ShellPCR - Development of Elisa and Immuno-PCR for Sensitive and Specific Detection of Shellfish Tropomyosin

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ShellPCR - Development of Elisa and Immuno-PCR for Sensitive and Specific Detection of Shellfish Tropomyosin (en)
Authors

Publications

Optimization of extraction conditions of tropomyosin from razor mud shrimp and its quantification by developed ELISA

Radomirović, Mirjana; Čolaković, Maša; Pismestrović, Marina; Gligorijević, Nikola; Stanić-Vučinić, Dragana; Rajković, Andreja; Ćirković Veličković, Tanja

(Belgrade : Serbian Chemical Society, 2022)

TY  - CONF
AU  - Radomirović, Mirjana
AU  - Čolaković, Maša
AU  - Pismestrović, Marina
AU  - Gligorijević, Nikola
AU  - Stanić-Vučinić, Dragana
AU  - Rajković, Andreja
AU  - Ćirković Veličković, Tanja
PY  - 2022
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/6823
AB  - Tropomyosin (TPM) is considered as a major allergen among different shellfish species.
Therefore, the development of methods for quantifying TPM in food products iscrucial for
allergic persons. Several extraction buffers were tested for their efficiency in recovering
proteins from fresh frozen and cooked razor mud shrimp during 2 and 24 hours of
extraction. The protein content was quantified using the Bradford protein assay. SDSPAGE
was used for protein profiling of soluble extracts. Sandwich ELISA was developed
and used to quantify TPM content. None of the extraction buffers showed a significant
difference in total protein content between 2 and 24 hours of extraction. Significantly
fewer proteins were extracted from cooked shrimp compared to the raw shrimp. ELISA
quantification showed that phosphate-buffered saline (PBS) containing 1 M NaCl (PBSN)
and carbonate buffer, pH 10, extracted approximately 6 times higher amount of
tropomyosin in comparison to PBS, highlighting the importance of choosing the
appropriate extraction buffer for the precise quantification of TPM. Traditionally used
extraction buffer PBS could significantly underestimate shrimp TPM content.
AB  - Tropomiozin (TPM) se smatra glavnim alergenom morskih plodova. Razvoj metoda za kvantifikaciju TPM-a u prehrambenim proizvodima je ključan za alergične osobe. Nekoliko pufera za ekstrakciju je upoređeno u pogledu efikasnosti ekstrakcije protein iz sveže zamrznutih i kuvanih gambora, tokom 2 i 24 časa. Sadržaj proteina u solubilnim ekstraktima je određen Bredfordovom metodom. Proteinski profil ekstrakata je analiziran SDS-PAGE metodom. Za kvantifikaciju TPM-a je razvijena sendvič ELISA metoda. Nijedan puffer nije pokazao značajnu razliku u količini ekstrahovanih protein nakon 2 i 24 časa ekstrakcije. U poređenju sa sirovim, značajno manje proteina je ekstrahovano iz kuvanih gambora. Kvantifikacija TPM-a ELISA metodom je pokazala da se fosfatom puferisanim fiziološkim rastvorom (PBS) koji sadrži 1 M NaCl (PBSN) i karbonatnim 
puferom, pH 10, ekstrahuje oko 6 puta više TPM-a u poređenju sa PBS-om. Ovo ukazuje 
na značaj odabira adekvatnog pufera za ekstrakciju TPM-a, jer se upotrebom tradicionalno
korišćenih pufera može potceniti koncentracija TPM-a u gamborima.
PB  - Belgrade : Serbian Chemical Society
C3  - 58th Meeting of  the Serbian Chemical Society - Book of abstracts, Proceedings,  June 9-10, 2022 Belgrade / 58. Savetovanje Srpskog hemijskog društva, Kratki izvodi radova, Knjiga radova, 9. i 10. jun 2022. godine, Beograd
T1  - Optimization of extraction conditions of tropomyosin from razor mud  shrimp and its quantification by developed ELISA
