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• W4323920595 abstract "Studies of protein structure and dynamics are usually carried out in dilute buffer solutions, conditions that differ significantly from the crowded environment in the cell. The double electron-electron resonance (DEER) technique can track proteins' conformations in the cell by providing distance distributions between two attached spin labels. This technique, however, cannot access distances below 1.8 nm. Here, we show that GdIII -19 F Mims electron-nuclear double resonance (ENDOR) measurements can cover part of this short range. Low temperature solution and in-cell ENDOR measurements, complemented with room temperature solution and in-cell GdIII -19 F PRE (paramagnetic relaxation enhancement) NMR measurements, were performed on fluorinated GB1 and ubiquitin (Ub), spin-labeled with rigid GdIII tags. The proteins were delivered into human cells via electroporation. The solution and in-cell derived GdIII -19 F distances were essentially identical and lie in the 1-1.5 nm range revealing that both, GB1 and Ub, retained their overall structure in the GdIII and 19 F regions in the cell." @default.
• W4323920595 created "2023-03-12" @default.
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• W4323920595 date "2023-04-12" @default.
• W4323920595 modified "2023-10-18" @default.
• W4323920595 title "Gd^III‐¹⁹F Distance Measurements for Proteins in Cells by Electron‐Nuclear Double Resonance" @default.
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• W4323920595 doi "https://doi.org/10.1002/anie.202218780" @default.
• W4323920595 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/36905181" @default.
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