{"doi":"10.1101/pdb.prot5605","title":"Making Yeast Cell Extracts for Purifying TAP-tagged Protein Complexes","abstract":"<jats:title>INTRODUCTION</jats:title><jats:p>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. The 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 extract from TAP-tagged yeast cells for use in purifying TAP-tagged protein complexes.</jats:p>","journal":"Cold Spring Harbor Protocols","year":2011,"id":40648,"datarank":0.20794415416798362,"base_score":1.3862943611198906,"endowment":1.3862943611198906,"self_citation_contribution":0.20794415416798362,"citation_network_contribution":0.0,"self_endowment_contribution":0.20794415416798362,"citer_contribution":0.0,"corpus_percentile":null,"corpus_rank":null,"citation_count":3,"citer_count":0,"citers_with_citation_signal":0,"citers_with_endowment":0,"datacite_reuse_total":0,"is_dataset":false,"is_dataset_confidence":null,"is_data_producer":false,"deposit_databanks":null,"is_oa":false,"file_count":0,"downloads":0,"has_version_chain":false,"published_date":null,"fair_score":null,"fair_percentile":null,"algorithm_id":"datarank_citation_only_1hop_v6","ranking_scope":"data_only","authors":[{"id":197113,"name":"Connie Weaver","orcid":null,"position":1,"is_corresponding":false},{"id":197114,"name":"Adam Farley","orcid":null,"position":2,"is_corresponding":false},{"id":197112,"name":"Andrew J. Link","orcid":null,"position":0,"is_corresponding":false}],"reference_count":0,"raw_metadata":{"has_enrichment":true,"base_score":0.0,"endowment":0.0,"datacite_reuse_total":0,"file_count":0,"downloads":0,"views":0,"has_version_chain":false,"is_dataset":false,"is_oa":false,"pmid":"21460054","pmcid":null,"openalex_id":"https://openalex.org/W21460054","authors":[],"funders":[],"total_grants":0,"fwci":null,"citation_percentile":null,"influential_citations":0,"citation_trend":[],"oa_status":"closed","license":null,"oa_locations":[{"url":"https://syndication.highwire.org/content/doi/10.1101/pdb.prot5605","host_type":"publisher"},{"url":"https://ci.nii.ac.jp/naid/110007485434","host_type":"journal"}],"fields_of_study":["Military Technology and Strategies","Legal and Regulatory Analysis","Linguistic, Cultural, and Literary Studies","Chemistry","Medicine","Biology","Chromatography, Affinity","Complex Mixtures","Fungal Proteins","Protein Interaction Mapping","Recombinant Fusion Proteins","Yeasts"],"mesh_terms":["Yeasts","Fungal Proteins","Recombinant Fusion Proteins","Complex Mixtures","Chromatography, Affinity","Protein Interaction Mapping"],"keywords":["High-performance liquid chromatography","Chemistry","Chromatography","Computer science"],"sdg_mappings":[],"linked_datasets":[],"clinical_trials":[],"software_tools":[],"database_accessions":[],"source":"live","citation_network_status":"fetched"},"created_at":"2026-06-12T08:45:55.845017Z","pmid":null,"pmcid":null,"fwci":null,"citation_percentile":null,"influential_citations":0,"oa_status":null,"license":null,"views":0,"total_file_size_bytes":0,"version_count":0,"fair_f":null,"fair_a":null,"fair_i":null,"fair_r":null,"fair_zscore":null,"fair_rationale":null,"fair_model":null,"fair_agent_version":null,"fair_fulltext_source":null,"fair_has_llm":null,"fair_computed_at":null,"clinical_trials":[],"software_tools":[],"db_accessions":[],"linked_datasets":[],"topics":[]}