Abstract

Snake venoms are rich sources of proteins with potential biotechnological and pharmaceutical applications. Among them, metalloproteases (MPs) and phospholipases A2 (PLA2) are the most abundant. Their isolation involves a multistep chromatographic approach, which has proven to be effective, however implies high operating costs and long processing times. In this study, a cost-effective and simple method based on aqueous two-phase systems (ATPS) was developed to recover MPs and PLA2 from Crotalus molossus nigrescens venom. A system with PEG 400 g mol−1, volume ratio (VR) 1, tie line length (TLL) 25% w/w and pH 7 showed the best performance for PLA2 recovery. In systems with PEG 400 g mol−1, VR 1, TLL 15% w/w, pH 7 and 1 and 3% w/w of NaCl, selective recovery of MP subtype P-III was achieved; whereas, in a system with PEG 400 g mol−1, VR 1, TLL 25% w/w and pH 8.5, MP subtypes P-I and P-III were recovered. Due to their low costs, ethanol–salt systems were also evaluated, however, failed to differentially partition PLA2 and MPs. The use of ATPS could contribute to the simplification and cost reduction of protein isolation processes from snake venoms and other toxin fluids, as well as potentially aid their biochemical, proteomic and biological analyses.Graphic

Highlights

  • Snake venoms are complex toxin cocktails comprising enzymatic and non-enzymatic proteins, such as phospholipases A2 (­Phos‐ pholipases A2 (PLA2)), metalloproteases (MPs), serine proteases (SPs), cysteine-rich secreted proteins, L-amino acid oxidases, C-type lectins, myotoxins, disintegrins, natriuretic peptides, hyaluronidases, nucleosidases and growth factors (Mackessy 2009)

  • Among its components, ­PLA2 and MPs have been identified as the most abundant, playing a primary role in many deleterious effects of snake envenomation (Tasoulis and Isbister 2017). The study of these toxins is of growing interest for biotechnological and pharmaceutical applications, as they can be used for antivenom design, development of new drugs, and elucidation of the mechanism of action of venoms (De Marco Almeida et al 2015; Gutiérrez et al 2017; Laustsen 2018; Bermúdez-Méndez et al 2018)

  • Aqueous two-phase systems (ATPS) have demonstrated to be useful as a partial recovery first step in downstream processes since it allows to remove a large quantity of contaminants

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Summary

Introduction

Snake venoms are complex toxin cocktails comprising enzymatic and non-enzymatic proteins, such as phospholipases A2 (­PLA2), metalloproteases (MPs), serine proteases (SPs), cysteine-rich secreted proteins, L-amino acid oxidases, C-type lectins, myotoxins, disintegrins, natriuretic peptides, hyaluronidases, nucleosidases and growth factors (Mackessy 2009). Among its components, ­PLA2 and MPs have been identified as the most abundant, playing a primary role in many deleterious effects of snake envenomation (Tasoulis and Isbister 2017). The study of these toxins is of growing interest for biotechnological and pharmaceutical applications, as they can be used for antivenom design, development of new drugs, and elucidation of the mechanism of action of venoms (De Marco Almeida et al 2015; Gutiérrez et al 2017; Laustsen 2018; Bermúdez-Méndez et al 2018). ATPS have been incorporated as pre-purification steps of different monoclonal antibodies from transgenic tobacco (Platis and Labrou 2009)

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