1. Academic Validation
  2. Two-Step Co-Immunoprecipitation (TIP)

Two-Step Co-Immunoprecipitation (TIP)

  • Curr Protoc Mol Biol. 2019 Jan;125(1):e80. doi: 10.1002/cpmb.80.
Maria Rita Sciuto 1 Valeria Coppola 1 Gioacchin Iannolo 2 Ruggero De Maria 3 4 Tobias L Haas 3 4
Affiliations

Affiliations

  • 1 Department of Oncology and Molecular Medicine, Istituto Superiore di Sanità, Rome, Italy.
  • 2 Regenerative Medicine and Biomedical Technologies Unit, Department of Laboratory Medicine and Advanced Biotechnologies, IRCCS-ISMETT, Palermo, Italy.
  • 3 Institute of General Pathology, Università Cattolica del Sacro Cuore, Rome, Italy.
  • 4 Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
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 complexesresulting from these interactions. In this article, we describe a two-step co-immunoprecipitation (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. © 2018 by John Wiley & Sons, Inc.

Keywords

antibody; co-immunoprecipitation; protein-nucleic acid interaction; protein-protein interaction.

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