1. Academic Validation
  2. Selective, tight-binding inhibitors of integrin alpha4beta1 that inhibit allergic airway responses

Selective, tight-binding inhibitors of integrin alpha4beta1 that inhibit allergic airway responses

  • J Med Chem. 1999 Mar 11;42(5):920-34. doi: 10.1021/jm980673g.
K c Lin 1 H S Ateeq S H Hsiung L T Chong C N Zimmerman A Castro W C Lee C E Hammond S Kalkunte L L Chen R B Pepinsky D R Leone A G Sprague W M Abraham A Gill R R Lobb S P Adams
Affiliations

Affiliation

  • 1 Biogen Inc., 12 Cambridge Center, Cambridge, Massachusetts 02142, and Mount Sinai Medical Center, Miami Beach, Florida 33140, USA.
Abstract

Integrin alpha4beta1 mediates leukocyte recruitment, activation, mediator release, and Apoptosis inhibition, and it plays a central role in inflammatory pathophysiology. High-affinity, selective inhibitors of alpha4beta1, based on the Leu-Asp-Val (LDV) sequence from the alternatively spliced connecting segment-1 (CS-1) peptide of cellular fibronectin, are described that employ a novel N-terminal peptide "cap" strategy. One inhibitor, BIO-1211, was approximately 10(6)-fold more potent than the starting peptide and exhibited tight-binding properties (koff = 1.4 x 10(-4) s-1, KD = 70 pM), a remarkable finding for a noncovalent, small-molecule inhibitor of a protein receptor. BIO-1211 was also 200-fold selective for the activated form of alpha4beta1, and it stimulated expression of ligand-induced epitopes on the Integrin beta1 subunit, a property consistent with occupancy of the receptor's ligand-binding site. Pretreatment of allergic sheep with a 3-mg nebulized dose of BIO-1211 inhibited early and late airway responses following antigen challenge and prevented development of nonspecific airway hyperresponsiveness to carbachol. These results show that highly selective and potent small-molecule antagonists can be identified to integrins with primary specificity for peptide domains other than Arg-Gly-Asp (RGD); they confirm the generality of integrins as small molecule targets; and they validate alpha4beta1 as a therapeutic target for asthma.

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