Defining the budding yeast chromatin-associated interactome

作者：Lambert Jean Philippe; Fillingham Jeffrey; Siahbazi Mojgan; Greenblatt Jack; Baetz Kristin; Figeys Daniel^*

来源：Molecular Systems Biology, 2010, 6(1): 448.

DOI：10.1038/msb.2010.104

• affinity purification
• chromatin-associated protein networks
• mass spectrometry
• nucleosome assembly factor Asf1
• protein-DNA interaction

We previously reported a novel affinity purification (AP) method termed modified chromatin immunopurification (mChIP), which permits selective enrichment of DNA- bound proteins along with their associated protein network. In this study, we report a large-scale study of the protein network of 102 chromatin-related proteins from budding yeast that were analyzed by mChIP coupled to mass spectrometry. This effort resulted in the detection of 2966 high confidence protein associations with 724 distinct preys. mChIP resulted in significantly improved interaction coverage as compared with classical AP methodology for similar to 75% of the baits tested. Furthermore, mChIP successfully identified novel binding partners for many lower abundance transcription factors that previously failed using conventional AP methodologies. mChIP was also used to perform targeted studies, particularly of Asf1 and its associated proteins, to allow for a understanding of the physical interplay between Asf1 and two other histone chaperones, Rtt106 and the HIR complex, to be gained. Molecular Systems Biology 6: 448; published online 21 December 2010; doi:10.1038/msb.2010.104

• 出版日期2010-12