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Prospective Use of Brown Spider Venom Toxins as Therapeutic and Biotechnological Inputs.
Gremski, Luiza Helena; Matsubara, Fernando Hitomi; Polli, Nayanne Louise Costacurta; Antunes, Bruno Cesar; Schluga, Pedro Henrique de Caires; da Justa, Hanna Câmara; Minozzo, João Carlos; Wille, Ana Carolina Martins; Senff-Ribeiro, Andrea; Veiga, Silvio Sanches.
Afiliação
  • Gremski LH; Department of Cell Biology, Federal University of Paraná, Curitiba, Brazil.
  • Matsubara FH; Department of Cell Biology, Federal University of Paraná, Curitiba, Brazil.
  • Polli NLC; Department of Cell Biology, Federal University of Paraná, Curitiba, Brazil.
  • Antunes BC; Department of Cell Biology, Federal University of Paraná, Curitiba, Brazil.
  • Schluga PHC; Production and Research Center of Immunobiological Products, State Department of Health, Piraquara, Brazil.
  • da Justa HC; Department of Cell Biology, Federal University of Paraná, Curitiba, Brazil.
  • Minozzo JC; Department of Cell Biology, Federal University of Paraná, Curitiba, Brazil.
  • Wille ACM; Production and Research Center of Immunobiological Products, State Department of Health, Piraquara, Brazil.
  • Senff-Ribeiro A; Department of Structural, Molecular Biology and Genetics, State University of Ponta Grossa, Ponta Grossa, Brazil.
  • Veiga SS; Department of Cell Biology, Federal University of Paraná, Curitiba, Brazil.
Front Mol Biosci ; 8: 706704, 2021.
Article em En | MEDLINE | ID: mdl-34222343
ABSTRACT
Brown spider (genus Loxosceles) venoms are mainly composed of protein toxins used for predation and defense. Bites of these spiders most commonly produce a local dermonecrotic lesion with gravitational spread, edema and hemorrhage, which together are defined as cutaneous loxoscelism. Systemic loxoscelism, such as hematological abnormalities and renal injury, are less frequent but more lethal. Some Loxosceles venom toxins have already been isolated and extensively studied, such as phospholipases D (PLDs), which have been recombinantly expressed and were proven to reproduce toxic activities associated to the whole venom. PLDs have a notable potential to be engineered and converted in non-toxic antigens to produce a new generation of antivenoms or vaccines. PLDs also can serve as tools to discover inhibitors to be used as therapeutic agents. Other Loxosceles toxins have been identified and functionally characterized, such as hyaluronidases, allergen factor, serpin, TCTP and knottins (ICK peptides). All these toxins were produced as recombinant molecules and are biologically active molecules that can be used as tools for the potential development of chemical candidates to tackle many medical and biological threats, acting, for instance, as antitumoral, insecticides, analgesic, antigens for allergy tests and biochemical reagents for cell studies. In addition, these recombinant toxins may be useful to develop a rational therapy for loxoscelism. This review summarizes the main candidates for the development of drugs and biotechnological inputs that have been described in Brown spider venoms.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Front Mol Biosci Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Brasil

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Front Mol Biosci Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Brasil