Molecularly imprinted nanoparticles reveal regulatory scaffolding features in Pyk2 tyrosine kinase.
Tania M Palhano ZanelaMilad ZangiabadiYan ZhaoEric S UnderbakkePublished in: RSC chemical biology (2024)
Pyk2 is a multi-domain non-receptor tyrosine kinase that serves dual roles as a signaling enzyme and scaffold. Pyk2 activation involves a multi-stage cascade of conformational rearrangements and protein interactions initiated by autophosphorylation of a linker site. Linker phosphorylation recruits Src kinase, and Src-mediated phosphorylation of the Pyk2 activation loop confers full activation. The regulation and accessibility of the initial Pyk2 autophosphorylation site remains unclear. We employed peptide-binding molecularly imprinted nanoparticles (MINPs) to probe the regulatory conformations controlling Pyk2 activation. MINPs differentiating local structure and phosphorylation state revealed that the Pyk2 autophosphorylation site is protected in the autoinhibited state. Activity profiling of Pyk2 variants implicated FERM and linker residues responsible for constraining the autophosphorylation site. MINPs targeting each Src docking site disrupt the higher-order kinase interactions critical for activation complex maturation. Ultimately, MINPs targeting key regulatory motifs establish a useful toolkit for probing successive activational stages in the higher-order Pyk2 signaling complex.
Keyphrases
- tyrosine kinase
- molecularly imprinted
- epidermal growth factor receptor
- transcription factor
- molecular dynamics simulations
- protein kinase
- single cell
- solid phase extraction
- single molecule
- gene expression
- computed tomography
- magnetic resonance imaging
- magnetic resonance
- mass spectrometry
- liquid chromatography
- dna binding