Biochemistry, Biophysics, and Structural Biology Commons^™

Quantifying The Differences In Binding Affinity Of Reduced Glutathione For Glutathione S-Transferase At Ph 6.5 And 8.5 Using Isothermal Titration Calorimetry, Clay P. Renshaw Jr., Ronald K. Gary

McNair Poster Presentations

The binding affinity between an enzyme and its substrate is often dependent on the pH of the local environment. Knowing the pH at which reduced glutathione (GSH) binds with the highest affinity to the enzyme glutathione S-transferase (GST) is useful for determining the optimal pH for purification of GST-fusion proteins during GST-affinity chromatography. In this study, GST of the species Schistosoma japonicum was purified, quantified, and utilized to study its binding interaction with GSH at pH 6.5 and 8.5 via isothermal titration calorimetry (ITC). After protein expression, extraction, and purification, the GST concentration was quantified using Qubit^TM fluorometry. …