» Articles » PMID: 60760

Small Fragments from the A Subunit of Cholera Toxin Capable of Activating Adenylate Cyclase

Overview
Specialty Science
Date 1976 Aug 1
PMID 60760
Citations 7
Authors
Affiliations
Soon will be listed here.
Abstract

Exposure of cholera toxin to membrane particles prepared from sarcoma 180 cells gives rise to a variety of fragments which are capable of activating adenylate cyclase [ATP:pyrophosphate-lyase (cyclizing), EC 4.6.1.1]. A major component of these fragments has an apparent molecular weight in the 8,000-10,000 range. The smallest stimulatory fragment has a molecular weight of approximately 1400. The small size of the fragments is confirmed by Sephadex gel filtration, in the presence of either sodium dodecyl sulfate or formic acid. These fragments are produced from holotoxin or its A subunit by protease(s) found in sarcoma membrane particles. Production of fragments appears optimal in 40-60 min at 30 degrees and pH 7, and is prevented by protease inhibitors. The ability of the small fragments to activate adenylate cyclase is reversed by anti-holotoxin, but not anticholeragenoid, antibodies. These fragments require NAD for the activation of adenylate cyclase and are fully active after heating at 90 degrees for 5 min (pH 7).

Citing Articles

Comparison of effects of nicked and unnicked Escherichia coli heat-labile enterotoxin on Chinese hamster ovary cells.

Tsuji T, Honda T, MIWATANI T Infect Immun. 1984; 46(1):94-7.

PMID: 6384049 PMC: 261426. DOI: 10.1128/iai.46.1.94-97.1984.


Internalization and degradation of cholera toxin by cultured cells: relationship to toxin action.

Fishman P J Cell Biol. 1982; 93(3):860-5.

PMID: 6288736 PMC: 2112153. DOI: 10.1083/jcb.93.3.860.


Mechanism of action of choleragen and E. coli heat-labile enterotoxin: activation of adenylate cyclase by ADP-ribosylation.

Moss J, Vaughan M Mol Cell Biochem. 1981; 37(2):75-90.

PMID: 6268961 DOI: 10.1007/BF02354931.


Activity of covalently cross-linked cholera toxin with the adenylate cyclase of intact and lysed pigeon erythrocytes.

van Heyningen S Biochem J. 1977; 168(3):457-63.

PMID: 606247 PMC: 1183793. DOI: 10.1042/bj1680457.


The adenylate cyclase-activating activity of cholera toxin is not associated with a nicotinamide--adenine dinucleotide glycohydrolase activity.

Tait R, van Heyningen S Biochem J. 1978; 174(3):1059-62.

PMID: 215119 PMC: 1186012. DOI: 10.1042/bj1741059.


References
1.
Rifkind D, Frey J, Petersen E, Dinowitz M . Delayed hypersensitivity to fungal antigens in mice. II. Molecular classes in immunogenic RNA extracts that transfer delayed hypersensitivity. J Infect Dis. 1976; 133(5):523-32. DOI: 10.1093/infdis/133.5.523. View

2.
Gill D . Involvement of nicotinamide adenine dinucleotide in the action of cholera toxin in vitro. Proc Natl Acad Sci U S A. 1975; 72(6):2064-8. PMC: 432694. DOI: 10.1073/pnas.72.6.2064. View

3.
Gill D . Multiple roles of erythrocyte supernatant in the activation of adenylate cyclase by Vibrio cholerae toxin in vitro. J Infect Dis. 1976; 133 Suppl:55-63. DOI: 10.1093/infdis/133.supplement_1.s55. View

4.
Bitensky M, Wheeler M, Mehta H, Miki N . Cholera toxin activation of adenylate cyclase in cancer cell membrane fragments. Proc Natl Acad Sci U S A. 1975; 72(7):2572-6. PMC: 432811. DOI: 10.1073/pnas.72.7.2572. View

5.
van Heyningen S, King C . Short communications. Subunit A from cholera toxin is an activator of adenylate cyclase in pigeon erythrocytes. Biochem J. 1975; 146(1):269-71. PMC: 1165296. DOI: 10.1042/bj1460269. View