The equilibrium distribution of small molecules (ligands) between binding agents in heterogeneous media is an important property that determines their activity. Heterogeneous systems containing proteins and lipid membranes are particularly relevant due to their prevalence in biological systems, and their importance to ligand distribution, which, in turn, is crucial to ligand’s availability and biological activity. In this work, we review several approaches and formalisms for the analysis of the equilibrium distribution of ligands in the presence of proteins, lipid membranes, or both. Special attention is given to common pitfalls in the analysis, with the establishment of the validity limits for the distinct approaches. Due to its widespread...
The nonspecific binding of proteins to various biological and non-biological surfaces has limited th...
We analyze the stability of micro-domains of ligand-receptor bonds that mediate the adhesion of biol...
The dynamic behavior of the concentration profiles of a single protein in the pore solution and the ...
The equilibrium distribution of small molecules (ligands) between binding agents in heterogeneous me...
The equilibrium distribution of small molecules (ligands) between binding agents in heterogeneous me...
We examine the binding of fluorescent ligands to proteins by analyzing the fluctuation amplitude g(0...
The theory of receptor–ligand binding equilibria has long been well-established in biochemistry, and...
Many systems in biology rely on binding of ligands to target proteins in a single high-affinity conf...
The work on hand deals with different topics within the theory of ligand binding. The introductory ...
Specific interactions of lipids with membrane proteins contribute to protein stability and function....
Explicit expressions are derived which determine the equilibrium composition of mixtures comprising ...
AbstractDepth-dependent fluorescence quenching by lipid-attached quenchers (e.g., bromine atoms and ...
Intramolecular interaction networks in proteins are responsible for heterotropic ligand binding coop...
International audienceUnderstanding the interplay between molecules and lipid membranes is fundament...
AbstractWe examine the binding of fluorescent ligands to proteins by analyzing the fluctuation ampli...
The nonspecific binding of proteins to various biological and non-biological surfaces has limited th...
We analyze the stability of micro-domains of ligand-receptor bonds that mediate the adhesion of biol...
The dynamic behavior of the concentration profiles of a single protein in the pore solution and the ...
The equilibrium distribution of small molecules (ligands) between binding agents in heterogeneous me...
The equilibrium distribution of small molecules (ligands) between binding agents in heterogeneous me...
We examine the binding of fluorescent ligands to proteins by analyzing the fluctuation amplitude g(0...
The theory of receptor–ligand binding equilibria has long been well-established in biochemistry, and...
Many systems in biology rely on binding of ligands to target proteins in a single high-affinity conf...
The work on hand deals with different topics within the theory of ligand binding. The introductory ...
Specific interactions of lipids with membrane proteins contribute to protein stability and function....
Explicit expressions are derived which determine the equilibrium composition of mixtures comprising ...
AbstractDepth-dependent fluorescence quenching by lipid-attached quenchers (e.g., bromine atoms and ...
Intramolecular interaction networks in proteins are responsible for heterotropic ligand binding coop...
International audienceUnderstanding the interplay between molecules and lipid membranes is fundament...
AbstractWe examine the binding of fluorescent ligands to proteins by analyzing the fluctuation ampli...
The nonspecific binding of proteins to various biological and non-biological surfaces has limited th...
We analyze the stability of micro-domains of ligand-receptor bonds that mediate the adhesion of biol...
The dynamic behavior of the concentration profiles of a single protein in the pore solution and the ...