AbstractThe dissociation constant for the binding of a spectroscopically invisible or non-radioactive ligand to its protein receptor can be determined in a competition experiment by using a structural analog that contains a reporter group. Many plotting and numerical analysis methods have been developed to calculate the binding constant of unlabeled ligand from the displacement experiments. However, a common problem with these plotting methods is that the equation transformations inevitably result in non-standard error distribution, and thus simple linear regression can not be used to extract correct values for the parameters. In the case of the numerical analysis methods, one would be faced with the possible existence of multiple solutions...
ABSTRACT: Small molecules can be discovered or engineered to bind tightly to biologically relevant p...
Previous methods to determine equilibrium binding constants of proteins interacting with ligands inc...
The reversible combination of a ligand with specific sites on the surface of a receptor is one of th...
AbstractFor the most frequently used two-site model, an exact binding equation is presented in terms...
The physiological role played by protein-ligand recognition has motivated the development of several...
For ligand - biomacromolecule titration experiments it has been traditional practice to extract para...
AbstractA comparative analysis is provided of rigorous and approximate methods for calculating absol...
AbstractIt is widely accepted that the binding constant of a receptor and ligand can be written as a...
BACKGROUND: The affinities of DNA binding proteins for target sites can be used to model the regulat...
AbstractThere is often an interest in knowing, for a given ligand concentration, how many protein mo...
The prediction of the binding affinity between a protein and ligands is one of the most challenging ...
Within the last years, for several ligands, binding to G protein-coupled receptors or other target p...
International audienceThe interaction between ligands and receptors is often described in terms of 5...
In this dissertation, a theoretical model is presented for the binding of flexible ligands to protei...
Recent advances in proteomic screening approaches have led to the isolation of a wide variety of bin...
ABSTRACT: Small molecules can be discovered or engineered to bind tightly to biologically relevant p...
Previous methods to determine equilibrium binding constants of proteins interacting with ligands inc...
The reversible combination of a ligand with specific sites on the surface of a receptor is one of th...
AbstractFor the most frequently used two-site model, an exact binding equation is presented in terms...
The physiological role played by protein-ligand recognition has motivated the development of several...
For ligand - biomacromolecule titration experiments it has been traditional practice to extract para...
AbstractA comparative analysis is provided of rigorous and approximate methods for calculating absol...
AbstractIt is widely accepted that the binding constant of a receptor and ligand can be written as a...
BACKGROUND: The affinities of DNA binding proteins for target sites can be used to model the regulat...
AbstractThere is often an interest in knowing, for a given ligand concentration, how many protein mo...
The prediction of the binding affinity between a protein and ligands is one of the most challenging ...
Within the last years, for several ligands, binding to G protein-coupled receptors or other target p...
International audienceThe interaction between ligands and receptors is often described in terms of 5...
In this dissertation, a theoretical model is presented for the binding of flexible ligands to protei...
Recent advances in proteomic screening approaches have led to the isolation of a wide variety of bin...
ABSTRACT: Small molecules can be discovered or engineered to bind tightly to biologically relevant p...
Previous methods to determine equilibrium binding constants of proteins interacting with ligands inc...
The reversible combination of a ligand with specific sites on the surface of a receptor is one of th...