Allostery mediates ligand binding to WWOX tumor suppressor via a conformational switch

Brett J. Schuchardt, David C. Mikles, Vikas Bhat, Caleb B. McDonald, Marius Sudol, Amjad Farooq

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

While being devoid of the ability to recognize ligands itself, the WW2 domain is believed to aid ligand binding to the WW1 domain in the context of a WW1-WW2 tandem module of WW domain-containing oxidoreductase (WWOX) tumor suppressor. In an effort to test the generality of this hypothesis, we have undertaken here a detailed biophysical analysis of the binding of WW domains of WWOX alone and in the context of the WW1-WW2 tandem module to an array of putative proline-proline-x-tyrosine (PPXY) ligands. Our data show that while the WW1 domain of WWOX binds to all ligands in a physiologically relevant manner, the WW2 domain does not. Moreover, ligand binding to the WW1 domain in the context of the WW1-WW2 tandem module is two-to-three-fold stronger than when treated alone. We also provide evidence that the WW domains within the WW1-WW2 tandem module physically associate so as to adopt a fixed spatial orientation relative to each other. Of particular note is the observation that the physical association of the WW2 domain with WW1 blocks access to ligands. Consequently, ligand binding to the WW1 domain not only results in the displacement of the WW2 lid but also disrupts the physical association of WW domains in the liganded conformation. Taken together, our study underscores a key role of allosteric communication in the ability of the WW2 orphan domain to chaperone physiological action of the WW1 domain within the context of the WW1-WW2 tandem module of WWOX.

Original languageEnglish (US)
Pages (from-to)220-231
Number of pages12
JournalJournal of Molecular Recognition
Volume28
Issue number4
DOIs
StatePublished - 2015

Fingerprint

Ligands
Neoplasms
Proline
Tyrosine
Oxidoreductases

Keywords

  • allosteric communication
  • binding-coupled dissociation
  • equilibrium shift
  • WW tandem module
  • WW-ligand thermodynamics

ASJC Scopus subject areas

  • Molecular Biology
  • Structural Biology

Cite this

Allostery mediates ligand binding to WWOX tumor suppressor via a conformational switch. / Schuchardt, Brett J.; Mikles, David C.; Bhat, Vikas; McDonald, Caleb B.; Sudol, Marius; Farooq, Amjad.

In: Journal of Molecular Recognition, Vol. 28, No. 4, 2015, p. 220-231.

Research output: Contribution to journalArticle

Schuchardt, Brett J. ; Mikles, David C. ; Bhat, Vikas ; McDonald, Caleb B. ; Sudol, Marius ; Farooq, Amjad. / Allostery mediates ligand binding to WWOX tumor suppressor via a conformational switch. In: Journal of Molecular Recognition. 2015 ; Vol. 28, No. 4. pp. 220-231.
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