A mass spectrometry view of stable and transient protein interactions

Hanna G. Budayeva, Ileana M. Cristea

Research output: Contribution to journalArticle

16 Scopus citations

Abstract

Through an impressive range of dynamic interactions, proteins succeed to carry out the majority of functions in a cell. These temporally and spatially regulated interactions provide the means through which one single protein can perform diverse functions and modulate different cellular pathways. Understanding the identity and nature of these interactions is therefore critical for defi ning protein functions and their contribution to health and disease processes. Here, we provide an overview of workfl ows that incorporate immunoaffi nity purifi cations and quantitative mass spectrometry (frequently abbreviated as IP-MS or AP-MS) for characterizing protein–protein interactions. We discuss experimental aspects that should be considered when optimizing the isolation of a protein complex. As the presence of nonspecifi c associations is a concern in these experiments, we discuss the common sources of nonspecifi c interactions and present label-free and metabolic labeling mass spectrometry-based methods that can help determine the specifi city of interactions. The effective regulation of cellular pathways and the rapid reaction to various environmental stresses rely on the formation of stable, transient, and fast-exchanging protein–protein interactions. While determining the exact nature of an interaction remains challenging, we review cross-linking and metabolic labeling approaches that can help address this important aspect of characterizing protein interactions and macromolecular assemblies.

Original languageEnglish (US)
Pages (from-to)263-282
Number of pages20
JournalAdvances in experimental medicine and biology
Volume806
DOIs
StatePublished - 2014

All Science Journal Classification (ASJC) codes

  • Biochemistry, Genetics and Molecular Biology(all)

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