2021
DOI: 10.1590/1678-9199-jvatitd-2020-0180
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P-I metalloproteinases and L-amino acid oxidases from Bothrops species inhibit angiogenesis

Abstract: Background: Snake venoms are composed of pharmacologically active proteins that are evolutionarily diverse, stable and specific to targets. Hence, venoms have been explored as a source of bioactive molecules in treating numerous diseases. Recent evidences suggest that snake venom proteins may affect the formation of new blood vessels. Excessive angiogenesis has been implicated in several pathologies including tumours, diabetic retinopathy, arthritis, inter alia . In the … Show more

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Cited by 7 publications
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“…AEX was used as a second chromatographic step for the purification of a metalloproteinase and L-amino acid oxidase from Bothrops atrox and Bothrops mojeni. To do so, fractions eluted from SEC were re-fractionated on a Mono Q column to reach the pure protein [19]. In another study, a DEAE-Sephacel AEX column was used as a first step to separate metalloproteinase from Bothrops moojeni and required two successive chromatographic techniques to reach the pure protein [20].…”
Section: Ion Exchange Chromatographymentioning
confidence: 99%
“…AEX was used as a second chromatographic step for the purification of a metalloproteinase and L-amino acid oxidase from Bothrops atrox and Bothrops mojeni. To do so, fractions eluted from SEC were re-fractionated on a Mono Q column to reach the pure protein [19]. In another study, a DEAE-Sephacel AEX column was used as a first step to separate metalloproteinase from Bothrops moojeni and required two successive chromatographic techniques to reach the pure protein [20].…”
Section: Ion Exchange Chromatographymentioning
confidence: 99%