Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1991 Oct 1;279 ( Pt 1)(Pt 1):43-8.
doi: 10.1042/bj2790043.

Redistribution of 23 kDa tubulovesicle-associated GTP-binding proteins during parietal cell stimulation

Affiliations

Redistribution of 23 kDa tubulovesicle-associated GTP-binding proteins during parietal cell stimulation

M D Basson et al. Biochem J. .

Abstract

Small GTP-binding proteins are important regulators of intracellular traffic. The presence of several small GTP-binding proteins was documented in subfractions of rabbit parietal cells. Upon maximal stimulation of the cells with a combination of histamine and forskolin, one 23 kDa GTP-binding band was observed to decrease in a 50,000 g membrane fraction while increasing in 4000 g membranes. The 23 kDa band resolved into one major and two minor species on two-dimensional gels. GTP-binding species of 23 kDa, 24 kDa and 25 kDa were present in purified preparations of tubulovesicles. The three isoelectric species of the 23 kDa proteins observed in parietal cell 50,000 g microsomes were enriched in tubulovesicle preparations. None of the tubulovesicle-associated GTP-binding proteins were substrates for ADP-ribosylation by a preparation of botulinum D toxin. These results indicate that tubulovesicles contain discrete small GTP-binding proteins which redistribute during parietal cell stimulation.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Biochem J. 1989 Sep 1;262(2):497-503 - PubMed
    1. J Biol Chem. 1989 Nov 5;264(31):18363-7 - PubMed
    1. J Biol Chem. 1988 Nov 15;263(32):16744-9 - PubMed
    1. J Biol Chem. 1988 Nov 5;263(31):16303-8 - PubMed
    1. Trends Pharmacol Sci. 1989 Oct;10(10):415-8 - PubMed

Publication types

MeSH terms