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AbstractAllosteric cooperativity, which nature uses to improve the sensitivity with which biomolecular receptors respond to small changes in ligand concentration, could likewise be of use in improving the responsiveness of artificial biosystems. Thus motivated, we demonstrate here the rational design of cooperative molecular beacons, a widely employed DNA sensor, using a generalizable population‐shift approach in which we engineer receptors that equilibrate between a low‐affinity state and a high‐affinity state exposing two binding sites. Doing so we achieve cooperativity within error of ideal behavior, greatly steepening the beacon’s binding curve relative to that of the parent receptor. The ability to rationally engineer cooperativity should prove useful in applications such as biosensors, synthetic biology and “smart” biomaterials, in which improved responsiveness is of value.
Models, Molecular, Settore CHIM/01 - CHIMICA ANALITICA, Receptors, Drug, Molecular Conformation, Ligand, Bioengineering, Biocompatible Materials, 612, Biosensing Techniques, cooperative effect, sensors, Ligands, Protein Engineering, DNA; allosterism; cooperative effects; sensors; synthetic biology; Binding Sites; Biocompatible Materials; Biosensing Techniques; DNA; Ligands; Models, Molecular; Molecular Conformation; Protein Engineering; Receptors, Drug, Biosensing Technique, sensor, Models, Receptors, Biocompatible Material, allosterism, Binding Sites, Organic Chemistry, Binding Site, Molecular, DNA, Chemical Sciences, cooperative effects, synthetic biology, Drug, Biotechnology
Models, Molecular, Settore CHIM/01 - CHIMICA ANALITICA, Receptors, Drug, Molecular Conformation, Ligand, Bioengineering, Biocompatible Materials, 612, Biosensing Techniques, cooperative effect, sensors, Ligands, Protein Engineering, DNA; allosterism; cooperative effects; sensors; synthetic biology; Binding Sites; Biocompatible Materials; Biosensing Techniques; DNA; Ligands; Models, Molecular; Molecular Conformation; Protein Engineering; Receptors, Drug, Biosensing Technique, sensor, Models, Receptors, Biocompatible Material, allosterism, Binding Sites, Organic Chemistry, Binding Site, Molecular, DNA, Chemical Sciences, cooperative effects, synthetic biology, Drug, Biotechnology
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