| Literature DB >> 29227566 |
Ganesan Karthikeyan1, Alessio Bonucci2, Gilles Casano1, Guillaume Gerbaud2, Sébastien Abel1, Virginie Thomé3, Laurent Kodjabachian3, Axel Magalon4, Bruno Guigliarelli2, Valérie Belle2, Olivier Ouari1, Elisabetta Mileo2.
Abstract
Approaching protein structural dynamics and protein-protein interactions in the cellular environment is a fundamental challenge. Owing to its absolute sensitivity and to its selectivity to paramagnetic species, site-directed spin labeling (SDSL) combined with electron paramagnetic resonance (EPR) has the potential to evolve into an efficient method to follow conformational changes in proteins directly inside cells. Until now, the use of nitroxide-based spin labels for in-cell studies has represented a major hurdle because of their short persistence in the cellular context. The design and synthesis of the first maleimido-proxyl-based spin label (M-TETPO) resistant towards reduction and being efficient to probe protein dynamics by continuous wave and pulsed EPR is presented. In particular, the extended lifetime of M-TETPO enabled the study of structural features of a chaperone in the absence and presence of its binding partner at endogenous concentration directly inside cells.Entities:
Keywords: EPR spectroscopy; chaperone proteins; in-cell spectroscopy; nitroxide; site-directed spin labeling
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Year: 2018 PMID: 29227566 DOI: 10.1002/anie.201710184
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336