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Abstract
Recent sensitivity enhancements in pulse dipolar EPR spectroscopy (PDS) have afforded distance measurements at submicromolar spin concentrations. This development opens the path for new science, as more biomolecular systems can be investigated at their respective physiological concentrations. Here, we demonstrate that the combination of orthogonal spin labelling using CuII ions and trityl yields a more than 3-fold sensitivity increase compared to the established CuII-nitroxide labelling strategy. Application of the recently developed variable-time RIDME method yields a further approximately 2.5-fold increase compared to the commonly used constant-time RIDME. This overall increase in sensitivity of almost an order of magnitude makes distance measurements in the range of 3 nm with protein concentrations as low as 10 nM feasible, more than two times lower than previously reported. We expect that experiments at single digit nanomolar concentrations are imminent, which has the potential to transform biological PDS applications.
Original language | English |
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Pages (from-to) | 1455-1461 |
Number of pages | 7 |
Journal | The Journal of Physical Chemistry Letters |
Volume | 15 |
Early online date | 31 Jan 2024 |
DOIs | |
Publication status | E-pub ahead of print - 31 Jan 2024 |
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Dive into the research topics of 'Pulse dipolar electron paramagnetic resonance spectroscopy distance measurements at low nanomolar concentrations: the CuII-trityl case'. Together they form a unique fingerprint.-
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Cryogen-free arbitrary waveform EPR: Cryogen-free arbitrary waveform EPR for structural Biology and Biophysics
Bode, B. E. (PI), Lovett, J. E. (CoI), Pliotas, C. (CoI), Schwarz-Linek, U. (CoI), Smith, G. M. (CoI), Stewart, A. J. (CoI) & White, M. (CoI)
1/05/18 → 30/04/19
Project: Standard
Datasets
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Pulse Dipolar Electron Paramagnetic Resonance Spectroscopy Distance Measurements at Low Nanomolar Concentrations: the Cu(II)-Trityl Case
Ackermann, K. (Creator), Heubach, C. (Creator), Schiemann, O. (Creator) & Bode, B. E. (Creator), University of St Andrews, 2023
DOI: 10.17630/4a648038-3e79-4eaf-a185-f6721e4060fa
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