Isolation, characterization and in silico study of propenamide alkaloids from Hymenoepmecis bicolor poison against active μ-opioid receptor
Some insects produce venoms to defend against predators and directly interact with opioid receptors. In the present study, it was identified two alkaloids in the wasp venom species Hymenoepimecis bicolor. It was demonstrated that these could act as potential inhibitors of opioid receptors through th...
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| Published in: | Journal of biomolecular structure & dynamics Vol. 41; no. 24; pp. 14621 - 14637 |
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| Main Authors: | , , , , , , , , , , |
| Format: | Journal Article |
| Language: | English |
| Published: |
England
Taylor & Francis
29.12.2023
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| ISSN: | 0739-1102, 1538-0254, 1538-0254 |
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| Abstract | Some insects produce venoms to defend against predators and directly interact with opioid receptors. In the present study, it was identified two alkaloids in the wasp venom species Hymenoepimecis bicolor. It was demonstrated that these could act as potential inhibitors of opioid receptors through their robust affinity to the receptors. The interaction profile was given to opioid receptors (μOR), with 60% of targets similar to alkaloid 1, with 0.25 probability, and 46.7% of targets similar to alkaloid 2, with a probability 0.17 of affinity as a target, which is considered signaling macromolecules and can mediate the most potent analgesic and addictive properties of opiate alkaloids. Notably, both alkaloids showed −7.6 kcal/mol affinity to the morphine agonies through six residues, Gly124, Asp147, Trp293, Ile296, Ile322, and Tyr326. These observations suggest further research on opioid receptors using in vitro studies of possible therapeutic applications.
Communicated by Ramaswamy H. Sarma |
|---|---|
| AbstractList | Some insects produce venoms to defend against predators and directly interact with opioid receptors. In the present study, it was identified two alkaloids in the wasp venom species
. It was demonstrated that these could act as potential inhibitors of opioid receptors through their robust affinity to the receptors. The interaction profile was given to opioid receptors (μOR), with 60% of targets similar to alkaloid 1, with 0.25 probability, and 46.7% of targets similar to alkaloid 2, with a probability 0.17 of affinity as a target, which is considered signaling macromolecules and can mediate the most potent analgesic and addictive properties of opiate alkaloids. Notably, both alkaloids showed -7.6 kcal/mol affinity to the morphine agonies through six residues, Gly124, Asp147, Trp293, Ile296, Ile322, and Tyr326. These observations suggest further research on opioid receptors using
studies of possible therapeutic applications.Communicated by Ramaswamy H. Sarma. Some insects produce venoms to defend against predators and directly interact with opioid receptors. In the present study, it was identified two alkaloids in the wasp venom species Hymenoepimecis bicolor. It was demonstrated that these could act as potential inhibitors of opioid receptors through their robust affinity to the receptors. The interaction profile was given to opioid receptors (μOR), with 60% of targets similar to alkaloid 1, with 0.25 probability, and 46.7% of targets similar to alkaloid 2, with a probability 0.17 of affinity as a target, which is considered signaling macromolecules and can mediate the most potent analgesic and addictive properties of opiate alkaloids. Notably, both alkaloids showed −7.6 kcal/mol affinity to the morphine agonies through six residues, Gly124, Asp147, Trp293, Ile296, Ile322, and Tyr326. These observations suggest further research on opioid receptors using in vitro studies of possible therapeutic applications. Communicated by Ramaswamy H. Sarma Some insects produce venoms to defend against predators and directly interact with opioid receptors. In the present study, it was identified two alkaloids in the wasp venom species Hymenoepimecis bicolor. It was demonstrated that these could act as potential inhibitors of opioid receptors through their robust affinity to the receptors. The interaction profile was given to opioid receptors (μOR), with 60% of targets similar to alkaloid 1, with 0.25 probability, and 46.7% of targets similar to alkaloid 2, with a probability 0.17 of affinity as a target, which is considered signaling macromolecules and can