These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Search MEDLINE/PubMed

  • Title: G protein subtype specificity of rhodopsin intermediates metarhodopsin Ib and metarhodopsin II.
    Author: Morizumi T, Kimata N, Terakita A, Imamoto Y, Yamashita T, Shichida Y.
    Journal: Photochem Photobiol; 2009; 85(1):57-62. PubMed ID: 18643908.
    Abstract:
    Rhodopsin is one of the members of the G protein-coupled receptor family that can catalyze a GDP-GTP exchange reaction on the retinal G protein transducin (Gt) upon photon absorption. There are at least two intermediate states, meta-Ib and meta-II, which exhibit direct interaction with Gt. Meta-Ib binds to GDP-bound Gt, while meta-II forms a complex with Gt having no nucleotide, suggesting that meta-Ib is a state that initially interacts with Gt. Here we investigated whether or not meta-Ib exhibits specific interaction with G protein similar to meta-II, by examining the binding efficiencies of meta-Ib and meta-II to Gialpha and its mutants whose C-terminal 11 amino acids were replaced with those of Goalpha, Gqalpha and Gsalpha. The affinity of meta-Ib to the C-terminal 11 amino acids of Gtalpha was similar to those of Gialpha and its mutant with Goalpha's C-terminal 11 amino acids, whereas meta-II exhibited affinity to the C-terminal 11 amino acids of Gialpha mutant with Goalpha's C-terminal 11 amino acids about half of what was seen for Gtalpha and Gialpha. Both intermediates exhibited no affinity to the Gialpha mutants containing the C-terminal 11 amino acids of Gqalpha and Gsalpha. These results suggested that meta-Ib is the state that exhibits specific interaction with G protein as meta-II does, although meta-Ib exhibits a slightly lenient binding selectivity compared to that of meta-II.
    [Abstract] [Full Text] [Related] [New Search]