Spins Afar─Long-Range Pulse Dipolar EPR Spectroscopy Uncovers Curvature in TRIM25’s Coiled Coil

Abstract Pulse Dipolar Electron Paramagnetic Resonance Spectroscopy (PDS) is a powerful method for determining nanometer distances in biomolecular systems. This methodology has been successfully used to validate structure hypotheses and to identify disorder. However, inherent distance limitations are under-explored. Many challenging biomolecular applications require long distance information, driving the need for a benchmarking study. We demonstrate distances up to 10.5 nm in TRIM25 reliably extracted from data obtained under standard sample conditions. By protein perdeuteration accurate distance measurements up to 17.3 nm were enabled. Enhancing sensitivity through optimization of the measurement and sample preparation conditions the achievable dipolar evolution time was extended to 150 μs. Thus, distances close to 20 nm should become experimentally accessible, highlighting the potential of advanced PDS methodologies for probing previously inaccessible long-range structural information in complex systems.

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Publication Details

Journal
The Journal of Physical Chemistry Letters
Published
2026-10-05
DOI
https://doi.org/10.1021/acs.jpclett.6c02671
Primary Topic
Electron Spin Resonance Studies
Type
article
Field-Weighted Citation Impact
0.00
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article

Spins Afar─Long-Range Pulse Dipolar EPR Spectroscopy Uncovers Curvature in TRIM25’s Coiled Coil

D. Norman, Bela E. Bode, Katrin Ackermann, Aisika Chakraborty et al.
The Journal of Physical Chemistry Letters
Electron Spin Resonance Studies
article

Spins Afar─Long-Range Pulse Dipolar EPR Spectroscopy Uncovers Curvature in TRIM25’s Coiled Coil

D. Norman, Bela E. Bode, Katrin Ackermann, Aisika Chakraborty, Yannik Limbach
article en

Abstract

Abstract Pulse Dipolar Electron Paramagnetic Resonance Spectroscopy (PDS) is a powerful method for determining nanometer distances in biomolecular systems. This methodology has been successfully used to validate structure hypotheses and to identify disorder. However, inherent distance limitations are under-explored. Many challenging biomolecular applications require long distance information, driving the need for a benchmarking study. We demonstrate distances up to 10.5 nm in TRIM25 reliably extracted from data obtained under standard sample conditions. By protein perdeuteration accurate distance measurements up to 17.3 nm were enabled. Enhancing sensitivity through optimization of the measurement and sample preparation conditions the achievable dipolar evolution time was extended to 150 μs. Thus, distances close to 20 nm should become experimentally accessible, highlighting the potential of advanced PDS methodologies for probing previously inaccessible long-range structural information in complex systems.

The Journal of Physical Chemistry Letters
University of Bonn (DE), University of St Andrews (GB), University of Dundee (GB)
Openalex Percentile: Top 17%
Electron Spin Resonance Studies
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Spins Afar─Long-Range Pulse Dipolar EPR Spectroscopy Uncovers Curvature in TRIM25’s Coiled Coil — D. Norman, Bela E. Bode, et al. · The Journal of Physical Chemistry Letters (2026) | TGRS Research Map | TGRS