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Toxicon ; 56(1): 55-63, 2010 Aug 01.
Article in English | MEDLINE | ID: mdl-20331995

ABSTRACT

Neurotoxicity is a major symptom of envenomation caused by Brazilian coral snake Micrurus frontalis. Due to the small amount of material that can be collected, no neurotoxin has been fully sequenced from this venom. In this work we report six new three-finger like toxins isolated from the venom of the coral snake M. frontalis which we named Frontoxin (FTx) I-VI. Toxins were purified using multiple steps of RP-HPLC. Molecular masses were determined by MALDI-TOF and ESI ion-trap mass spectrometry. The complete amino acid sequence of FTx II, III, IV and V were determined by sequencing of overlapping proteolytic fragments by Edman degradation and by de novo sequencing. The amino acid sequences of FTx I, II, III and VI predict 4 conserved disulphide bonds and structural similarity to previously reported short-chain alpha-neurotoxins. FTx IV and V each contained 10 conserved cysteines and share high similarity with long-chain alpha-neurotoxins. At the frog neuromuscular junction FTx II, III and IV reduced miniature endplate potential amplitudes in a time-and concentration-dependent manner suggesting Frontoxins block nicotinic acetylcholine receptors.


Subject(s)
Elapid Venoms/chemistry , Elapidae , Miniature Postsynaptic Potentials/drug effects , Motor Endplate/drug effects , Neurotoxins/toxicity , Reptilian Proteins/toxicity , Alkylation , Amino Acid Sequence , Animals , Chemical Fractionation , Cysteine/analysis , Elapid Venoms/toxicity , In Vitro Techniques , Molecular Sequence Data , Molecular Weight , Motor Endplate/physiology , Neurotoxins/chemistry , Neurotoxins/isolation & purification , Neurotoxins/metabolism , Osmolar Concentration , Oxidation-Reduction , Pectoralis Muscles/drug effects , Pectoralis Muscles/physiology , Peptide Fragments/chemistry , Peptide Fragments/isolation & purification , Protein Isoforms/chemistry , Protein Isoforms/isolation & purification , Protein Isoforms/metabolism , Protein Isoforms/toxicity , Rana catesbeiana , Reptilian Proteins/chemistry , Reptilian Proteins/isolation & purification , Reptilian Proteins/metabolism , Sequence Alignment
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