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An engineered Axl 'decoy receptor' effectively silences the Gas6-Axl signaling axis.

Abstract
Aberrant signaling through the Axl receptor tyrosine kinase has been associated with a myriad of human diseases, most notably metastatic cancer, identifying Axl and its ligand Gas6 as important therapeutic targets. Using rational and combinatorial approaches, we engineered an Axl 'decoy receptor' that binds Gas6 with high affinity and inhibits its function, offering an alternative approach from drug discovery efforts that directly target Axl. Four mutations within this high-affinity Axl variant caused structural alterations in side chains across the Gas6-Axl binding interface, stabilizing a conformational change on Gas6. When reformatted as an Fc fusion, the engineered decoy receptor bound Gas6 with femtomolar affinity, an 80-fold improvement compared to binding of the wild-type Axl receptor, allowing effective sequestration of Gas6 and specific abrogation of Axl signaling. Moreover, increased Gas6 binding affinity was critical and correlative with the ability of decoy receptors to potently inhibit metastasis and disease progression in vivo.
AuthorsMihalis S Kariolis, Yu Rebecca Miao, Douglas S Jones 2nd, Shiven Kapur, Irimpan I Mathews, Amato J Giaccia, Jennifer R Cochran
JournalNature chemical biology (Nat Chem Biol) Vol. 10 Issue 11 Pg. 977-83 (Nov 2014) ISSN: 1552-4469 [Electronic] United States
PMID25242553 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S.)
Chemical References
  • Immunoglobulin Fc Fragments
  • Intercellular Signaling Peptides and Proteins
  • Proto-Oncogene Proteins
  • Recombinant Fusion Proteins
  • growth arrest-specific protein 6
  • Receptor Protein-Tyrosine Kinases
  • Axl Receptor Tyrosine Kinase
Topics
  • Animals
  • Binding Sites
  • Disease Progression
  • Dose-Response Relationship, Drug
  • Genetic Engineering
  • Humans
  • Immunoglobulin Fc Fragments (chemistry, isolation & purification, pharmacology, therapeutic use)
  • Intercellular Signaling Peptides and Proteins (chemistry, metabolism)
  • Mice
  • Models, Molecular
  • Mutation (genetics)
  • Neoplasm Metastasis (drug therapy)
  • Neoplasms, Experimental (drug therapy, pathology)
  • Protein Binding (drug effects, genetics)
  • Proto-Oncogene Proteins (genetics, metabolism, pharmacology)
  • Receptor Protein-Tyrosine Kinases (genetics, metabolism, pharmacology)
  • Recombinant Fusion Proteins (chemistry, isolation & purification, metabolism, pharmacology)
  • Signal Transduction (drug effects)
  • Structure-Activity Relationship
  • Axl Receptor Tyrosine Kinase

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