Abstract

The DEER (double electron-electron resonance, also called PELDOR) experiment, which probes the dipolar interaction between two spins and thus reveals distance information, is an important tool for structural studies. In recent years, shaped pump pulses have become a valuable addition to the DEER experiment. Shaped pulses offer an increased excitation bandwidth and the possibility to precisely adjust pulse parameters, which is beneficial especially for demanding biological samples. We have noticed that on our home built W-band spectrometer, the dead-time free 4-pulse DEER sequence with chirped pump pulses suffers from distortions at the end of the DEER trace. Although minor, these are crucial for Gd(III)-Gd(III) DEER where the modulation depth is on the order of a few percent. Here we present a modified DEER sequence—referred to as reversed DEER (rDEER)—that circumvents the coherence pathway which gives rise to the distortion. We compare the rDEER (with two chirped pump pulses) performance values to regular 4-pulse DEER with one monochromatic as well as two chirped pulses and investigate the source of the distortion. We demonstrate the applicability and effectivity of rDEER on three systems, ubiquitin labeled with Gd(III)-DOTA-maleimide (DOTA, 1,4,7,10-Tetraazacyclododecane-1,4,7,10-tetraacetic acid) or with Gd(III)-DO3A (DO3A, 1,4,7,10-Tetraazacyclododecane-1,4,7-triyl) triacetic acid) and the multidrug transporter MdfA, labeled with a Gd(III)-C2 tag, and report an increase in the signal-to-noise ratio in the range of 3 to 7 when comparing the rDEER with two chirped pump pulses to standard 4-pulse DEER.

Highlights

  • Double electron-electron resonance (DEER, called Pulsed Electron Double Resonance, PELDOR) is an Electron Paramagnetic Resonance (EPR) method that measures the dipolar interaction between two coupled spins and has become a routine method for structural biology applications [1]

  • We demonstrate and compare the results obtained with rDEER with those obtained from regular DEER and regular DEER with chirp pump pulses on human ubiquitin labeled with Gd(III)-DOTA-maleimide (DOTA, 1,4,7,10-Tetraazacyclododecane-1,4,7,10-tetraacetic acid) and Gd(III)-DO3A (DO3A, (DO3A, 1,4,7,10-Tetraazacyclododecane-1,4,7-triyl) triacetic acid) [28], as well as the multidrug antiporter MdfA [46,47,48], labeled with Gd(III)-C2 [49], with different EPR and Gd(III)-Gd(III) DEER characteristics

  • In order to demonstrate the performance of the rDEER sequence, we chose three samples— (A) Ubiquitin D39C/E64C doubly labeled with Gd(III)-DOTA-maleimide (Ubi-DOTA-M-Gd), (B) Ubiquitin D39C/E64C doubly labeled with Gd(III)-DO3A (Ubi-DO3A-Gd) [28] and (C) MdfA A163C/V307C doubly labeled with Gd(III)-C2 (MdfA-C2-Gd) [49]—to serve as model systems

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Summary

Introduction

Double electron-electron resonance (DEER, called Pulsed Electron Double Resonance, PELDOR) is an Electron Paramagnetic Resonance (EPR) method that measures the dipolar interaction between two (or potentially more) coupled spins and has become a routine method for structural biology applications [1]. We recently presented an AWG setup at the W-band where we reported signal to noise ratio (SNR) improvements for Gd(III)-Gd(III) DEER with one chirp pump pulse by a factor of 2–3.3, meaning a significant reduction in the experiment run-time by a factor of 4–10 [45]. While not a significant problem with the past setup [45], our efforts in increasing SNR with the new setup were limited by a distortion at the end of the DEER time trace that required the extension of the DEER evolution time, τ2 (refer to Figure 1 for an explanation of the symbols used) by almost 1 μs This requires discarding the last microsecond, reducing the effective SNR of the experiment. We demonstrate and compare the results obtained with rDEER with those obtained from regular DEER and regular DEER with chirp pump pulses on human ubiquitin labeled with Gd(III)-DOTA-maleimide (DOTA, 1,4,7,10-Tetraazacyclododecane-1,4,7,10-tetraacetic acid) and Gd(III)-DO3A (DO3A, (DO3A, 1,4,7,10-Tetraazacyclododecane-1,4,7-triyl) triacetic acid) [28], as well as the multidrug antiporter MdfA [46,47,48], labeled with Gd(III)-C2 [49] (for the chemical structure of the spin labels, see Figure 2), with different EPR and Gd(III)-Gd(III) DEER characteristics

Results
Discussion
Sample Preparation
Spectroscopy
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