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  Mechanisms of α-latrotoxin actin

Henkel, A. W., & Sankaranarayanan, S. (1999). Mechanisms of α-latrotoxin actin. Cell and Tissue Research, 296, 229-233. doi:10.1007/s004410051284.

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CellTissRes_296_1999_229.pdf (Any fulltext), 87KB
 
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 Creators:
Henkel, Andreas Wolfram1, Author           
Sankaranarayanan, S., Author
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1Department of Biomedical Optics, Max Planck Institute for Medical Research, Max Planck Society, ou_1497699              

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Free keywords: Black widow spider venom, Calcium-independent receptor for α-latrotoxin Exocytosis, G-proteins, Latrophilin, Neurexins, Chromaffin cells
 Abstract: The major component of black widow spider venom, α-latrotoxin, triggers massive exocytosis in a variety of neurosecretory cells. An important trigger for exocytosis is the calcium influx via α-latrotoxin-induced channels in biological membranes. However, this mechanism fails to explain exocytosis which occurred in the complete absence of extracellular calcium. Recently, sophisticated biochemical and molecular techniques have led to the discovery of novel α-latrotoxin-binding membrane receptors: neurexins and latrophilin/CIRL (calcium-independent receptor for α-latrotoxin). Neurexins are single transmembrane proteins which bind to α-latrotoxin in a calcium-dependent manner and also interact with the synaptic vesicle protein, synaptotagmin. On the other hand, latrophilin is a seven-transmembrane protein and belongs to the family of G-protein-coupled receptors. The multitude of effects of α-latrotoxin on exocytosis in different cell systems and the nature of its membrane targets are discussed in this article. The molecular details of how α-latrotoxin binding is transduced eventually to exocytosis remain to be elucidated

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Language(s): eng - English
 Dates: 1998-11-261998-10-231999-04-01
 Publication Status: Issued
 Pages: 5
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 Table of Contents: -
 Rev. Type: Peer
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Title: Cell and Tissue Research
Source Genre: Journal
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Publ. Info: Heidelberg : Springer-Verlag
Pages: - Volume / Issue: 296 Sequence Number: - Start / End Page: 229 - 233 Identifier: ISSN: 0302-766X
CoNE: https://pure.mpg.de/cone/journals/resource/991042749577550