Literature DB >> 1660147

A contingent replication assay for the detection of protein-protein interactions in animal cells.

H A Vasavada1, S Ganguly, F J Germino, Z X Wang, S M Weissman.   

Abstract

We have developed a sensitive and rapid assay system termed the contingent replication assay (CRA) for selecting cDNAs with desired functional properties from a cDNA library. The system functions in animal cells and permits enrichment of the desired cDNA in small-scale and convenient experiments. The assay can be used for the enrichment of proteins that activate transcription from conditional enhancers, bind to specific DNA sequences, or interact with target proteins of interest. In this communication we report the application of this assay to study protein-protein interactions in animal cells.

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Year:  1991        PMID: 1660147      PMCID: PMC52995          DOI: 10.1073/pnas.88.23.10686

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  26 in total

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4.  Contingent replication assay (CRA) procedure for rapid isolation of enhancers.

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5.  Resolution and partial characterization of factors required for in vitro transcription by mammalian RNA polymerase II.

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Journal:  Proc Natl Acad Sci U S A       Date:  1989-08       Impact factor: 11.205

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7.  Use of gene fusions and protein-protein interaction in the isolation of a biologically active regulatory protein: the replication initiator protein of plasmid R6K.

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9.  Factors involved in specific transcription by mammalian RNA polymerase II. Purification and functional analysis of general transcription factor IIE.

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9.  Evaluation of the contingent replication assay (CRA) and its application to the study of the general transcription initiation factor, TFIIF.

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10.  Domain structure of a human general transcription initiation factor, TFIIF.

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