a much faster oscillation damping than observed for structurally similar bis-nitroxides, which is mainly assigned to a small distribution in exchange couplings J. Taking the effects of orientation selectivity, distribution in J, and spin density distribution into account leads finally to a narrow distance distribution caused solely by the flexibility of the structure, which is in agreement with distributions from known bis-nitroxides of similar structure. Thus, X-band PELDOR measurements at different frequency offsets in combination with explicit time trace simulations allow for distinguishing between structural models and quantitative interpretation of copper-nitroxide PELDOR data gives access to localization of copper(II) ions.

Entities:  

Mesh:

Substances:

Year:  2008        PMID: 18491846     DOI: 10.1021/jp710504k

Source DB:  PubMed          Journal:  J Phys Chem A        ISSN: 1089-5639            Impact factor:   2.781


  20 in total

1.  Copper uptake induces self-assembly of 18.5 kDa myelin basic protein (MBP).

Authors:  Timo Bund; Joan M Boggs; George Harauz; Nadja Hellmann; Dariush Hinderberger
Journal:  Biophys J       Date:  2010-11-03       Impact factor: 4.033

Review 2.  Spin labeling EPR.

Authors:  Johann P Klare; Heinz-Jürgen Steinhoff
Journal:  Photosynth Res       Date:  2009-08-29       Impact factor: 3.573

3.  The double-histidine Cu²⁺-binding motif: a highly rigid, site-specific spin probe for electron spin resonance distance measurements.

Authors:  Timothy F Cunningham; Miriam R Putterman; Astha Desai; W Seth Horne; Sunil Saxena
Journal:  Angew Chem Int Ed Engl       Date:  2015-03-27       Impact factor: 15.336

4.  Characterization of the solution structure of human serum albumin loaded with a metal porphyrin and fatty acids.

Authors:  Matthias J N Junk; Hans W Spiess; Dariush Hinderberger
Journal:  Biophys J       Date:  2011-05-04       Impact factor: 4.033

5.  Light-Induced Triplet-Triplet Electron Resonance Spectroscopy.

Authors:  Arnau Bertran; Kevin B Henbest; Marta De Zotti; Marina Gobbo; Christiane R Timmel; Marilena Di Valentin; Alice M Bowen
Journal:  J Phys Chem Lett       Date:  2020-12-11       Impact factor: 6.475

6.  ESR spectroscopy identifies inhibitory Cu2+ sites in a DNA-modifying enzyme to reveal determinants of catalytic specificity.

Authors:  Zhongyu Yang; Michael R Kurpiewski; Ming Ji; Jacque E Townsend; Preeti Mehta; Linda Jen-Jacobson; Sunil Saxena
Journal:  Proc Natl Acad Sci U S A       Date:  2012-04-09       Impact factor: 11.205

7.  Orthogonal spin labeling and Gd(III)-nitroxide distance measurements on bacteriophage T4-lysozyme.

Authors:  Luca Garbuio; Enrica Bordignon; Evan K Brooks; Wayne L Hubbell; Gunnar Jeschke; Maxim Yulikov
Journal:  J Phys Chem B       Date:  2013-03-08       Impact factor: 2.991

8.  EPR relaxation-enhancement-based distance measurements on orthogonally spin-labeled T4-lysozyme.

Authors:  Sahand Razzaghi; Evan K Brooks; Enrica Bordignon; Wayne L Hubbell; Maxim Yulikov; Gunnar Jeschke
Journal:  Chembiochem       Date:  2013-06-14       Impact factor: 3.164

9.  Interaction between Prion Protein's Copper-Bound Octarepeat Domain and a Charged C-Terminal Pocket Suggests a Mechanism for N-Terminal Regulation.

Authors:  Eric G B Evans; M Jake Pushie; Kate A Markham; Hsiau-Wei Lee; Glenn L Millhauser
Journal:  Structure       Date:  2016-06-02       Impact factor: 5.006

10.  Sensitive Cu2+-Cu2+ distance measurements in a protein-DNA complex by double-quantum coherence ESR.

Authors:  Sharon Ruthstein; Ming Ji; Preeti Mehta; Linda Jen-Jacobson; Sunil Saxena
Journal:  J Phys Chem B       Date:  2013-05-10       Impact factor: 2.991

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.