Literature DB >> 20546956

Identifying components of protein complexes in C. elegans using co-immunoprecipitation and mass spectrometry.

James J Moresco1, Paulo C Carvalho, John R Yates.   

Abstract

Mass spectrometry-based proteomics is rapidly becoming an essential tool for biologists. One of the most common applications is identifying the components of protein complexes isolated by co-immunoprecipitation. In this review, we discuss the co-immunoprecipitation, mass spectrometry and data analysis techniques that have been used successfully to define protein complexes in C. elegans research. In this discussion, two strategies emerged. One approach is to use stringent biochemical purification methods and attempt to identify a small number of complex components with a high degree of certainty based on MS data. A second approach is to use less stringent purification and identification parameters, and ultimately test a longer list of potential binding partners in biological validation assays. This should provide a useful guide for biologists planning proteomic experiments.
Copyright © 2010 Elsevier B.V. All rights reserved.

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Year:  2010        PMID: 20546956      PMCID: PMC3279190          DOI: 10.1016/j.jprot.2010.05.008

Source DB:  PubMed          Journal:  J Proteomics        ISSN: 1874-3919            Impact factor:   4.044


  30 in total

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4.  Functional proteomics reveals the biochemical niche of C. elegans DCR-1 in multiple small-RNA-mediated pathways.

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Journal:  Cell       Date:  2006-01-27       Impact factor: 41.582

5.  Analysis of quantitative proteomic data generated via multidimensional protein identification technology.

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6.  Large-scale identification of Caenorhabditis elegans proteins by multidimensional liquid chromatography-tandem mass spectrometry.

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  13 in total

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2.  Cooperative transcription factor associations discovered using regulatory variation.

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Journal:  Proc Natl Acad Sci U S A       Date:  2011-07-26       Impact factor: 11.205

3.  Stable isotope labeling with amino acids in cell culture based mass spectrometry approach to detect transient protein interactions using substrate trapping.

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Review 5.  Worming our way in and out of the Caenorhabditis elegans germline and developing embryo.

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Journal:  Front Microbiol       Date:  2012-11-16       Impact factor: 5.640

Review 7.  Next-generation technologies for multiomics approaches including interactome sequencing.

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8.  Effective identification of Akt interacting proteins by two-step chemical crosslinking, co-immunoprecipitation and mass spectrometry.

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Review 9.  Protein-protein interaction detection: methods and analysis.

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10.  A tissue-specific protein purification approach in Caenorhabditis elegans identifies novel interaction partners of DLG-1/Discs large.

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Journal:  BMC Biol       Date:  2016-08-09       Impact factor: 7.431

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