Volume 53, Issue 3 pp. 966-968
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Isolated Light Chain of Tetanus Toxin Inhibits Exocytosis: Studies in Digitonin-Permeabilized Cells

Mary A. Bittner

Corresponding Author

Mary A. Bittner

Department of Pharmacology, University of Michigan Medical School, Ann Arbor, Michigan;

Address correspondence and reprint requests to Dr. M. A. Bittner at M6322 Medical Science Building I, Department of Pharmacology, University of Michigan Medical School, Ann Arbor, MI 48109–0626, U.S.A.Search for more papers by this author
William H. Habig

William H. Habig

Laboratory of Bacterial Toxins, Division of Bacterial Products, U.S. Food and Drug Administration, Bethesda, Maryland, U.S.A.

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Ronald W. Holz

Ronald W. Holz

Department of Pharmacology, University of Michigan Medical School, Ann Arbor, Michigan;

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First published: September 1989
Citations: 53

Abstract

Previous work indicates that the heavy chain of tetanus toxin is responsible for the binding of the toxin to the neuronal membrane and its subsequent internalization. In the present study, the light chain of tetanus toxin mimicked the holotoxin in inhibiting Ca2+-dependent secretion of [3H]norepinephrine from digitonin-permeabilized adrenal chromaffin cells. Preincubation of tetanus toxin with monoclonal antibodies to the light chain prevented the inhibition by tetanus toxin. Preincubation of tetanus toxin with nonimmune ascites fluid or with monoclonal antibodies directed against the C fragment (the C-terminal of the heavy chains or the heavy-chain portion of the B fragment did not prevent inhibition by tetanus toxin. The data indicate that the light chain is responsible for the intracellular blockade of exostosis.

Abbreviations used:

  • kDa
  • kilodalton
  • KGEP
  • potassium glutamate-, EGTA-, and PIPES-containing solution
  • PIPES
  • piperazine-N, N”-bis(2-ethanesulfonic acid).
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