A general model of multivalent binding with ligands of heterotypic subunits and multiple surface receptors
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Publication:2066471
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Cites work
- Receptor clustering on a cell surface. I. Theory of receptor cross- linking by ligands bearing two chemically identical functional groups
- Receptor clustering on a cell surface. II. Theory of receptor cross- linking by ligands bearing two chemically distinct functional groups
- Receptor clustering on a cell surface. III. Theory of receptor cross- linking by multivalent ligands: Description by ligand states
- Scaffold-mediated nucleation of protein signaling complexes: elementary principles
Cited in
(11)- Ligand-induced coupling versus receptor pre-association: cellular automaton simulations of FGF-2 binding
- Computational methods for fitting statistical distribution models of multi-site binding equilibria
- Allostery in oligomeric receptor models
- A method to calculate binding equilibrium concentrations in the allosteric ternary complex model that supports ligand depletion
- Theoretical quantification of the polyvalent binding of nanoparticles coated with peptide-major histocompatibility complex to T cell receptor-nanoclusters
- Why ligand cross-reactivity is high within peptide recognition domain families? A case study on human \(c\)-src SH3 domain
- Equilibrium binding of multivalent ligands to cells: Effects of cell and receptor density
- Impact of plasma-protein binding on receptor occupancy: an analytical description
- Generalized concentration addition for ligands that bind to homodimers
- On the interaction of different types of ligands binding to the same molecule part II: systems with \(n\) to 2 and \(n\) to 3 binding sites
- Wilder continua and their subfamilies as coanalytic absorbers
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