The Kinetics of the Hydrogen/Deuterium Exchange of Epidermal Growth Factor Receptor Ligands

Abstract

Listen

Translate article

Five highly homologous epidermal growth factor receptor ligands were studied by mass spectral analysis, hydrogen/deuterium (H/D) exchange via attenuated total reflectance Fourier transform-infrared spectroscopy, and two-dimensional correlation analysis. These studies were performed to determine the order of events during the exchange process, the extent of H/D exchange, and associated kinetics of exchange for a comparative analysis of these ligands. Furthermore, the secondary structure composition of amphiregulin (AR) and heparin-binding-epidermal growth factor (HB-EGF) was determined. All ligands were found to have similar contributions of 310-helix and random coil with varying contributions of β-sheets and β-turns. The extent of exchange was 40%, 65%, 55%, 65%, and 98% for EGF, transforming growth factor-α (TGF-α), AR, HB-EGF, and epiregulin (ER), respectively. The rate constants were determined and classified as fast, intermediate, and slow: for EGF the 0.20min−1 (Tyr), 0.09min−1 (Arg, β-turns), and 1.88×10−3min−1 (β-sheets and 310-helix); and for TGF-α 0.91min−1 (Tyr), 0.27min−1 (Arg, β-turns), and 1.41×10−4min−1 (β-sheets). The time constants for AR 0.47min−1 (Tyr), 0.04min−1 (Arg), and 1.00×10−4min−1 (buried 310-helix, β-turns, and β-sheets); for HB-EGF 0.89min−1 (Tyr), 0.14min−1 (Arg and 310-helix), and 1.00×10−3min−1 (buried 310-helix, β-sheets, and β-turns); and for epiregulin 0.16min−1 (Tyr), 0.03min−1 (Arg), and 1.00×10−4min−1 (310-helix and β-sheets). These results provide essential information toward understanding secondary structure, H/D exchange kinetics, and solvation of these epidermal growth factor receptor ligands in their unbound state.