The effect of spin polarization on double electron–electron resonance (DEER) spectroscopy
-
Published:2022-07-01
Issue:1
Volume:3
Page:101-110
-
ISSN:2699-0016
-
Container-title:Magnetic Resonance
-
language:en
-
Short-container-title:Magn. Reson.
Author:
Sweger Sarah R.ORCID, Denysenkov Vasyl P., Maibaum Lutz, Prisner Thomas F.ORCID, Stoll StefanORCID
Abstract
Abstract. Double electron–electron resonance (DEER) spectroscopy measures the distribution of distances between two electron spins in the nanometer range, often on doubly spin-labeled proteins, via the modulation of a refocused spin echo by the dipolar interaction between the spins. DEER is commonly conducted under conditions where the polarization of the spins is small. Here, we examine the DEER signal under conditions of high spin polarization, thermally obtainable at low temperatures and high magnetic fields, and show that the signal acquires a polarization-dependent out-of-phase component both for the intramolecular and intermolecular contributions. For the latter, this corresponds to a phase shift of the spin echo that is linear in the pump pulse position. We derive a compact analytical form of this phase shift and show experimental measurements using monoradical and biradical nitroxides at several fields and temperatures. The effect highlights a novel aspect of the fundamental spin physics underlying DEER spectroscopy.
Funder
National Institutes of Health
Publisher
Copernicus GmbH
Reference42 articles.
1. Abdullin, D., Brehm, P., Fleck, N., Spicher, S., Grimme, S., and Schiemann, O.:
Pulsed EPR dipolar spectroscopy on spin pairs with one highly anisotropic
spin center: the low-spin FeIII case, Eur. J. Chem., 25, 14388–14398,
https://doi.org/10.1002/chem.201902908, 2019. a 2. Barth, K., Hank, S., Spindler, P. E., Prisner, T. F., Tampé, R., and
Joseph, B.: Conformational coupling and trans-inhibition in the human antigen
transporter ortholog TmrAB resolved with dipolar EPR spectroscopy,
J. Am. Chem. Soc., 140, 4527–4533,
https://doi.org/10.1016/0009-2614(94)87059-4, 2018. a 3. Bode, B. E., Margraf, D., Plackmeyer, J., Dürner, G., Prisner, T. F., and
Schiemann, O.: Counting the monomers in nanometer-sized oligomers by pulsed
electron–electron double resonance, J. Am. Chem. Soc., 129, 6736–6745,
https://doi.org/10.1021/ja065787t, 2007. a 4. Born, A., Soetbeer, J., Breitgoff, F., Henen, M. A., Sgourakis, N., Polyhach,
Y., Nichols, P. J., Strotz, D., Jeschke, G., and Vögeli, B.:
Reconstruction of coupled intra-and interdomain protein motion from nuclear
and electron magnetic resonance, J. Am. Chem. Soc., 143, 16055–16067,
https://doi.org/10.1021/jacs.1c06289, 2021. a 5. Bowen, A. M., Jones, M. W., Lovett, J. E., Gaule, T. G., McPherson, M. J.,
Dilworth, J. R., Timmel, C. R., and Harmer, J. R.: Exploiting
orientation-selective DEER: determining molecular structure in systems
containing Cu (II) centres, Phys. Chem. Chem. Phys., 18, 5981–5994, https://doi.org/10.1039/C5CP06096F, 2016. a
Cited by
5 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
|
|