The association is the first phase in a biomolecular interaction experiment. Binding occurs when analyte and ligand collide due to diffusion, and when the collision has the correct orientation and enough energy. The rate of association (number of binding events per unit of time) equals:
Once binding has occurred, the ligand and analyte remain bound together for a random amount of time. The rate of dissociation (number of dissociation events per unit of time) equals:
The probability of dissociation is the same every instant of time. The analyte does not "know" how long it has been bound to the ligand. After dissociation, the ligand and analyte are the same as they were before binding. If either analyte or ligand is chemically modified, then the binding does not follow the law of mass action (1, 2).
The reaction between immobilized ligand (L) and an analyte (A) can be assumed to follow a pseudo first order kinetics (3, 4, 6). During the association phase, the complex [LA] increases as a function of time according to:
The association rate constant ka describes the rate of complex formation, i.e. the number of LA complexes formed per second in a one molar solution of L and A. The units of ka are M-1s-1 and are typically between 1.103 and 1.107 in biological systems.
The dissociation rate constant kd describes the stability of the complex, i.e. the fraction of complexes that decays per second. The unit of kd is s-1 and is typically between 1.10-1 and 1.10-6 in biological systems. A kd of 1.10-2 s-1 = 0.01 s-1. This means that 1 percent of the complexes decay per second (5).
Fitting the kinetic equation is not an easy task. One way is the transformation of the kinetic equation to a so called integrated rate equation, which can be resolved by computer programs.
Although simple rate equations are easily intergrated, the more complex (e.g. with mass transport parameters) are not. The more complex rate equations are resolved by numeric calculations. In both cases, the programs try to find the parameters that describe the data the best.
|1||GraphPad Prism; (1998).|
|2||BIACORE AB; BIACORE Technology Handbook; (1998).|
|3||Chaiken, I. M. and et al; Analytical Biochemistry;212: 457-468; (1993).|
|4||Jonsson, U. et all; Real-time biospecific interaction analysis using surface plasmon resonance and a sensor chip technology; Biotechniques;11: 620-627; (1991).|
|5||Elwing, H.; Protein absorption and ellipsometry in biomaterial research; Biomaterials;19: 397-406; (1998).|
|6||Bjorquist, P. and Bostrom, S.; Determination of the kinetic constants of tissue factor/factor VII/factor VIIA and antithrombin/heparin using surface plasmon resonance; Thromb.Res.;85: 225-236; (1-2-1997).|