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...

Full description

Bibliographic Details
Main Authors: 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
Format: Article
Language:English
Published: MDPI AG 2019-06-01
Series:Toxins
Subjects:
Online Access:https://www.mdpi.com/2072-6651/11/6/355
id doaj-8532f42aa4f9461e8b89dad90da1dc8a
record_format Article
spelling 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&#8722;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&#8722;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 AT danielechavesmoreira brownspideriloxoscelesivenomtoxinsaspotentialbiotoolsforthedevelopmentofnoveltherapeutics
AT fernandohitomimatsubara brownspideriloxoscelesivenomtoxinsaspotentialbiotoolsforthedevelopmentofnoveltherapeutics
AT zelindaschemczssengraeff brownspideriloxoscelesivenomtoxinsaspotentialbiotoolsforthedevelopmentofnoveltherapeutics
AT elidianadebona brownspideriloxoscelesivenomtoxinsaspotentialbiotoolsforthedevelopmentofnoveltherapeutics
AT vanessaribeiroheidemann brownspideriloxoscelesivenomtoxinsaspotentialbiotoolsforthedevelopmentofnoveltherapeutics
AT claraguerraduarte brownspideriloxoscelesivenomtoxinsaspotentialbiotoolsforthedevelopmentofnoveltherapeutics
AT luizahelenagremski brownspideriloxoscelesivenomtoxinsaspotentialbiotoolsforthedevelopmentofnoveltherapeutics
AT carloschavezolortegui brownspideriloxoscelesivenomtoxinsaspotentialbiotoolsforthedevelopmentofnoveltherapeutics
AT andreasenffribeiro brownspideriloxoscelesivenomtoxinsaspotentialbiotoolsforthedevelopmentofnoveltherapeutics
AT olgameirichaim brownspideriloxoscelesivenomtoxinsaspotentialbiotoolsforthedevelopmentofnoveltherapeutics
AT raghuvirkrishnaswamyarni brownspideriloxoscelesivenomtoxinsaspotentialbiotoolsforthedevelopmentofnoveltherapeutics
AT silviosanchesveiga brownspideriloxoscelesivenomtoxinsaspotentialbiotoolsforthedevelopmentofnoveltherapeutics
_version_ 1725004739012198400