A cell-based protein-protein interaction method using a permuted luciferase reporter
We have developed a novel cell-based protein-protein interaction assay method. The method relies on conversion of an inactive permuted luciferase containing a Tobacco Etch Virus protease (TEV) cleavage sequence fused onto protein (A) to an active luciferase upon interaction and cleavage by another p...
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Published in: | Current chemical genomics Vol. 5; pp. 122 - 128 |
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Main Authors: | , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
United Arab Emirates
Bentham Open
2011
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Subjects: | |
Online Access: | Get full text |
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Summary: | We have developed a novel cell-based protein-protein interaction assay method. The method relies on conversion of an inactive permuted luciferase containing a Tobacco Etch Virus protease (TEV) cleavage sequence fused onto protein (A) to an active luciferase upon interaction and cleavage by another protein (B) fused with the TEV protease. We demonstrate assay applicability for ligand-induced protein-protein interactions including G-protein coupled receptors, receptor tyrosine kinases and nuclear hormone receptors. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1875-3973 1875-3973 |
DOI: | 10.2174/1875397301105010122 |