A Differential Cytolocalization Assay for Analysis of Macromolecular Assemblies in the Eukaryotic Cytoplasm
We have developed a differential cytolocalization assay (DCLA) that allows the observation of cytoplasmic protein/protein interactions in vivo . In the DCLA, interactions are visualized as a relocalization of a green fluorescent protein-tagged âpreyâ by a membrane-bound âbait.â This assay wa...
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Published in | Molecular & cellular proteomics Vol. 5; no. 11; pp. 2175 - 2184 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
United States
American Society for Biochemistry and Molecular Biology
01.11.2006
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Subjects | |
Online Access | Get full text |
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Summary: | We have developed a differential cytolocalization assay (DCLA) that allows the observation of cytoplasmic protein/protein
interactions in vivo . In the DCLA, interactions are visualized as a relocalization of a green fluorescent protein-tagged âpreyâ by a membrane-bound
âbait.â This assay was tested and utilized in Caenorhabditis elegans to probe interactions among proteins involved in RNA interference (RNAi) and nonsense-mediated decay (NMD) pathways. Several
previously documented interactions were confirmed with DCLA, whereas uniformly negative results were obtained in several controls
in which no interaction was expected. Novel interactions were also observed, including the association of SMG-5, a protein
required for NMD, to several components of the RNAi pathway. The DCLA can be readily carried out under diverse conditions,
allowing a dynamic assessment of protein interactions in vivo . We used this property to test a subset of the RNAi and NMD interactions in animals in which proteins central to each mechanism
were mutated; several key associations in each machinery that can occur in vivo in the absence of a functional process were identified. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1535-9476 1535-9484 |
DOI: | 10.1074/mcp.T600025-MCP200 |