Proximity-Dependent Biotinylation to Elucidate the Interactome of TNK2 Nonreceptor Tyrosine Kinase

Raiha Tahir, Anil K. Madugundu, Savita Udainiya, Jevon A. Cutler, Santosh Renuse, Li Wang, Nicole A. Pearson, Christopher J. Mitchell, Nupam Mahajan, Akhilesh Pandey, Xinyan Wu

Research output: Contribution to journalArticlepeer-review

Abstract

Nonreceptor tyrosine kinases (NRTKs) represent an important class of signaling molecules driving diverse cellular pathways. Aberrant expression and hyperphosphorylation of TNK2, an NRTK, have been implicated in multiple cancers. However, the exact proteins and cellular events that mediate phenotypic changes downstream of TNK2 are unclear. Biological systems that employ proximity-dependent biotinylation methods, such as BioID, are being increasingly used to map protein-protein interactions, as they provide increased sensitivity in discovering interaction partners. In this study, we employed stable isotope labeling with amino acids in cell culture and BioID coupled to the biotinylation site identification technology (BioSITe) method that we recently developed to quantitatively explore the interactome of TNK2. By performing a controlled comparative analysis between full-length TNK2 and its truncated counterpart, we were able to not only identify site-level biotinylation of previously well-established TNK2 binders and substrates including NCK1, NCK2, CTTN, and STAT3, but also discover several novel TNK2 interacting partners. We also performed co-immunoprecipitation and immunofluorescence analysis to validate the interaction between TNK2 and CLINT1, a novel TNK2 interacting protein. Overall, this work reveals the power of the BioSITe method coupled to BioID and highlights several molecules that warrant further exploration to assess their functional significance in TNK2-mediated signaling.

Original languageEnglish
Pages (from-to)4566-4577
Number of pages12
JournalJournal of Proteome Research
Volume20
Issue number9
DOIs
StatePublished - Sep 3 2021

Keywords

  • BioID
  • BioSITe
  • CLINT1
  • SILAC
  • TNK2
  • breast cancer
  • interactome
  • mass spectrometry
  • protein-protein interaction
  • proteomics

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