| Literature DB >> 24658140 |
Julia Petschnigg1, Bella Groisman1, Max Kotlyar2, Mikko Taipale3, Yong Zheng4, Christoph F Kurat5, Azin Sayad1, J Rafael Sierra2, Mojca Mattiazzi Usaj1, Jamie Snider1, Alex Nachman1, Irina Krykbaeva3, Ming-Sound Tsao6, Jason Moffat7, Tony Pawson8, Susan Lindquist9, Igor Jurisica10, Igor Stagljar11.
Abstract
Cell signaling, one of key processes in both normal cellular function and disease, is coordinated by numerous interactions between membrane proteins that change in response to stimuli. We present a split ubiquitin-based method for detection of integral membrane protein-protein interactions (PPIs) in human cells, termed mammalian-membrane two-hybrid assay (MaMTH). We show that this technology detects stimulus (hormone or agonist)-dependent and phosphorylation-dependent PPIs. MaMTH can detect changes in PPIs conferred by mutations such as those in oncogenic ErbB receptor variants or by treatment with drugs such as the tyrosine kinase inhibitor erlotinib. Using MaMTH as a screening assay, we identified CRKII as an interactor of oncogenic EGFR(L858R) and showed that CRKII promotes persistent activation of aberrant signaling in non-small cell lung cancer cells. MaMTH is a powerful tool for investigating the dynamic interactomes of human integral membrane proteins.Entities:
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Year: 2014 PMID: 24658140 DOI: 10.1038/nmeth.2895
Source DB: PubMed Journal: Nat Methods ISSN: 1548-7091 Impact factor: 28.547