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Science 1 May 1998: Vol. 280. no. 5364, pp. 708 - 711 DOI: 10.1126/science.280.5364.708
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Reports
A Trivalent System from Vancomycin·D-Ala-D-Ala with Higher Affinity Than Avidin·Biotin
Jianghong Rao,
Joydeep Lahiri,
Lyle Isaacs,
Robert M. Weis,
George M. Whitesides
*
Tris(vancomycin carboxamide) binds a trivalent ligand derived from
D-Ala-D-Ala with very high affinity:
dissociation constant (Kd) 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.
J. Rao, J. Lahiri, L. Isaacs, G. M. Whitesides, Department of
Chemistry and Chemical Biology, Harvard University, 12 Oxford Street,
Cambridge, MA 02138, USA.
R. M. Weis, Department of Chemistry, University of Massachusetts,
Amherst, MA 01003, USA.
*
To whom correspondence should be addressed. E-mail:
gwhitesides{at}gmwgroup.harvard.edu
Read the Full Text
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