PLoS ONE (Jan 2017)

ANKRD54 preferentially selects Bruton's Tyrosine Kinase (BTK) from a Human Src-Homology 3 (SH3) domain library.

  • Manuela O Gustafsson,
  • Dara K Mohammad,
  • Erkko Ylösmäki,
  • Hyunseok Choi,
  • Subhash Shrestha,
  • Qing Wang,
  • Beston F Nore,
  • Kalle Saksela,
  • C I Edvard Smith

DOI
https://doi.org/10.1371/journal.pone.0174909
Journal volume & issue
Vol. 12, no. 4
p. e0174909

Abstract

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Bruton's Tyrosine Kinase (BTK) is a cytoplasmic protein tyrosine kinase with a fundamental role in B-lymphocyte development and activation. The nucleocytoplasmic shuttling of BTK is specifically modulated by the Ankyrin Repeat Domain 54 (ANKRD54) protein and the interaction is known to be exclusively SH3-dependent. To identify the spectrum of the ANKRD54 SH3-interactome, we applied phage-display screening of a library containing all the 296 human SH3 domains. The BTK-SH3 domain was the prime interactor. Quantitative western blotting analysis demonstrated the accuracy of the screening procedure. Revealing the spectrum and specificity of ANKRD54-interactome is a critical step toward functional analysis in cells and tissues.