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Open AccessJournal ArticleDOI

Purification of animal neurotoxins. Isolation and characterization of eleven neurotoxins from the venoms of the scorpions Androctonus australis hector, Buthus occitanus tunetanus and Leiurus quinquestriatus quinquestriatus.

TLDR
Using the same method of purification of small molecular weight proteins worked out to obtain pure scorpion neurotoxins, four neurotoxin have been isolated from the venom of the cobra Naja haje, suggesting that each venom originating from a different sub-species has a taxonomical counterpart.
Abstract
Using the same method of purification of small molecular weight proteins worked out to obtain pure scorpion neurotoxins, four neurotoxins have been isolated from the venom of the cobra Naja haje. N. haje venom from the Miami Serpentarium contains two neurotoxins (I and II) whereas the venom of the same species obtained from the Institut Pasteur contains three neurotoxins (I, II′ and III). Toxins I, II and II′ consist of 61 amino acid residues and toxin III of 71. All are basic proteins containing four or five disulphide bridges. It is likely that the difference observed in neurotoxin composition of N. haje venoms from two different sources has a taxonomical counterpart, each venom originating from a different sub-species.

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Citations
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Journal ArticleDOI

Bacterial toxins: a table of lethal amounts.

D M Gill
TL;DR: Risks Associated with Cloning Toxin Genes in Escherichia coli, and Recommended Containment Levels for Cloning, are discussed.
Journal ArticleDOI

Scorpion toxins specific for Na+-channels.

TL;DR: A classification containing 10 different groups of toxins is proposed in this review, based on functional and structural features of the known toxins, and the limited success obtained in the search for the site through which these peptides bind to the channels.
Journal ArticleDOI

Overview of scorpion toxins specific for Na+ channels and related peptides: biodiversity, structure-function relationships and evolution.

TL;DR: A critical view on problems associated with the study of these scorpion peptides is presented, drawing special attention to the points that need revision and to the subjects under intensive research at this moment, regarding scorpion toxins specific for Na(+) channels and the other related long-chain peptides recently described.
Journal ArticleDOI

The scorpion envenoming syndrome

M. Ismail
- 01 Jul 1995 - 
TL;DR: The pathophysiology of the scorpion envenoming syndrome is reviewed with emphasis on the body systems commonly affected and the pharmacokinetic characteristics of scorpion venoms and their correlation to the magnitude of toxic effects are presented in relation to the potentials of therapeutic intervention.
Journal ArticleDOI

Two types of scorpion neurotoxins characterized by their binding to two separate receptor sites on rat brain synaptosomes

TL;DR: A distinction between scorpion neurotoxins is proposed according to their binding properties to rat brain synaptosomes because of the 6–10 times more sites for Centruroides than for Androctonus neurotoxin.
References
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Journal ArticleDOI

Starch gel electrophoresis in a discontinous system of buffers.

TL;DR: Working on the separated and eluted fractions of the toxin of Corynebacterium diphtheriae in tissue cultures and in animals indicated that the resolution of these proteins was not completely satisfactory in the buffer.
Book ChapterDOI

[117] Chromatographic determination of amino acids by the use of automatic recording equipment

TL;DR: This chapter describes the chromatographic determination of amino acids by the use of automatic recording equipments and suggests that air-oxidation of cysteine in the hydrolyzate to cystine, before chromatography, is desirable in order to obtain a more accurate value for the total cyStine + cySteine content of the protein.
Book ChapterDOI

Ultraviolet absorption spectra of proteins and amino acids.

TL;DR: This chapter deals with the absorption spectra of proteins and amino acids, principally derived from the study of homogeneous absorbing systems, in which the inhomogeneity is finer in grade by several orders than the dimensions of the exploring light beam.
Journal ArticleDOI

A modified procedure for the automatic analysis of amino acids.

TL;DR: The procedure described allows the complete analysis of a protein hydrolyzate, including collagen, in 24 hr using a single sample, and is also suitable for many other biological amino acid mixtures.
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