Brown Spider (<i>Loxosceles</i>) Venom Toxins as Potential Biotools for the Development of Novel Therapeutics
Brown spider envenomation results in dermonecrosis with gravitational spreading characterized by a marked inflammatory reaction and with lower prevalence of systemic manifestations such as renal failure and hematological disturbances. Several toxins make up the venom of these species, and they are m...
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doaj-8532f42aa4f9461e8b89dad90da1dc8a2020-11-25T01:49:49ZengMDPI AGToxins2072-66512019-06-0111635510.3390/toxins11060355toxins11060355Brown Spider (<i>Loxosceles</i>) Venom Toxins as Potential Biotools for the Development of Novel TherapeuticsDaniele Chaves-Moreira0Fernando Hitomi Matsubara1Zelinda Schemczssen-Graeff2Elidiana De Bona3Vanessa Ribeiro Heidemann4Clara Guerra-Duarte5Luiza Helena Gremski6Carlos Chávez-Olórtegui7Andrea Senff-Ribeiro8Olga Meiri Chaim9Raghuvir Krishnaswamy Arni10Silvio Sanches Veiga11Departamento de Biologia Celular, Universidade Federal do Paraná (UFPR), Curitiba 81531-970, PR, BrazilDepartamento de Biologia Celular, Universidade Federal do Paraná (UFPR), Curitiba 81531-970, PR, BrazilDepartamento de Biologia Celular, Universidade Federal do Paraná (UFPR), Curitiba 81531-970, PR, BrazilDepartamento de Biologia Celular, Universidade Federal do Paraná (UFPR), Curitiba 81531-970, PR, BrazilDepartamento de Biologia Celular, Universidade Federal do Paraná (UFPR), Curitiba 81531-970, PR, BrazilDepartamento de Bioquímica e Imunologia, Universidade Federal de Minas Gerais (UFMG), Belo Horizonte 31270-901, MG, BrazilDepartamento de Biologia Celular, Universidade Federal do Paraná (UFPR), Curitiba 81531-970, PR, BrazilDepartamento de Bioquímica e Imunologia, Universidade Federal de Minas Gerais (UFMG), Belo Horizonte 31270-901, MG, BrazilDepartamento de Biologia Celular, Universidade Federal do Paraná (UFPR), Curitiba 81531-970, PR, BrazilDepartamento de Biologia Celular, Universidade Federal do Paraná (UFPR), Curitiba 81531-970, PR, BrazilCentro Multiusuário de Inovação Biomolecular, Departamento de Física, Universidade Estadual Paulista (UNESP), São José do Rio Preto 15054-000, SP, BrazilDepartamento de Biologia Celular, Universidade Federal do Paraná (UFPR), Curitiba 81531-970, PR, BrazilBrown spider envenomation results in dermonecrosis with gravitational spreading characterized by a marked inflammatory reaction and with lower prevalence of systemic manifestations such as renal failure and hematological disturbances. Several toxins make up the venom of these species, and they are mainly peptides and proteins ranging from 5−40 kDa. The venoms have three major families of toxins: phospholipases-D, astacin-like metalloproteases, and the inhibitor cystine knot (ICK) peptides. Serine proteases, serpins, hyaluronidases, venom allergens, and a translationally controlled tumor protein (TCTP) are also present. Toxins hold essential biological properties that enable interactions with a range of distinct molecular targets. Therefore, the application of toxins as research tools and clinical products motivates repurposing their uses of interest. This review aims to discuss possibilities for brown spider venom toxins as putative models for designing molecules likely for therapeutics based on the status quo of brown spider venoms. Herein, we explore new possibilities for the venom components in the context of their biochemical and biological features, likewise their cellular targets, three-dimensional structures, and mechanisms of action.https://www.mdpi.com/2072-6651/11/6/355brown spidervenomLoxoscelestoxinsbiotoolsdrug targetsnovel therapeutics |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Daniele Chaves-Moreira Fernando Hitomi Matsubara Zelinda Schemczssen-Graeff Elidiana De Bona Vanessa Ribeiro Heidemann Clara Guerra-Duarte Luiza Helena Gremski Carlos Chávez-Olórtegui Andrea Senff-Ribeiro Olga Meiri Chaim Raghuvir Krishnaswamy Arni Silvio Sanches Veiga |
spellingShingle |
Daniele Chaves-Moreira Fernando Hitomi Matsubara Zelinda Schemczssen-Graeff Elidiana De Bona Vanessa Ribeiro Heidemann Clara Guerra-Duarte Luiza Helena Gremski Carlos Chávez-Olórtegui Andrea Senff-Ribeiro Olga Meiri Chaim Raghuvir Krishnaswamy Arni Silvio Sanches Veiga Brown Spider (<i>Loxosceles</i>) Venom Toxins as Potential Biotools for the Development of Novel Therapeutics Toxins brown spider venom Loxosceles toxins biotools drug targets novel therapeutics |
author_facet |
Daniele Chaves-Moreira Fernando Hitomi Matsubara Zelinda Schemczssen-Graeff Elidiana De Bona Vanessa Ribeiro Heidemann Clara Guerra-Duarte Luiza Helena Gremski Carlos Chávez-Olórtegui Andrea Senff-Ribeiro Olga Meiri Chaim Raghuvir Krishnaswamy Arni Silvio Sanches Veiga |
author_sort |
Daniele Chaves-Moreira |
title |
Brown Spider (<i>Loxosceles</i>) Venom Toxins as Potential Biotools for the Development of Novel Therapeutics |
title_short |
Brown Spider (<i>Loxosceles</i>) Venom Toxins as Potential Biotools for the Development of Novel Therapeutics |
title_full |
Brown Spider (<i>Loxosceles</i>) Venom Toxins as Potential Biotools for the Development of Novel Therapeutics |
title_fullStr |
Brown Spider (<i>Loxosceles</i>) Venom Toxins as Potential Biotools for the Development of Novel Therapeutics |
title_full_unstemmed |
Brown Spider (<i>Loxosceles</i>) Venom Toxins as Potential Biotools for the Development of Novel Therapeutics |
title_sort |
brown spider (<i>loxosceles</i>) venom toxins as potential biotools for the development of novel therapeutics |
publisher |
MDPI AG |
series |
Toxins |
issn |
2072-6651 |
publishDate |
2019-06-01 |
description |
Brown spider envenomation results in dermonecrosis with gravitational spreading characterized by a marked inflammatory reaction and with lower prevalence of systemic manifestations such as renal failure and hematological disturbances. Several toxins make up the venom of these species, and they are mainly peptides and proteins ranging from 5−40 kDa. The venoms have three major families of toxins: phospholipases-D, astacin-like metalloproteases, and the inhibitor cystine knot (ICK) peptides. Serine proteases, serpins, hyaluronidases, venom allergens, and a translationally controlled tumor protein (TCTP) are also present. Toxins hold essential biological properties that enable interactions with a range of distinct molecular targets. Therefore, the application of toxins as research tools and clinical products motivates repurposing their uses of interest. This review aims to discuss possibilities for brown spider venom toxins as putative models for designing molecules likely for therapeutics based on the status quo of brown spider venoms. Herein, we explore new possibilities for the venom components in the context of their biochemical and biological features, likewise their cellular targets, three-dimensional structures, and mechanisms of action. |
topic |
brown spider venom Loxosceles toxins biotools drug targets novel therapeutics |
url |
https://www.mdpi.com/2072-6651/11/6/355 |
work_keys_str_mv |
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