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Cellular and Molecular Life Sciences CMLS

, Volume 60, Issue 11, pp 2409–2426 | Cite as

Pharmacologically active spider peptide toxins

  • G. Corzo
  • P. Escoubas
Review

Abstract

Advances in mass spectrometry and peptide biochemistry coupled to modern methods in electrophysiology have permitted the isolation and identification of numerous novel peptide toxins from animal venoms in recent years. These advances have also opened up the field of spider venom research, previously unexplored due to methodological limitations. Many peptide toxins from spider venoms share structural features, amino acid composition and consensus sequences that allow them to interact with related classes of cellular receptors. They have become increasingly useful agents for the study of voltage-sensitive and ligand-gated ion channels and the discrimination of their cellular subtypes. Spider peptide toxins have also been recognized as useful agents for their antimicrobial properties and the study of pore formation in cell membranes. Spider peptide toxins with nanomolar affinities for their receptors are thus promising pharmacological tools for understanding the physiological role of ion channels and as leads for the development of novel therapeutic agents and strategies for ion channel-related diseases. Their high insecticidal potency can also make them useful probes for the discovery of novel insecticide targets in the insect nervous system or for the development of genetically engineered microbial pesticides.

Spider peptide toxin insecticide structure pharmacology ion channel 

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Copyright information

© Birkhäuser-Verlag Basel 2003

Authors and Affiliations

  1. 1.Suntory Institute for Bioorganic ResearchMishima-Gun, Shimamoto-ChoOsaka
  2. 2.Institut de Pharmacologie Moléculaire et CellulaireCentre National de la Recherche ScientifiqueValbonne

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