Abstract
In-cell distance determination by electron paramagnetic resonance (EPR) spectroscopy reveals essential structural information about biomacromolecules under native conditions. We demonstrate that the pulsed EPR technique RIDME (relaxation induced dipolar modulation enhancement) can be utilized for such distance determination. The performance of in-cell RIDME has been assessed at Q-band using stiff molecular rulers labeled with Gd(III)-PyMTA and microinjected into Xenopus laevis oocytes. The overtone coefficients are determined to be the same for protonated aqueous solutions and inside cells. As compared to in-cell DEER (double electron-electron resonance, also abbreviated as PELDOR), in-cell RIDME features approximately 5 times larger modulation depth and does not show artificial broadening in the distance distributions due to the effect of pseudosecular terms.
| Original language | English |
|---|---|
| Pages (from-to) | 1477-1481 |
| Number of pages | 5 |
| Journal | Journal of Physical Chemistry Letters |
| Volume | 10 |
| Issue number | 7 |
| DOIs | |
| Publication status | Published - Apr 2019 |
| Externally published | Yes |
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