Characterization of the transition state of Lysozyme unfolding. I. Effect of protein-solvent interactions on the transition state

✍ Scribed by Shin-Ichi Segawa; Mitsuru Sugihara

• Publisher: Wiley (John Wiley & Sons)
• Year: 2007
• Tongue: English
• Weight: 886 KB
• Volume: 23
• Category: Article
• ISSN: 0006-3525
• DOI: 10.1002/bip.360231122

✦ Synopsis

The influence of proline cis-trans isomerization on the kinetics of lysozyme unfolding was examined carefully according to the theory of Hagerman and Baldwin "1976) Biochemistry 15, 1462-14731. As a result, the kinetics of lysozyme unfolding was found to follow the two-state transition model well. The temperature dependencies of k,, and kf over a wide temperature range showed that Act, = 0 and ACf = -6.7 kJ K-' mol-l in solutions of different concentrations of GuHC1. The data observed in solutions containing other denaturants also supported the conclusion that hour is nearly equal to zero. The activation enthalpies of unfolding (AHi,) were observed at various concentrations of several kinds of denaturants. They were independent of species and concentrations of denaturants (AH?,f = 200 kJ mol-9. These facts indicate that the aspect of interaction between protein and different kinds of solvent molecules varies only slightly during the unfolding to the transition state, that is, the transition state is at compact as the native one. Therefore, it is also suggested that AH?,, of 200 kJ mol-1 is primarily required for the disruption of long-range interactions among different structural domains through a subtle conformational change. We compared the effects of several kinds of denaturants on the unfolding rate. The addition of PrOH more remarkably increases the unfolding rate than do other hydrophilic denaturants. This is probably because PrOH molecules can penetrate into the hydrophobic core of lysozyme, but hydrophilic reagents cannot because of the compactness of the transition state.