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Design and nuclear magnetic resonance (NMR) structure determination of the second extracellular immunoglobulin tyrosine kinase A (TrkAIg2) domain construct for binding site elucidation in drug discovery

Research output: Contribution to journalArticle

Original languageEnglish
Pages (from-to)767-777
Number of pages11
JournalJournal of Medicinal Chemistry
Issue number2
Early online date2 Dec 2014
DateAccepted/In press - 27 Aug 2014
DateE-pub ahead of print - 2 Dec 2014
DatePublished (current) - 22 Jan 2015


The tyrosine kinase A (TrkA) receptor is a validated therapeutic intervention point for a wide range of conditions. TrkA activation by nerve growth factor (NGF) binding the second extracellular immunoglobulin (TrkAIg2) domain, triggers intracellular signalling cascades. In the periphery this promotes the pain phenotype and in the brain, cell survival or differentiation.
Reproducible structural information and detailed validation of protein-ligand interactions aid drug discovery. However, the isolated TrkAIg2 domain crystallizes as a β-strand-swapped dimer in the absence of NGF, occluding the binding surface. Here we report the design and structural validation by nuclear magnetic resonance spectroscopy of the first stable, biologically active construct of the TrkAIg2 domain for binding-site confirmation. Our structure closely mimics the wild-type fold of TrkAIg2 in complex with NGF (1WWW.pdb)
and the 1H-15N correlation spectra confirm that both NGF and a competing small molecule, interact at the known binding interface in solution.

    Research areas

  • TrkA, TrkAIg2, drug discovery, NMR construct, pain, Alzheimer’s

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