A general model of multivalent binding with ligands of heterotypic subunits and multiple surface receptors
DOI10.1016/J.MBS.2021.108714zbMATH Open1480.92083OpenAlexW3207462472MaRDI QIDQ2066471FDOQ2066471
Authors: Zhixin Cyrillus Tan, Aaron S. Meyer
Publication date: 14 January 2022
Published in: Mathematical Biosciences (Search for Journal in Brave)
Full work available at URL: https://doi.org/10.1016/j.mbs.2021.108714
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combinatoricsmultivalent bindingprotein-protein interactionscell surface reactionsgeneral binding modelreceptor-ligand interactions
Cites Work
- Receptor clustering on a cell surface. I. Theory of receptor cross- linking by ligands bearing two chemically identical functional groups
- Scaffold-mediated nucleation of protein signaling complexes: elementary principles
- Receptor clustering on a cell surface. III. Theory of receptor cross- linking by multivalent ligands: Description by ligand states
- Receptor clustering on a cell surface. II. Theory of receptor cross- linking by ligands bearing two chemically distinct functional groups
Cited In (11)
- Computational methods for fitting statistical distribution models of multi-site binding equilibria
- Ligand-induced coupling versus receptor pre-association: cellular automaton simulations of FGF-2 binding
- Allostery in oligomeric receptor models
- Theoretical quantification of the polyvalent binding of nanoparticles coated with peptide-major histocompatibility complex to T cell receptor-nanoclusters
- A method to calculate binding equilibrium concentrations in the allosteric ternary complex model that supports ligand depletion
- 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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