Literature DB >> 24036469

Moving difference (MDIFF) non-adiabatic rapid sweep (NARS) EPR of copper(II).

James S Hyde1, Brian Bennett, Aaron W Kittell, Jason M Kowalski, Jason W Sidabras.   

Abstract

Non-adiabatic rapid sweep (NARS) EPR spectroscopy has been introduced for application to nitroxide-labeled biological samples (Kittell et al., 2011). Displays are pure absorption, and are built up by acquiring data in spectral segments that are concatenated. In this paper we extend the method to frozen solutions of copper-imidazole, a square planar copper complex with four in-plane nitrogen ligands. Pure absorption spectra are created from concatenation of 170 5-gauss segments spanning 850 G at 1.9 GHz. These spectra, however, are not directly useful since nitrogen superhyperfine couplings are barely visible. Application of the moving difference (MDIFF) algorithm to the digitized NARS pure absorption spectrum is used to produce spectra that are analogous to the first harmonic EPR. The signal intensity is about four times higher than when using conventional 100 kHz field modulation, depending on line shape. MDIFF not only filters the spectrum, but also the noise, resulting in further improvement of the SNR for the same signal acquisition time. The MDIFF amplitude can be optimized retrospectively, different spectral regions can be examined at different amplitudes, and an amplitude can be used that is substantially greater than the upper limit of the field modulation amplitude of a conventional EPR spectrometer, which improves the signal-to-noise ratio of broad lines.
Copyright © 2013 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Biological copper; Direct detection; EPR; ESR; MDIFF; Moving average; NARS; Non-adiabatic rapid sweep

Mesh:

Substances:

Year:  2013        PMID: 24036469      PMCID: PMC3919454          DOI: 10.1016/j.jmr.2013.08.004

Source DB:  PubMed          Journal:  J Magn Reson        ISSN: 1090-7807            Impact factor:   2.229


  14 in total

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2.  Molecular motion in spin-labeled phospholipids and membranes.

Authors:  W L Hubbell; H M McConnell
Journal:  J Am Chem Soc       Date:  1971-01-27       Impact factor: 15.419

3.  The octarepeat domain of the prion protein binds Cu(II) with three distinct coordination modes at pH 7.4.

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Authors:  Aaron W Kittell; Theodore G Camenisch; Joseph J Ratke; Jason W Sidabras; James S Hyde
Journal:  J Magn Reson       Date:  2011-06-13       Impact factor: 2.229

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Authors:  J S Hyde; W Froncisz
Journal:  Annu Rev Biophys Bioeng       Date:  1982

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Authors:  Aaron W Kittell; Eric J Hustedt; James S Hyde
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7.  Labile conformation of type 2 Cu2+ centres in human ceruloplasmin.

Authors:  V V Rylkov; K A Moshkov
Journal:  Eur J Biochem       Date:  1991-04-10

8.  EPR of Cu2+ prion protein constructs at 2 GHz using the g(perpendicular) region to characterize nitrogen ligation.

Authors:  James S Hyde; Brian Bennett; Eric D Walter; Glenn L Millhauser; Jason W Sidabras; William E Antholine
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  10 in total

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Authors:  Brian Bennett; Jason M Kowalski
Journal:  Methods Enzymol       Date:  2015-07-23       Impact factor: 1.600

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7.  Rapid-scan EPR of immobilized nitroxides.

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