In vivo supramolecular templating enhances the activity of multivalent ligands: A potential therapeutic against the Escherichia coli O157 AB^sub 5^ toxins

We demonstrate that interactions between multimeric receptors and multivalent ligands are dramatically enhanced by recruiting a complementary templating receptor such as an endogenous multimeric protein but only when individual ligands are attached to a polymer as preorganized, covalent, heterobifun...

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Bibliographic Details
Published in:Proceedings of the National Academy of Sciences - PNAS 2008-11, Vol.105 (44), p.16837
Main Authors: Kitov, Pavel I, Mulvey, George L, Griener, Thomas P, Lipinski, Tomasz, Solomon, Dmitry, Paszkiewicz, Eugenia, Jacobson, Jared M, Sadowska, Joanna M, Suzuki, Missao, Yamamura, Ken-ichi, Armstrong, Glen D, Bundle, David R
Format: Article
Language:English
Subjects:
Biochemistry
E coli
Molecular biology
Molecules
Proteins
Toxins
Online Access:Get full text
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Summary:We demonstrate that interactions between multimeric receptors and multivalent ligands are dramatically enhanced by recruiting a complementary templating receptor such as an endogenous multimeric protein but only when individual ligands are attached to a polymer as preorganized, covalent, heterobifunctional pairs. This effect cannot be replicated by a multivalent ligand if the same recognition elements are independently arrayed on the scaffold. Application of this principle offers an approach to create high-avidity inhibitors for multimeric receptors. Judicious selection of the ligand that engages the templating protein allows appropriate effector function to be incorporated in the polymeric construct, thereby providing an opportunity for therapeutic applications. The power of this approach is exemplified by the design of exceptionally potent Escherichia coli Shiga toxin antagonists that protect transgenic mice that constitutively express a human pentraxin, serum amyloid P component. [PUBLICATION ABSTRACT]
ISSN:0027-8424
1091-6490