2008
DOI: 10.1016/j.bbagen.2007.11.007
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Identification, cloning and functional characterization of a novel dermonecrotic toxin (phospholipase D) from brown spider (Loxosceles intermedia) venom

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Cited by 65 publications
(70 citation statements)
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“…This method was chosen because of its proven efficiency to evaluate the esphingomyelinase-D activity in bronw spider venom (Appel et al, 2008). Three concentrations of venom were tested (10, 30 e 100 mg/mL) but only the higher concentration increased the fluorescence intensity after 30 min of the reaction (Fig.…”
Section: Characterization Of Enzymatic Activities Of Loxosceles Intermentioning
confidence: 99%
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“…This method was chosen because of its proven efficiency to evaluate the esphingomyelinase-D activity in bronw spider venom (Appel et al, 2008). Three concentrations of venom were tested (10, 30 e 100 mg/mL) but only the higher concentration increased the fluorescence intensity after 30 min of the reaction (Fig.…”
Section: Characterization Of Enzymatic Activities Of Loxosceles Intermentioning
confidence: 99%
“…L. intermedia venom is liquid, colorless, crystalline and extremely rich in proteases, alkaline phosphatase, hyaluronidases, phospholipases, metalloproteases among other components (Barbaro et al, 2005;Chaim et al, 2011;da Silveira et al, 2007a;da Silveira et al, 2007b;Tambourgi et al, 2000). The spread of the venom and consequent dermonecrosis observed in humans and rabbits are attributed to hyaluronidase (Futrell, 1992) and phospholipase D (also referred as sphingomyelinase D) activities (Appel et al, 2008;Kalapothakis et al, 2007;Tambourgi et al, 1998). In fact, the occurrence of dermonecrosis at the site of inoculation of the venom is considered the most important clinical manifestation of loxoscelism (Hogan et al, 2004;Veiga et al, 2001;Zanetti et al, 2002).…”
Section: Introductionmentioning
confidence: 98%
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“…While enzymes are present in the majority of venoms [18][19][20][21][22][23][24][25][26][27][28], their number in invertebrates is very limited compared to that in snake venoms. As ArachnoServer and ConoServer deal with invertebrate proteins, data on enzymes are either limited, or nonexistent.…”
Section: Enzymesmentioning
confidence: 99%
“…The toxin was produced as described previously (Chaim et al, 2006;ChavesMoreira et al, 2011). The integrity, purity and quality of rLiD1 was checked by electrophoresis (Harlow and Lane, 1988) and its activity was measured using the Amplex Red Assay Kit (Molecular Probes, Eugene) as previously described (Appel et al, 2008;ChavesMoreira et al, 2011).…”
Section: Recombinant Toxin Phospholipase D(rlid1)mentioning
confidence: 99%