An in silico approach on the allergenicity and cross reactivity of the tropomyosin epitope of Oreochromis mossambicus

Analysis of the allergenicity and cross-reactivity of the tropomyosin epitope of Oreochromis mossambicus, also known as tilapia, was done via an in silico approach. Structural validation of Immunoglobulin E through Ramachandran Plot, ERRAT, and Verify 3D showed relatively high values, suggesting tha...

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Main Authors: Endozo, Rikki Noreen S., Kim, Abby Gayl A., San Jose, Juan Miguel
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Language:English
Published: Animo Repository 2022
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Online Access:https://animorepository.dlsu.edu.ph/etdb_physics/17
https://animorepository.dlsu.edu.ph/context/etdb_physics/article/1019/viewcontent/2022_SanJose_Endozo_Kim_An_in_silico_approach_on_the_allergenicity_Full_text.pdf
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spelling oai:animorepository.dlsu.edu.ph:etdb_physics-10192023-02-08T00:34:50Z An in silico approach on the allergenicity and cross reactivity of the tropomyosin epitope of Oreochromis mossambicus Endozo, Rikki Noreen S. Kim, Abby Gayl A. San Jose, Juan Miguel Analysis of the allergenicity and cross-reactivity of the tropomyosin epitope of Oreochromis mossambicus, also known as tilapia, was done via an in silico approach. Structural validation of Immunoglobulin E through Ramachandran Plot, ERRAT, and Verify 3D showed relatively high values, suggesting that the chosen protein for docking is a high-quality model. Intermolecular forces of attraction present in the IgE-Tropomyosin, viewed via BIOVIA Discovery Studio Visualizer, were mostly hydrogen bonds, electrostatic interactions, and hydrophobic interactions. Molecular Dynamics simulation performed through CABS-FLEX 2.0 demonstrates that no significant difference exists between the bound and unbound structures of the IgE-Tropomyosin complex. Only minor fluctuations were observable in the Root Mean Square Fluctuation plots of chains A and B, having p-values of 0.38 and 0.15, respectively. These results depict that the complex is stable enough for a strong binding. The tropomyosin epitope of tilapia had three identified allergenic sequences, and findings indicate that the following species, common in the Philippines, have 100 percent similarity with all three protein sequences: mud crab, giant tiger prawn, blue swimming crab, Atlantic white shrimp, brown shrimp, and white leg shrimp. Other species, such as three spot swimming crab, Crucifix crab, and giant freshwater prawn can also be found in the Philippines but are not considered common, based on the PSA data from 2017 to 2019. The stated species are suggestive of being cross-reactive with the tropomyosin of Oreochromis mossambicus, meaning it is highly probable that a person allergic to tilapia could also be allergic to the listed species of seafood. 2022-01-01T08:00:00Z text application/pdf https://animorepository.dlsu.edu.ph/etdb_physics/17 https://animorepository.dlsu.edu.ph/context/etdb_physics/article/1019/viewcontent/2022_SanJose_Endozo_Kim_An_in_silico_approach_on_the_allergenicity_Full_text.pdf Physics Bachelor's Theses English Animo Repository Mozambique tilapia Tropomyosins Physics
institution De La Salle University
building De La Salle University Library
continent Asia
country Philippines
Philippines
content_provider De La Salle University Library
collection DLSU Institutional Repository
language English
topic Mozambique tilapia
Tropomyosins
Physics
spellingShingle Mozambique tilapia
Tropomyosins
Physics
Endozo, Rikki Noreen S.
Kim, Abby Gayl A.
San Jose, Juan Miguel
An in silico approach on the allergenicity and cross reactivity of the tropomyosin epitope of Oreochromis mossambicus
description Analysis of the allergenicity and cross-reactivity of the tropomyosin epitope of Oreochromis mossambicus, also known as tilapia, was done via an in silico approach. Structural validation of Immunoglobulin E through Ramachandran Plot, ERRAT, and Verify 3D showed relatively high values, suggesting that the chosen protein for docking is a high-quality model. Intermolecular forces of attraction present in the IgE-Tropomyosin, viewed via BIOVIA Discovery Studio Visualizer, were mostly hydrogen bonds, electrostatic interactions, and hydrophobic interactions. Molecular Dynamics simulation performed through CABS-FLEX 2.0 demonstrates that no significant difference exists between the bound and unbound structures of the IgE-Tropomyosin complex. Only minor fluctuations were observable in the Root Mean Square Fluctuation plots of chains A and B, having p-values of 0.38 and 0.15, respectively. These results depict that the complex is stable enough for a strong binding. The tropomyosin epitope of tilapia had three identified allergenic sequences, and findings indicate that the following species, common in the Philippines, have 100 percent similarity with all three protein sequences: mud crab, giant tiger prawn, blue swimming crab, Atlantic white shrimp, brown shrimp, and white leg shrimp. Other species, such as three spot swimming crab, Crucifix crab, and giant freshwater prawn can also be found in the Philippines but are not considered common, based on the PSA data from 2017 to 2019. The stated species are suggestive of being cross-reactive with the tropomyosin of Oreochromis mossambicus, meaning it is highly probable that a person allergic to tilapia could also be allergic to the listed species of seafood.
format text
author Endozo, Rikki Noreen S.
Kim, Abby Gayl A.
San Jose, Juan Miguel
author_facet Endozo, Rikki Noreen S.
Kim, Abby Gayl A.
San Jose, Juan Miguel
author_sort Endozo, Rikki Noreen S.
title An in silico approach on the allergenicity and cross reactivity of the tropomyosin epitope of Oreochromis mossambicus
title_short An in silico approach on the allergenicity and cross reactivity of the tropomyosin epitope of Oreochromis mossambicus
title_full An in silico approach on the allergenicity and cross reactivity of the tropomyosin epitope of Oreochromis mossambicus
title_fullStr An in silico approach on the allergenicity and cross reactivity of the tropomyosin epitope of Oreochromis mossambicus
title_full_unstemmed An in silico approach on the allergenicity and cross reactivity of the tropomyosin epitope of Oreochromis mossambicus
title_sort in silico approach on the allergenicity and cross reactivity of the tropomyosin epitope of oreochromis mossambicus
publisher Animo Repository
publishDate 2022
url https://animorepository.dlsu.edu.ph/etdb_physics/17
https://animorepository.dlsu.edu.ph/context/etdb_physics/article/1019/viewcontent/2022_SanJose_Endozo_Kim_An_in_silico_approach_on_the_allergenicity_Full_text.pdf
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