Evidence map›Paper›PMID 18629296›Full record

ArticleComparative and functional genomics2005

Construction, verification and experimental use of two epitope-tagged collections of budding yeast strains.

Russell Howson, Won-Ki Huh, Sina Ghaemmaghami, James V Falvo, Kiowa Bower, Archana Belle, Noah Dephoure, Dennis D Wykoff, Jonathan S Weissman, Erin K O'Shea

Abstract read
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Article in Comparative and functional genomics, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

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0cells of the map it votes in
49citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

49 citing papers in PubMed.

  1. Med9 Is a Novel eIF4E-Interacting Protein inInternational journal of molecular sciences · 2026
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  4. Modular gene tagging inbioRxiv : the preprint server for biology · 2026
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  5. Review
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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Russell HowsonDepartment of Biochemistry and Biophysics, Howard Hughes Medical Institute, University of California at San Francisco, 600 16th Street, Genentech Hall, San Francisco, CA 94143-2240, USA.
Won-Ki Huh
Sina Ghaemmaghami
James V Falvo
Kiowa Bower
Archana Belle
Noah Dephoure
Dennis D Wykoff
Jonathan S Weissman
Erin K O'Shea

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A major challenge in the post-genomic era is the development of experimental approaches to monitor the properties of proteins on a proteome-wide level. It would be particularly useful to systematically assay protein subcellular localization, post-translational modifications and protein-protein interactions, both at steady state and in response to environmental stimuli. Development of new reagents and methods will enhance our ability to do so efficiently and systematically. Here we describe the construction of two collections of budding yeast strains that facilitate proteome-wide measurements of protein properties. These collections consist of strains with an epitope tag integrated at the C-terminus of essentially every open reading frame (ORF), one with the tandem affinity purification (TAP) tag, and one with the green fluorescent protein (GFP) tag. We show that in both of these collections we have accurately tagged a high proportion of all ORFs (approximately 75% of the proteome) by confirming expression of the fusion proteins. Furthermore, we demonstrate the use of the TAP collection in performing high-throughput immunoprecipitation experiments. Building on these collections and the methods described in this paper, we hope that the yeast community will expand both the quantity and type of proteome level data available.

Identifiers

PMID18629296
PMCPMC2448600

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.