Tandem affinity purification (TAP) coupled to mass spectrometry has become a powerful approach to identify protein-protein interactions from different biological systems, including plants, in a proteome-wide manner. By using two sequential affinity purification steps, TAP allows for isolation of high-purity TAP-tagged proteins of interest and their associated proteins. Here we describe optimized procedures to use the GS TAP technology for protein complex isolation from Arabidopsis cell suspension cultures.
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http://dx.doi.org/10.1007/978-1-4939-7871-7_21 | DOI Listing |
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