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A multiomics approach unravels new toxins with possible in silico antimicrobial, antiviral, and antitumoral activities in the venom of Acanthoscurria rondoniae
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor | (LETA) Lab. Toxinologia Aplicada | pt_BR |
dc.contributor | (CeTICS) Centro de Toxinas, Resposta-imune e Sinalização Celular | pt_BR |
dc.contributor.author | Câmara, Guilherme A. | pt_BR |
dc.contributor.author | Nishiyama Junior, Milton Yutaka | pt_BR |
dc.contributor.author | Kitano, Eduardo S. | pt_BR |
dc.contributor.author | Oliveira, Ursula Castro de | pt_BR |
dc.contributor.author | Silva Junior, Pedro Ismael da | pt_BR |
dc.contributor.author | Junqueira-de-Azevedo, Inácio de Loiola Meirelles | pt_BR |
dc.contributor.author | Tashima, Alexandre Keiji | pt_BR |
dc.date.accessioned | 2020-08-12T19:58:29Z | - |
dc.date.available | 2020-08-12T19:58:29Z | - |
dc.date.issued | 2020 | pt_BR |
dc.identifier.citation | Câmara GA., Nishiyama Junior MY, Kitano ES., Oliveira UC, Silva Junior PI, Junqueira-de-Azevedo ILM, et al. A multiomics approach unravels new toxins with possible in silico antimicrobial, antiviral, and antitumoral activities in the venom of Acanthoscurria rondoniae. Front. Pharmacol.. v. 11, 1075, jul. 2020. doi:10.3389/fphar.2020.01075. | pt_BR |
dc.identifier.uri | https://repositorio.butantan.gov.br/handle/butantan/3130 | - |
dc.description.abstract | The Araneae order is considered one of the most successful groups among venomous animals in the world. An important factor for this success is the production of venoms, a refined biological fluid rich in proteins, short peptides and cysteine-rich peptides (CRPs). These toxins may present pharmacologically relevant biological actions, as antimicrobial, antiviral and anticancer activities, for instance. Therefore, there is an increasing interest in the exploration of venom toxins for therapeutic reasons, such as drug development. However, the process of peptide sequencing and mainly the evaluation of potential biological activities of these peptides are laborious, considering the low yield of venom extraction and the high variability of toxins present in spider venoms. Here we show a robust methodology for identification, sequencing, and initial screening of potential bioactive peptides found in the venom of Acanthoscurria rondoniae. This methodology consists in a multiomics approach involving proteomics, peptidomics and transcriptomics analyses allied to in silico predictions of antibacterial, antifungal, antiviral, and anticancer activities. Through the application of this strategy, a total of 92,889 venom gland transcripts were assembled and 84 novel toxins were identified at the protein level, including seven short peptides and 10 fully sequenced CRPs (belonging to seven toxin families). In silico analysis suggests that seven CRPs families may have potential antimicrobial or antiviral activities, while two CRPs and four short peptides are potentially anticancer. Taken together, our results demonstrate an effective multiomics strategy for the discovery of new toxins and in silico screening of potential bioactivities. This strategy may be useful in toxin discovery, as well as in the screening of possible activities for the vast diversity of molecules produced by venomous animals. | pt_BR |
