Two-Step Co-Immunoprecipitation (TIP)

Ruggero De Maria Marchiano, Tobias Longin Haas, Maria Rita Sciuto, Valeria Coppola, Gioacchin Iannolo

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

In the past few decades, numerous approaches have been developed to investigate protein-protein and protein-nucleic acid interactions (PPIs and PNIs). Affinity purification methods such as co-immunoprecipitation (co- IP) are commonly used to detect and isolate the macromolecular complexes resulting from these interactions. In this article, we describe a two-step coimmunoprecipitation (TIP) technique. As compared to standard co-IP, TIP provides increased specificity in the isolation of PPIs or PNIs under native expression conditions, dramatically reducing the abundance of nonspecific binders and thus facilitating downstream analyses of the interaction complexes. Here, we report a detailed TIP procedure that we used to purify a protein-protein complex from Burkitt lymphoma cells and from primary human CD4+ T cells. In addition, this unit describes an application of TIP for the isolation of transcription-factor-bound chromatin.
Original languageEnglish
Pages (from-to)e80-e100
Number of pages20
JournalCurrent Protocols in Molecular Biology
Volume125
DOIs
Publication statusPublished - 2019

Keywords

  • antibody
  • co-immunoprecipitation
  • protein-nucleic acid interaction
  • protein-protein interaction

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