Dynamic Combinatorial Optimization of a Neutral Receptor That Binds Inorganic Anions in Aqueous Solution
- 5 June 2003
- journal article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 125 (26) , 7804-7805
- https://doi.org/10.1021/ja0351589
Abstract
A dynamic combinatorial library of potential anion receptors was generated from a cyclic peptide disulfide dimer and a series of dithiol spacers. Exposing the library to KI or K2SO4 led to the amplification of two new neutral receptors that bind anions through hydrogen bonding with up to micromolar affinity in aqueous solution. Thermodynamic studies suggest that these second-generation receptors outclass the previously described first-generation receptor, largely as a result of a more favorable enthalpy of binding. These results demonstrate that dynamic combinatorial optimization of designed hosts can be a powerful strategy, bringing synthetic receptors that approach the efficiencies of proteins one step closer.Keywords
This publication has 9 references indexed in Scilit:
- Selection and Amplification of a Catalyst from a Dynamic Combinatorial LibraryAngewandte Chemie International Edition in English, 2003
- A Molecular Oyster: A Neutral Anion Receptor Containing Two Cyclopeptide Subunits with a Remarkable Sulfate Affinity in Aqueous SolutionJournal of the American Chemical Society, 2002
- Band Gap Fluorescence from Individual Single-Walled Carbon NanotubesScience, 2002
- How To Synthesize Macrocycles Efficiently by Using Virtual Combinatorial LibrariesChemistry – A European Journal, 2002
- A Cyclic Hexapeptide Containing L ‐Proline and 6‐Aminopicolinic Acid Subunits Binds Anions in WaterAngewandte Chemie International Edition in English, 2001
- In Situ Generation and Screening of a Dynamic Combinatorial Carbohydrate Library against Concanavalin AChemBioChem, 2000
- Use of Molecular Recognition To Drive Chemical Evolution: Mechanisms of an Automated Genetic Algorithm ImplementationChemistry – A European Journal, 1998
- Chemical Evolution: A Model System That Selects and Amplifies a Receptor for the Tripeptide (d)Pro(l)Val(d)ValThe Journal of Organic Chemistry, 1998
- Macrocyclization under thermodynamic control. A theoretical study and its application to the equilibrium cyclooligomerization of .beta.-propiolactoneJournal of the American Chemical Society, 1993