mediate the most potent analgesic and addictive properties of opiate alkaloids. Notably, both alkaloids showed -7.6 kcal/mol affinity to the morphine agonies through six residues, Gly124, Asp147, Trp293, Ile296, Ile322, and Tyr326. These observations suggest further research on opioid receptors using in vitro studies of possible therapeutic applications.Communicated by Ramaswamy H. Sarma.Some insects produce venoms to defend against predators and directly interact with opioid receptors. In the present study, it was identified two alkaloids in the wasp venom species Hymenoepimecis bicolor. It was demonstrated that these could act as potential inhibitors of opioid receptors through their robust affinity to the receptors. The interaction profile was given to opioid receptors (μOR), with 60% of targets similar to alkaloid 1, with 0.25 probability, and 46.7% of targets similar to alkaloid 2, with a probability 0.17 of affinity as a target, which is considered signaling macromolecules and can mediate the most potent analgesic and addictive properties of opiate alkaloids. Notably, both alkaloids showed -7.6 kcal/mol affinity to the morphine agonies through six residues, Gly124, Asp147, Trp293, Ile296, Ile322, and Tyr326. These observations suggest further research on opioid receptors using in vitro studies of possible therapeutic applications.Communicated by Ramaswamy H. Sarma. |
| Author | Gaieta, Eduardo Menezes Colares, Regilany Paulo Barbosa da Silva, Francisco Lennon Marinho, Emmanuel Silva Sobczak, Jober Fernando Caluaco, Bernardino Joaquim dos Santos, Hélcio Silva Freire da Silva, Ananias Marques da Fonseca, Aluísio Nunes da Rocha, Matheus Marinho, Gabrielle Silva |
| Author_xml | – sequence: 1 givenname: Aluísio orcidid: 0000-0002-8112-9513 surname: Marques da Fonseca fullname: Marques da Fonseca, Aluísio organization: Institute of Exact Sciences and Nature, University of International Integration of Afro-Brazilian Lusophony – sequence: 2 givenname: Ananias surname: Freire da Silva fullname: Freire da Silva, Ananias organization: Institute of Engineering and Sustainable Development, University of International Integration of Afro-Brazilian Lusofonia – sequence: 3 givenname: Francisco Lennon surname: Barbosa da Silva fullname: Barbosa da Silva, Francisco Lennon organization: Institute of Engineering and Sustainable Development, University of International Integration of Afro-Brazilian Lusofonia – sequence: 4 givenname: Bernardino Joaquim surname: Caluaco fullname: Caluaco, Bernardino Joaquim organization: Institute of Exact Sciences and Nature, University of International Integration of Afro-Brazilian Lusophony – sequence: 5 givenname: Eduardo Menezes surname: Gaieta fullname: Gaieta, Eduardo Menezes organization: Institute of Exact Sciences and Nature, University of International Integration of Afro-Brazilian Lusophony – sequence: 6 givenname: Matheus orcidid: 0000-0002-0929-4565 surname: Nunes da Rocha fullname: Nunes da Rocha, Matheus organization: Faculty of Philosophy Dom Aureliano Matos, State University of Ceará – sequence: 7 givenname: Regilany Paulo orcidid: 0000-0001-5679-1575 surname: Colares fullname: Colares, Regilany Paulo organization: Institute of Exact Sciences and Nature, University of International Integration of Afro-Brazilian Lusophony – sequence: 8 givenname: Jober Fernando surname: Sobczak fullname: Sobczak, Jober Fernando organization: Institute of Exact Sciences and Nature, University of International Integration of Afro-Brazilian Lusophony – sequence: 9 givenname: Gabrielle Silva orcidid: 0000-0001-8950-7497 surname: Marinho fullname: Marinho, Gabrielle Silva organization: Faculty of Philosophy Dom Aureliano Matos, State University of Ceará – sequence: 10 givenname: Hélcio Silva orcidid: 0000-0001-5527-164X surname: dos Santos fullname: dos Santos, Hélcio Silva organization: Department of Biological Chemistry, Regional University of Cariri – sequence: 11 givenname: Emmanuel Silva orcidid: 0000-0002-4774-8775 surname: Marinho fullname: Marinho, Emmanuel Silva organization: Faculty of Philosophy Dom Aureliano Matos, State University of Ceará |
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| SubjectTerms | Alkaloids - pharmacology arthropod chemical composition computational simulation Morphine - chemistry Morphine - pharmacology Poisons Receptors, Opioid Wasp |
| Title | Isolation, characterization and in silico study of propenamide alkaloids from Hymenoepmecis bicolor poison against active μ-opioid receptor |
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