Abstract |
Cobra venom contains cardiotoxins (CTXs) that induce tissue necrosis and systolic heart arrest in bitten victims. CTX-induced membrane pore formation is one of the major mechanisms responsible for the venom's designated cytotoxicity. This chapter examines how glycoconjugates such as heparan sulfates (HS) and glycosphingolipids, located respectively in the extracellular matrix and lipid bilayers of the cell membranes, facilitate CTX pore formation. Evidences for HS-facilitated cell surface retention and glycosphingolipid-facilitated membrane bilayer insertion of CTX are reviewed. We suggest that similar physical steps could play a role in the mediation of other pore forming toxins (PFT). The membrane pores formed by PFT are expected to have limited lifetime on biological cell surface as a result of membrane dynamics during endocytosis and/or rearrangement of lipid rafts.
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Authors | Wen-Guey Wu, Siu-Cin Tjong, Po-Long Wu, Je-Hung Kuo, Karen Wu |
Journal | Advances in experimental medicine and biology
(Adv Exp Med Biol)
Vol. 677
Pg. 143-9
( 2010)
ISSN: 0065-2598 [Print] United States |
PMID | 20687487
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Review)
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Chemical References |
- Cobra Cardiotoxin Proteins
- Lipid Bilayers
- Pore Forming Cytotoxic Proteins
- Sphingolipids
- Heparitin Sulfate
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Topics |
- Animals
- Cobra Cardiotoxin Proteins
(chemistry, metabolism)
- Elapidae
- Heart Arrest
(metabolism)
- Heparitin Sulfate
(chemistry, metabolism)
- Humans
- Lipid Bilayers
(chemistry, metabolism)
- Membrane Microdomains
(chemistry, metabolism)
- Necrosis
(metabolism)
- Pore Forming Cytotoxic Proteins
(chemistry, metabolism)
- Sphingolipids
(chemistry, metabolism)
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