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Adenosine deaminase is a specific partner for the Grb2 isoform Grb3-3.
- Source :
-
Biochemical and biophysical research communications [Biochem Biophys Res Commun] 1997 Aug 28; Vol. 237 (3), pp. 735-40. - Publication Year :
- 1997
-
Abstract
- Grb3-3 is an isoform of Grb2, thought to arise by alternative splicing, that lacks a functional SH2 domain but retains functional SH3 domains, which allow interaction with other proteins through binding to prolinerich sequences. Several evidences suggest that besides common partners for Grb2 and Grb3-3, specific targets could exist. In order to find specific partners for Grb3-3, we have screened a human cDNA library by the yeast two-hybrid system with Grb3-3 as a bait. We have identified adenosine deaminase, an enzyme involved in purine metabolism whose deficiency is associated with severe combined immunodeficiency, as a Grb3-3 binding protein that is not able to bind to Grb2. This interaction has been confirmed in vitro with GST fusion proteins and in vivo by coimmunoprecipitation experiments in NIH3T3 cells stably transfected with Grb3-3. The functional significance of this finding is discussed.
- Subjects :
- 3T3 Cells
Adenosine Deaminase biosynthesis
Adenosine Deaminase isolation & purification
Animals
Cloning, Molecular
DNA, Complementary
ErbB Receptors metabolism
GRB2 Adaptor Protein
Gene Library
Glutathione Transferase
HeLa Cells
Humans
Jurkat Cells
Mice
Polymerase Chain Reaction
Protein Biosynthesis
Proteins isolation & purification
Recombinant Fusion Proteins metabolism
Recombinant Proteins biosynthesis
Recombinant Proteins isolation & purification
Recombinant Proteins metabolism
Saccharomyces cerevisiae
Transfection
src Homology Domains
Adaptor Proteins, Signal Transducing
Adenosine Deaminase metabolism
Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0006-291X
- Volume :
- 237
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Biochemical and biophysical research communications
- Publication Type :
- Academic Journal
- Accession number :
- 9299436
- Full Text :
- https://doi.org/10.1006/bbrc.1997.7221