Literature DB >> 10373602

A novel in vivo assay for the analysis of protein-protein interaction.

M Maroun1, A Aronheim.   

Abstract

The Ras Recruitment System (RRS) is a method for identification and isolation of protein-protein interaction. The method is based on translocation of cytoplasmic mammalian Ras protein to the inner leaflet of the plasma membrane through protein-protein interaction. The system is studied in a temperature-sensitive yeast strain where the yeast Ras guanyl nucleotide exchange factor is inactive at 36 degrees C. Protein-protein interaction results in cell growth at the restrictive temperature. We developed a gene reporter assay for the analysis of protein-protein interaction in mammalian cells. Ras activation in mammalian cells induces the mitogen-activated kinase cascade (MAPK), which can be monitored using Ras-dependent reporter genes. This greatly extends the usefulness of the system and provides a novel assay for protein-protein interaction in mammalian cells.

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Year:  1999        PMID: 10373602      PMCID: PMC148462          DOI: 10.1093/nar/27.13.e4

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  2 in total

Review 1.  Diversity in genetic in vivo methods for protein-protein interaction studies: from the yeast two-hybrid system to the mammalian split-luciferase system.

Authors:  Bram Stynen; Hélène Tournu; Jan Tavernier; Patrick Van Dijck
Journal:  Microbiol Mol Biol Rev       Date:  2012-06       Impact factor: 11.056

2.  Towards the systematic mapping and engineering of the protein prenylation machinery in Saccharomyces cerevisiae.

Authors:  Viktor Stein; Marta H Kubala; Jason Steen; Sean M Grimmond; Kirill Alexandrov
Journal:  PLoS One       Date:  2015-03-13       Impact factor: 3.240

  2 in total

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