293T cells were transferred with PLK2. Membrane-associated proteins were collected and isolated. The supernatants containing solubilized membrane and membrane-associated proteins were collected and incubated. Supernatants from both extraction steps were pooled and incubated with Dynabeads Protein A/G preconjugated with the appropriate antibody. IP products were reduced with 20 mM dithiothreitol, followed by alkylation. Proteins were digested with trypsin. Peptides were desalted using STAGE TIP before downstream mass spectrometry analysis. MS experiments were conducted using a nanoscale ultra-high-performance liquid chromatography system connected to an Orbitrap Q-Exactive mass spectrometer equipped with a nanoelectrospray source. Raw data were processed using Proteome Discoverer, and MS/MS spectra were searched against the reviewed Swiss-Prot human proteome database.