Cnidarian peptide neurotoxins: a new source of various ion channel modulators or blockers against central nervous systems disease
Liao, Q.; Feng, Y.; Yang, B.; Lee, S.M.-Y. (2019). Cnidarian peptide neurotoxins: a new source of various ion channel modulators or blockers against central nervous systems disease. Drug Discovery Today 24(1): 189-197. https://dx.doi.org/10.1016/j.drudis.2018.08.011
In: Drug Discovery Today. Elsevier SCI Ltd: Oxford. ISSN 1359-6446; e-ISSN 1878-5832, more
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| Authors | | Top |
- Liao, Q.
- Feng, Y.
- Yang, B.
- Lee, S.M.-Y.
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| Abstract |
Cnidaria provide the largest source of bioactive peptides for new drug development. The venoms contain enzymes, potent pore-forming toxins and neurotoxins. The neurotoxins can immobilize predators rapidly when discharged via modifying sodium-channel-gating or blocking the potassium channel during the repolarization stage. Most cnidarian neurotoxins remain conserved under the strong influence of negative selection. Neuroactive peptides targeting the central nervous system through affinity with ion channels could provide insight leading to drug treatment of neurological diseases, which arise from ion channel dysfunctions. Although marine resources offer thousands of possible peptides, only one peptide derived from Cnidaria: ShK-186, also named dalazatide, has reached the pharmaceutical market. This review focuses on neuroprotective agents derived from cnidarian neurotoxic peptides. |
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