2ER membrane and lumenal protein interaction yeast two-hybrid assay
AssigneeNational Research Council of Canada
InventorsMarc F. Pelletier, Gregor Jansen, John J.M. Bergeron, David Y. Thomas
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AssigneeNational Research Council of Canada
InventorsMarc F. Pelletier, Gregor Jansen, John J.M. Bergeron, David Y. Thomas
Estimating the term…
The present invention relates to a new yeast two-hybrid system for the detection of interactions between membrane proteins and lumenal proteins of the endoplasmic reticulum. The yeast two-hybrid system of the present invention uses the IRE1 gene of yeast which is a key element in the endoplasmic reticulum unfolded protein response to signal the interaction between proteins within the endoplasmic reticulum. The IRE1 gene codes for a type 1 membrane protein Ire1p, that has a kinase in the cytosolic domain and it signals the presence of unfolded proteins in the ER by oligomerization and transphosphorylation, this in turn activates a RNaseL that has as its unique (so far) substrate the HAC1 messenger RNA, that codes for the transcription factor that binds to the unfolded protein response element and upregulates transcription of ER protein required for folding proteins within the ER. The yeast two-hybrid system of the present invention uses in-reading frame fusions of ER proteins to the N-terminal “protein sensing domain” of Ire1p to detect their interaction using Ire1p dimerization and the unfolded protein response system as a read out. This readout is made simpler by the use of reporter gene systems making the system suitable for mass screening of ER protein interactions.
A yeast two-hybrid assay for detection of interactions between at least two endoplasmic reticulum membrane and/or lumenal proteins of interest capable of or suspected of interacting, which comprises:
The method of claim 12, wherein regions of protein-protein interaction of calnexin and calreticulin with Erp57 is mapped.
Dependencies are inferred from the claim text.