Biochemistry
Given a protein-ligand complex concentration of 0.5 mM and a free protein concentration of 0.5 mM, calculate the fractional saturation.
How does the fractional saturation equation resemble the Michaelis-Menten equation?
Why is the dissociation equilibrium constant, Kd, significant in protein-ligand interactions?
What is the maximum value of fractional saturation, theta?
If Protein A has a Kd of 0.1 mM and Protein B has a Kd of 0.5 mM, which protein has a higher affinity for its ligand?
In a clinical setting, why might a researcher be interested in determining the Kd value of a drug-protein interaction?
If the concentration of protein-ligand complex is 0.3 mM and the concentration of free protein is 0.7 mM, what is the fractional saturation?