Hydration and H/D exchange-dependent infrared signatures of the GCN4 leucine zipper
Bhuvanendran, H.; Brunner, C. M.; Kempf, H.; Moro, J. L.; Roubieu, E.; Turbant, F.; Mateus, A.; Lin, H.; Das, L.; Malyshev, D.; Johns, B.; Parracino, A.; Pastore, A.; Peters, J.; Cortajarena, A. L.; Zanetti Polzi, L.; Maccaferri, N.
Show abstract
Attenuated total reflectance Fourier-transform infrared (ATR-FTIR) spectroscopy of proteins in aqueous solution is often limited by water absorption and other optical artifacts. To overcome these limitations, we evaluated the structural features and hydrogen-deuterium exchange (HDX) kinetics of the -helical protein GCN4 in both hydrated (wet) and vacuum-dried (dry) states. While solvent heavily mask the second-derivative spectra of wet samples, vacuum drying yielded a thin, protein-rich film on the ATR crystal, significantly enhancing the signal-to-noise ratio and resolving the protein features without altering the native structure. Dry-state analysis clearly resolved the Amide I, Amide II, and deuterium-shifted Amide II' (1450 cm-1) bands. Notably, second-derivative analysis of the dry spectra of the HDX samples revealed a bimodal Amide I distribution consisting of a stationary band at 1653 cm-1 from the solvent-inaccessible regions and an isotopically sensitive band shifting from 1648 cm-1 to 1644 cm-1 from solvent-accessible regions. These results demonstrate that vacuum-dried ATR-FTIR spectroscopy effectively eliminates solvent masking, providing the spectral clarity required to resolve discrete -helical sub-populations after deuteration.
Matching journals
The top 8 journals account for 50% of the predicted probability mass.