A GdIII-Based Spin Label at the Limits for Linewidth Reduction through Zero-Field Splitting Optimization

The remarkably narrow central line in the electron paramagnetic resonance spectrum and the very weak zero-field splitting (ZFS) make [GdIII(NO3Pic)] ([GdIII(TPATCN)]) an attractive starting point for the development of spin labels. For retaining the narrow line of this parent complex when modifying it with a substituent enabling bioconjugation, alkyl with a somehow remote functional group as a substituent at the picolinate moiety was found to be highly suitable because ZFS stayed weak, even if the threefold axial symmetry was broken. The ZFS is so weak that hyperfine coupling and/or g-value variations noticeably determine the linewidth in Q band and higher fields when the biomolecule is protonated, which is the standard situation, and in W band and higher fields for the protonated complex in a fully deuterated surrounding. Clearly, [NDSE-{GdIII(NO3Pic)}], a spin label targeting the cysteines in a peptide, is at a limit of linewidth narrowing through ZFS minimization. The labeling reaction is highly chemoselective and, applied to a polyproline with two cysteine units, it took no more than a minute at 7 degrees C and pH 7.8. Subsequent disulfide scrambling is very slow and can therefore be prevented. Double electron-electron resonance and relaxation-induced dipolar modulation enhancement applied to the spin-labeled polyproline proved the spin label useful for distance determination in peptides.

Automated summary

The narrow central line and weak zero-field splitting (ZFS) of [GdIII(NO3Pic)] make it an attractive starting point for the development of spin labels. A substituent of alkyl with a remote functional group at the picolinate moiety can retain the narrow line and weak ZFS even with broken axial symmetry. By chemoselective labeling reaction, a spin label targeting cysteines in peptides (NDSE-{GdIII(NO3Pic)}) has been successfully designed for distance determination in peptides.