Literature DB >> 22386646

W-band PELDOR with 1 kW microwave power: molecular geometry, flexibility and exchange coupling.

Gunnar W Reginsson1, Robert I Hunter, Paul A S Cruickshank, David R Bolton, Snorri Th Sigurdsson, Graham M Smith, Olav Schiemann.   

Abstract

A technique that is increasingly being used to determine the structure and conformational flexibility of biomacromolecules is Pulsed Electron-Electron Double Resonance (PELDOR or DEER), an Electron Paramagnetic Resonance (EPR) based technique. At X-band frequencies (9.5 GHz), PELDOR is capable of precisely measuring distances in the range of 1.5-8 nm between paramagnetic centres but the orientation selectivity is weak. In contrast, working at higher frequencies increases the orientation selection but usually at the expense of decreased microwave power and PELDOR modulation depth. Here it is shown that a home-built high-power pulsed W-band EPR spectrometer (HiPER) with a large instantaneous bandwidth enables one to achieve PELDOR data with a high degree of orientation selectivity and large modulation depths. We demonstrate a measurement methodology that gives a set of PELDOR time traces that yield highly constrained data sets. Simulating the resulting time traces provides a deeper insight into the conformational flexibility and exchange coupling of three bisnitroxide model systems. These measurements provide strong evidence that W-band PELDOR may prove to be an accurate and quantitative tool in assessing the relative orientations of nitroxide spin labels and to correlate those orientations to the underlying biological structure and dynamics. Copyright Â
© 2012 Elsevier Inc. All rights reserved.

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Year:  2012        PMID: 22386646     DOI: 10.1016/j.jmr.2012.01.019

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


  12 in total

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5.  A New Wavelet Denoising Method for Experimental Time-Domain Signals: Pulsed Dipolar Electron Spin Resonance.

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8.  The use of the Rx spin label in orientation measurement on proteins, by EPR.

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10.  Protein-induced changes in DNA structure and dynamics observed with noncovalent site-directed spin labeling and PELDOR.

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Journal:  Nucleic Acids Res       Date:  2012-08-31       Impact factor: 16.971

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