A Trivalent System from Vancomycin· d -Ala- d -Ala with Higher Affinity Than Avidin·Biotin
- 1 May 1998
- journal article
- other
- Published by American Association for the Advancement of Science (AAAS) in Science
- Vol. 280 (5364) , 708-711
- https://doi.org/10.1126/science.280.5364.708
Abstract
Tris(vancomycin carboxamide) binds a trivalent ligand derived fromd-Ala-d-Ala with very high affinity: dissociation constant (K d) ≈ 4 × 10–17 ± 1 × 10–17 M. High-affinity trivalent binding and monovalent binding are fundamentally different. In trivalent (and more generally, polyvalent) binding, dissociation occurs in stages, and its rate can be accelerated by monovalent ligand at sufficiently high concentrations. In monovalent binding, dissociation is determined solely by the rate constant for dissociation and cannot be accelerated by added monomer. Calorimetric measurements for the trivalent system indicate an approximately additive gain in enthalpy relative to the corresponding monomers. This system is one of the most stable organic receptor-ligand pairs involving small molecules that is known. It illustrates the practicality of designing very high-affinity systems based on polyvalency.Keywords
This publication has 20 references indexed in Scilit:
- Tight Binding of a Dimeric Derivative of Vancomycin with Dimeric l-Lys-d-Ala-d-AlaJournal of the American Chemical Society, 1997
- Crystal structure of vancomycinStructure, 1996
- Polyacrylamides Bearing Pendant α-Sialoside Groups Strongly Inhibit Agglutination of Erythrocytes by Influenza Virus: The Strong Inhibition Reflects Enhanced Binding through Cooperative Polyvalent InteractionsJournal of the American Chemical Society, 1996
- Asymmetry in the structure of glycopeptide antibiotic dimers: NMR studies of the ristocetin A complex with a bacterial cell wall analogJournal of the American Chemical Society, 1995
- Microcalorimetry and the molecular recognition of peptides and proteinsPhilosophical Transactions A, 1993
- Kinetics and mechanism of binding of specific peptides to vancomycin and other glycopeptide antibioticsJournal of the American Chemical Society, 1991
- Towards the development of antimicrobial drugs acting by inhibition of pathogen attachment to host cells: A need for polyvalencyFEBS Letters, 1989
- Synthesis of antigenic carbohydrate polymers recognized by lectins and antibodiesJournal of the Chemical Society, Chemical Communications, 1988
- Structure of the glycopeptide antibiotic vancomycin. Evidence for an asparagine residue in the peptideJournal of the American Chemical Society, 1982
- Antibody affinity—III the role of multivalenceImmunochemistry, 1972