| Literature DB >> 27631806 |
Ivo A Hendriks1, Alfred C O Vertegaal2.
Abstract
Mass spectrometry-based approaches are utilized with increasing frequency to facilitate identification of novel SUMO target proteins and to elucidate the dynamics of SUMOylation in response to cellular stresses. Here, we describe a robust method for the identification of SUMO target proteins, and the relative quantification of SUMOylation dynamics, using a label-free approach. The method relies on a decahistidine (His10)-tagged SUMO, which is expressed at a low level in a mammalian cell line or model organism. The His10-tag allows for a single-step, high-yield, and high-purity enrichment of SUMOylated proteins, which are then digested and analyzed by high-resolution mass spectrometry. Matching between runs and label-free quantification integrated in the freely available MaxQuant software allow for a high rate and accuracy of quantification, providing a strong alternative to laborious sample or cell labeling techniques. The method described here allows for identification of >1000 SUMO target proteins, and characterization of their SUMOylation dynamics, without requiring sample fractionation. The purification procedure, starting from total lysate, can be performed in ~4 days.Entities:
Keywords: His10 pulldown; Label-free quantification; Mass spectrometry; Proteomics; SUMO; SUMO target purification
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Year: 2016 PMID: 27631806 DOI: 10.1007/978-1-4939-6358-4_13
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745