dc.description.sponsorship | (FAPESP) Fundação de Amparo à Pesquisa do Estado de São Paulo | pt_BR |
dc.description.sponsorship | (FINEP) Financiadora de Estudos e Projetos | pt_BR |
dc.description.sponsorship | (CAPES) Coordenação de Aperfeiçoamento de Pessoal de Nível Superior | pt_BR |
dc.format.extent | 1075 | pt_BR |
dc.language.iso | English | pt_BR |
dc.relation.ispartof | Frontiers in Pharmacology | pt_BR |
dc.rights | Open access | pt_BR |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | pt_BR |
dc.title | A multiomics approach unravels new toxins with possible in silico antimicrobial, antiviral, and antitumoral activities in the venom of Acanthoscurria rondoniae | pt_BR |
dc.type | Article | pt_BR |
dc.rights.license | CC BY | pt_BR |
dc.identifier.doi | 10.3389/fphar.2020.01075 | pt_BR |
dc.identifier.url | https://doi.org/10.3389/fphar.2020.01075 | pt_BR |
dc.contributor.external | (UNIFESP) Universidade Federal de São Paulo | pt_BR |
dc.contributor.external | (USP) Universidade de São Paulo | pt_BR |
dc.identifier.citationvolume | 11 | pt_BR |
dc.subject.keyword | Acanthoscurria rondoniae | pt_BR |
dc.subject.keyword | cysteine-rich peptides | pt_BR |
dc.subject.keyword | peptidomics | pt_BR |
dc.subject.keyword | proteomics | pt_BR |
dc.subject.keyword | multiomics | pt_BR |
dc.subject.keyword | antimicrobial peptides | pt_BR |
dc.subject.keyword | antiviral peptides | pt_BR |
dc.subject.keyword | antitumoral peptides | pt_BR |
dc.relation.ispartofabbreviated | Front Pharmacol | pt_BR |
dc.identifier.citationvancouver | 2020 July;11:1075 | pt_BR |
dc.contributor.butantan | Nishiyama Junior, Milton Yutaka|:Pesquisador|:(LETA) Lab. Toxinologia Aplicada:Centro de Toxinas, Resposta-imune e Sinalização Celular (CeTICS) | pt_BR |
dc.contributor.butantan | Oliveira, Ursula Castro de|:Aluno|:(LETA) Lab. Toxinologia Aplicada:Centro de Toxinas, Resposta-imune e Sinalização Celular (CeTICS) | pt_BR |
dc.contributor.butantan | Silva Junior, Pedro Ismael da|:Pesquisador|:(LETA) Lab. Toxinologia Aplicada:Centro de Toxinas, Resposta-imune e Sinalização Celular (CeTICS) | pt_BR |
dc.contributor.butantan | Junqueira-de-Azevedo, Inácio de Loiola Meirelles|:Pesquisador:Docente Permanente PPGTOX|:(LETA) Lab. Toxinologia Aplicada:Centro de Toxinas, Resposta-imune e Sinalização Celular (CeTICS) | pt_BR |
dc.contributor.butantan | Tashima, Alexandre Keiji|:Aluno|:(LETA) Lab. Toxinologia Aplicada:Centro de Toxinas, Resposta-imune e Sinalização Celular (CeTICS)|:Autor de correspondência | pt_BR |
dc.sponsorship.butantan | (FAPESP) Fundação de Amparo à Pesquisa do Estado de São Paulo¦¦2017/23771-3 | pt_BR |
dc.sponsorship.butantan | (FAPESP) Fundação de Amparo à Pesquisa do Estado de São Paulo¦¦2013/07467-1 | pt_BR |
dc.sponsorship.butantan | (FAPESP) Fundação de Amparo à Pesquisa do Estado de São Paulo¦¦2016/03839-0 | pt_BR |
dc.sponsorship.butantan | (FAPESP) Fundação de Amparo à Pesquisa do Estado de São Paulo¦¦2017/20106-9 | pt_BR |
dc.sponsorship.butantan | Financiadora de Estudos e Projetos (FINEP) | pt_BR |
dc.sponsorship.butantan | (CAPES) Coordenação de Aperfeiçoamento de Pessoal de Nível Superior | pt_BR |
dc.identifier.bvscc | BR78.1 | pt_BR |
dc.identifier.bvsdb | IBProd | pt_BR |
dc.description.dbindexed | Yes | pt_BR |
item.languageiso639-1 | English | - |
item.grantfulltext | open | - |
item.fulltext | Com Texto completo | - |
item.openairetype | Article | - |
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