When disengaged interactions within a receptor are turned on by its guest, these intrahost interactions will contribute to the overall binding energy. Although such receptors are common in biology, their synthetic mimics are rare and difficult to design. By engineering conflictory requirements between intrareceptor electrostatic and hydrophobic interactions, we enabled complementary guests to eliminate the “electrostatic frustration” within the host and turn on the intrahost interactions. The result was a binding constant of Ka \u3e105 M–1 from ammonium–carboxylate salt bridges that typically function poorly in water. These cooperatively enhanced receptors displayed excellent selectivity in binding, despite a large degree of conformational ...
When direct host–guest binding interactions are weakened by unfavorable solvent competition, guest-t...
Docking algorithms for computer-aided drug discovery and design often ignore or restrain the flexibi...
Bis-polyaza pyridinophane scorpiands bind nucleotides in aqueous medium by 10-100 micromolar affinit...
When disengaged interactions within a receptor are turned on by its guest, these intrahost interacti...
In theory, a perfectly rigid receptor will probably be an unbeatable binder. However, rigidity may n...
The present impact of supramolecular chemistry in biology is not as large as it could be. The affini...
Glutamate-functionalized oligocholate foldamers bound Zn(OAc)2, guanidine, and even amine compounds ...
Cooperativity (homotropic allostery) is the primary mechanism by which evolution steepens the bindin...
AbstractBackground: Molecular recognition processes are ubiquitous in nature: substrate binding by e...
Structural and thermodynamic data are presented on the binding properties of anion receptors contain...
Metal complexes of the amino acid, 4,4[superscript]\u27-phosphinylidine bis phenylalanine (PBP*, 1),...
Biomolecular and artificial receptors are typically designed to exploit the hydrophobic effect in or...
A new class of high-symmetry, water-soluble receptors has been synthesized. The enantiomerically pur...
Structures of integral membrane receptors provide valuable models for drug–receptor interactions acr...
Synthetic supramolecular complexes provide an opportunity for quantitative systematic exploration of...
When direct host–guest binding interactions are weakened by unfavorable solvent competition, guest-t...
Docking algorithms for computer-aided drug discovery and design often ignore or restrain the flexibi...
Bis-polyaza pyridinophane scorpiands bind nucleotides in aqueous medium by 10-100 micromolar affinit...
When disengaged interactions within a receptor are turned on by its guest, these intrahost interacti...
In theory, a perfectly rigid receptor will probably be an unbeatable binder. However, rigidity may n...
The present impact of supramolecular chemistry in biology is not as large as it could be. The affini...
Glutamate-functionalized oligocholate foldamers bound Zn(OAc)2, guanidine, and even amine compounds ...
Cooperativity (homotropic allostery) is the primary mechanism by which evolution steepens the bindin...
AbstractBackground: Molecular recognition processes are ubiquitous in nature: substrate binding by e...
Structural and thermodynamic data are presented on the binding properties of anion receptors contain...
Metal complexes of the amino acid, 4,4[superscript]\u27-phosphinylidine bis phenylalanine (PBP*, 1),...
Biomolecular and artificial receptors are typically designed to exploit the hydrophobic effect in or...
A new class of high-symmetry, water-soluble receptors has been synthesized. The enantiomerically pur...
Structures of integral membrane receptors provide valuable models for drug–receptor interactions acr...
Synthetic supramolecular complexes provide an opportunity for quantitative systematic exploration of...
When direct host–guest binding interactions are weakened by unfavorable solvent competition, guest-t...
Docking algorithms for computer-aided drug discovery and design often ignore or restrain the flexibi...
Bis-polyaza pyridinophane scorpiands bind nucleotides in aqueous medium by 10-100 micromolar affinit...