A Closed-Form Expression for Analysis of Dark State Exchange Saturation Transfer (DEST) NMR Experiments

Closed-form expressions for the analysis of Dark state Exchange Saturation Transfer (DEST) NMR experiments, a powerful experimental tool for characterizing exchange processes involving the interaction of NMR visible species with very high molecular weight partners, is presented. Essentially identical exchange and relaxation parameters are derived from the analytical and numerical best fits of the DEST profiles obtained for a protein construct derived from huntingtin exon-1, comprising the N-terminal amphiphilic sequence followed by a seven-residue glutamine repeat, htt<sup>NT</sup>Q<sub>7</sub>, in the presence of small (SUV) and large (LUV) unilamellar lipid vesicles. The use of analytical expressions significantly speeds up the fitting of experimental DEST profiles to a two-state exchange model and simplifies the analysis of the DEST effects.

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Publication Details

Journal
The Journal of Physical Chemistry Letters
Published
2024-10-28
DOI
https://doi.org/10.1021/acs.jpclett.4c02509
Citations
4
Primary Topic
Electron Spin Resonance Studies
Type
article
Field-Weighted Citation Impact
2.65

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article

A Closed-Form Expression for Analysis of Dark State Exchange Saturation Transfer (DEST) NMR Experiments

G. Marius Clore, Vitali Tugarinov, Francesco Torricella
4 citations
The Journal of Physical Chemistry Letters
Electron Spin Resonance Studies
2.65
article

A Closed-Form Expression for Analysis of Dark State Exchange Saturation Transfer (DEST) NMR Experiments

G. Marius Clore, Vitali Tugarinov, Francesco Torricella
article en
4 citations

Abstract

Closed-form expressions for the analysis of Dark state Exchange Saturation Transfer (DEST) NMR experiments, a powerful experimental tool for characterizing exchange processes involving the interaction of NMR visible species with very high molecular weight partners, is presented. Essentially identical exchange and relaxation parameters are derived from the analytical and numerical best fits of the DEST profiles obtained for a protein construct derived from huntingtin exon-1, comprising the N-terminal amphiphilic sequence followed by a seven-residue glutamine repeat, htt<sup>NT</sup>Q<sub>7</sub>, in the presence of small (SUV) and large (LUV) unilamellar lipid vesicles. The use of analytical expressions significantly speeds up the fitting of experimental DEST profiles to a two-state exchange model and simplifies the analysis of the DEST effects.

The Journal of Physical Chemistry LettersVol. 15(44)
National Institutes of Health (US), National Institute of Diabetes and Digestive and Kidney Diseases (US)
National Institute of Diabetes and Digestive and Kidney Diseases
Openalex Percentile: Top 9%
Electron Spin Resonance Studies
2.65
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A Closed-Form Expression for Analysis of Dark State Exchange Saturation Transfer (DEST) NMR Experiments — G. Marius Clore, Vitali Tugarinov, et al. · The Journal of Physical Chemistry Letters (2024) | TGRS Research Map | TGRS