Abstract
The design of new strong and selective binders is a key step towards the development of new sensing devices and effective drugs. Both affinity and selectivity can be increased through chelation and here we theoretically explore the possibility of coupling two binders through a flexible linker. We prove the enhanced ability of double binders of keeping their target with a simple model where a polymer composed by hard spheres interacts with a spherical macromolecule, such as a protein, through two sticky spots. By Monte Carlo simulations and thermodynamic integration we show the chelating effect to hold for coupling polymers whose radius of gyration is comparable to size of the chelated particle. We show the binding free energy of flexible double binders to be higher than that of two single binders and to be maximized when the binding sites are at distances comparable to the mean free polymer end-to-end distance. The affinity of two coupled binders is therefore predicted to increase non linearly and in turn, by targeting two non-equivalent binding sites, this will lead to higher selectivity.
Highlights
Coupling the binding moieties through long polymeric flexible linkers is advantageous due to their low cost, ease of synthesis, and large variety of structural and chemical properties such as solubility, hydrophobicity, reactivity they have
When discussing polymer adsorption on a curved surface, three behavioral regimes can be identified depending on the relative size between the polymer and the particle[22]: (i) the size of the nanoparticle is larger than the radius of gyration (Rg) of the polymer, (ii) they are comparable, (iii) the size of the nanoparticle is far smaller
While making clear that the statistical quantities are derived under non equilibrium simulations, we will discuss the results according to standard equilibrium thermodynamic language keeping in mind that the statistical quantities calculated over these states will not be the thermodynamic ones but will be non-equilibrium quantities
Summary
Coupling the binding moieties through long polymeric flexible linkers is advantageous due to their low cost, ease of synthesis, and large variety of structural and chemical properties such as solubility, hydrophobicity, reactivity they have. By running a set of simulations by switching off the beads-protein hard-sphere potential, for all cases the excluded volume effect is that of moving the transitions towards lower temperatures and bringing all the CV curves closer to each other (Fig. 3b,c).
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