The determination of the p Ka of histidine residues in proteins by Raman difference spectroscopy

Abstract

Sensitive Raman difference spectroscopy was used to monitor the protonation and deprotonation of histidine residues in apo-transferrin. We have shown previously that the behavior of small molecules and/or small molecular groups bound to proteins or other large macromolecules can be studied by Raman difference spectroscopy (Yue, K.T. et al. (1989) J. Raman Spectrosc. 20, 541–545). Using this method, we have measured the Raman difference spectra of human transrferin at different pH values with respect to pH 8.9, titrating its various histidine residues. About 12±2 of the 19 residues were titrated. The pH difference spectrum of transferrin obtained is very similar to that of histidine in solution, but with clear differences in the 1200–1400 cm −1 region. A titration curve with p K a of 6.08 ± 0.01 fit the data of histidine in solution and a value of 6.56 ± 0.02 was found for the average value of the 12 histidine residues inside transferrin. The technique has enough sensitivity at present to monitor a single histidine residue in a 130 kDa molecule and to determine the titration curve of one residue in a 40 kDa protein.