In situ assay of light-stimulated G protein activity in Drosophila photoreceptor G protein beta mutants.

نویسندگان

  • S L Yarfitz
  • J L Running Deer
  • G Froelick
  • N J Colley
  • J B Hurley
چکیده

An in situ 35S-labeled guanosine 5'-3-O-(thio)triphosphate (GTP gamma S) binding procedure was developed to assay light-stimulated G protein activity in Drosophila compound eyes. We found that Drosophila with mutations in G beta e, an abundant photoreceptor-specific G protein beta subunit essential for photoexcitation, are defective in light-stimulated [35S]GTP gamma S binding. We confirmed that G beta e interacts with a GTP-binding protein by demonstrating that immunoprecipitation of G beta e is sensitive to GTP gamma S. These results suggest that G beta e functions as the beta subunit of a heterotrimeric G protein that couples photoactivation of rhodopsin to downstream components in the Drosophila phototransduction cascade.

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عنوان ژورنال:
  • The Journal of biological chemistry

دوره 269 48  شماره 

صفحات  -

تاریخ انتشار 1994