Protocol

Growing and Harvesting TAP-Tagged Yeast Cells

Adapted from Proteomics: A Cold Spring Harbor Laboratory Course Manual (ed. Link and LaBaer). CSHL Press, Cold Spring Harbor, NY, USA, 2009.

INTRODUCTION

One approach to identifying protein–protein interactions is the biochemical purification of a target protein from cells or tissues under nondenaturing conditions followed by the mass spectrometric identification of the components of the purified protein complex. This combination of highly specific protein purification strategies and mass spectrometry has proven to be a very successful approach for identifying protein–protein interactions. The tandem affinity purification (TAP) affinity tag and purification method allows efficient recovery of proteins present at low cellular concentrations under native conditions. Expressing the target protein at its natural levels avoids the assembly of overexpressed proteins into nonphysiological complexes. This protocol describes the preparation of TAP-tagged yeast cells.

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