A quantitative mass spectrometry-based approach to monitor the dynamics of endogenous chromatin-associated protein complexes

EK Papachristou, K Kishore, AN Holding, K Harvey, TI Roumeliotis, CSR Chilamakuri, S Omarjee, KM Chia, A Swarbrick, E Lim, F Markowetz, M Eldridge, R Siersbaek, CS D'Santos, JS Carroll

Research output: Contribution to journalArticlepeer-review


Understanding the dynamics of endogenous protein-protein interactions in complex networks is pivotal in deciphering disease mechanisms. To enable the in-depth analysis of protein interactions in chromatin-associated protein complexes, we have previously developed a method termed RIME (Rapid Immunoprecipitation Mass spectrometry of Endogenous proteins). Here, we present a quantitative multiplexed method (qPLEX-RIME), which integrates RIME with isobaric labelling and tribrid mass spectrometry for the study of protein interactome dynamics in a quantitative fashion with increased sensitivity. Using the qPLEX-RIME method, we delineate the temporal changes of the Estrogen Receptor alpha (ERα) interactome in breast cancer cells treated with 4-hydroxytamoxifen. Furthermore, we identify endogenous ERα-associated proteins in human Patient-Derived Xenograft tumours and in primary human breast cancer clinical tissue. Our results demonstrate that the combination of RIME with isobaric labelling offers a powerful tool for the in-depth and quantitative characterisation of protein interactome dynamics, which is applicable to clinical samples.
Original languageEnglish
Article number2311
Number of pages13
JournalNature Communications
Publication statusPublished - 13 Jun 2018

Bibliographical note

© 2018, The Author(s).

Cite this