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PMID: 6929533 Published · ppublish English Journal Article

Binding of diphtheria toxin to phospholipids in liposomes.

Alving CR, Iglewski BH, Urban KA, Moss J, Richards RL, Sadoff JC

Abstract

Diphtheria toxin bound to the phosphate portion of some, but not all, phospholipids in liposomes. Liposomes consisting of dimyristoyl phosphatidylcholine and cholesterol did not bind toxin. Addition of 20 mol% (compared to dimyristoyl phosphatidylcholine) of dipalmitoyl phosphatidic acid, dicetyl phosphate, phosphatidylinositol phosphate, cardiolipin, or phosphatidylserine in the liposomes resulted in substantial binding of toxin. Inclusion of phosphatidylinositol in dimyristol phosphatidylcholine/cholesterol liposomes did not result in toxin binding. The calcium salt of dipalmitoyl phosphatidic acid was more effective than the sodium salt, and the highest level of binding occurred with liposomes consisting only of dipalmitoyl phosphatidic acid (calcium salt) and cholesterol. Binding of toxin to liposomes was dependent on pH, and the pattern of pH dependence varied with liposomes having different compositions. Incubation of diphtheria toxin with liposomes containing dicetyl phosphate resulted in maximal binding at pH 3.6, whereas binding to liposomes containing phosphatidylinositol phosphate was maximal above pH 7. Toxin did not bind to liposomes containing 20 mol% of a free fatty acid (palmitic acid) or a sulfated lipid (3-sulfogalactosylceramide). Toxin binding to dicetyl phosphate or phosphatidylinositol phosphate was inhibited by UTP, ATP, phosphocholine, or p-nitrophenyl phosphate, but not by uracil. We conclude that (a) diphtheria toxin binds specifically to the phosphate portion of certain phospholipids, (b) binding to phospholipids in liposomes is dependent on pH, but is not due only to electrostatic interaction, and (c) binding may be strongly influenced by the composition of adjacent phospholipids that do not bind toxin. We propose that a minor membrane phospholipid (such as phosphatidylinositol phosphate or phosphatidic acid), or that some other phosphorylated membrane molecule (such as a phosphoprotein) may be important in the initial binding of diphtheria toxin to cells.

MeSH Terms
Cardiolipins/metabolism Cholesterol/metabolism Diphtheria Toxin/metabolism Hydrogen-Ion Concentration Liposomes Nucleotides/pharmacology Organophosphates Organophosphorus Compounds/metabolism Phosphates/metabolism Phosphatidylcholines/metabolism Phospholipids/metabolism Receptors, Drug/metabolism Structure-Activity Relationship
Chemicals
Cardiolipins Diphtheria Toxin Liposomes Nucleotides Organophosphates Organophosphorus Compounds Phosphates Phosphatidylcholines Phospholipids Receptors, Drug dicetylphosphate Cholesterol
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Alving C R
Iglewski B H
Urban K A
Moss J
Richards R L
Sadoff J C
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31 references, click to expand
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1980-04-00
Pages
1986-90
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC348635
Subset
IM
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