Literature DB >> 15644491

A combined approach for the localization and tandem affinity purification of protein complexes from metazoans.

Iain M Cheeseman1, Arshad Desai.   

Abstract

An understanding of a protein's function is greatly aided by the knowledge of its localization in vivo and identification of any interacting partners. Here, we describe a method, based on expression of a genetically encoded fusion protein, that allows for protein localization and affinity purification (LAP) in metazoans. This method makes it possible to rapidly identify transformants and to conduct live imaging of protein localization and dynamics. In addition, the same tag can be used in a modified tandem affinity purification (TAP) procedure to isolate native protein complexes of high purity. The efficacy of this purification procedure allows for the characterization of rare protein complexes that are largely inaccessible to classical biochemical purifications. The LAP strategy should be widely applicable to the characterization of protein function in cellular and developmental contexts in various metazoans.

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Year:  2005        PMID: 15644491     DOI: 10.1126/stke.2662005pl1

Source DB:  PubMed          Journal:  Sci STKE        ISSN: 1525-8882


  143 in total

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5.  The CENP-L-N Complex Forms a Critical Node in an Integrated Meshwork of Interactions at the Centromere-Kinetochore Interface.

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Journal:  Cell Cycle       Date:  2009-02-17       Impact factor: 4.534

9.  TD-60 is required for interphase cell cycle progression.

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10.  An Afg2/Spaf-related Cdc48-like AAA ATPase regulates the stability and activity of the C. elegans Aurora B kinase AIR-2.

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Journal:  Dev Cell       Date:  2008-10       Impact factor: 12.270

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