SP  - 64
EP  - 64
UR  - https://hdl.handle.net/21.15107/rcub_cer_6823
ER  - 
@conference{
author = "Radomirović, Mirjana and Čolaković, Maša and Pismestrović, Marina and Gligorijević, Nikola and Stanić-Vučinić, Dragana and Rajković, Andreja and Ćirković Veličković, Tanja",
year = "2022",
abstract = "Tropomyosin (TPM) is considered as a major allergen among different shellfish species.
Therefore, the development of methods for quantifying TPM in food products iscrucial for
allergic persons. Several extraction buffers were tested for their efficiency in recovering
proteins from fresh frozen and cooked razor mud shrimp during 2 and 24 hours of
extraction. The protein content was quantified using the Bradford protein assay. SDSPAGE
was used for protein profiling of soluble extracts. Sandwich ELISA was developed
and used to quantify TPM content. None of the extraction buffers showed a significant
difference in total protein content between 2 and 24 hours of extraction. Significantly
fewer proteins were extracted from cooked shrimp compared to the raw shrimp. ELISA
quantification showed that phosphate-buffered saline (PBS) containing 1 M NaCl (PBSN)
and carbonate buffer, pH 10, extracted approximately 6 times higher amount of
tropomyosin in comparison to PBS, highlighting the importance of choosing the
appropriate extraction buffer for the precise quantification of TPM. Traditionally used
extraction buffer PBS could significantly underestimate shrimp TPM content., Tropomiozin (TPM) se smatra glavnim alergenom morskih plodova. Razvoj metoda za kvantifikaciju TPM-a u prehrambenim proizvodima je ključan za alergične osobe. Nekoliko pufera za ekstrakciju je upoređeno u pogledu efikasnosti ekstrakcije protein iz sveže zamrznutih i kuvanih gambora, tokom 2 i 24 časa. Sadržaj proteina u solubilnim ekstraktima je određen Bredfordovom metodom. Proteinski profil ekstrakata je analiziran SDS-PAGE metodom. Za kvantifikaciju TPM-a je razvijena sendvič ELISA metoda. Nijedan puffer nije pokazao značajnu razliku u količini ekstrahovanih protein nakon 2 i 24 časa ekstrakcije. U poređenju sa sirovim, značajno manje proteina je ekstrahovano iz kuvanih gambora. Kvantifikacija TPM-a ELISA metodom je pokazala da se fosfatom puferisanim fiziološkim rastvorom (PBS) koji sadrži 1 M NaCl (PBSN) i karbonatnim 
puferom, pH 10, ekstrahuje oko 6 puta više TPM-a u poređenju sa PBS-om. Ovo ukazuje 
na značaj odabira adekvatnog pufera za ekstrakciju TPM-a, jer se upotrebom tradicionalno
korišćenih pufera može potceniti koncentracija TPM-a u gamborima.",
publisher = "Belgrade : Serbian Chemical Society",
journal = "58th Meeting of  the Serbian Chemical Society - Book of abstracts, Proceedings,  June 9-10, 2022 Belgrade / 58. Savetovanje Srpskog hemijskog društva, Kratki izvodi radova, Knjiga radova, 9. i 10. jun 2022. godine, Beograd",
title = "Optimization of extraction conditions of tropomyosin from razor mud  shrimp and its quantification by developed ELISA",
pages = "64-64",
url = "https://hdl.handle.net/21.15107/rcub_cer_6823"
}
Radomirović, M., Čolaković, M., Pismestrović, M., Gligorijević, N., Stanić-Vučinić, D., Rajković, A.,& Ćirković Veličković, T.. (2022). Optimization of extraction conditions of tropomyosin from razor mud  shrimp and its quantification by developed ELISA. in 58th Meeting of  the Serbian Chemical Society - Book of abstracts, Proceedings,  June 9-10, 2022 Belgrade / 58. Savetovanje Srpskog hemijskog društva, Kratki izvodi radova, Knjiga radova, 9. i 10. jun 2022. godine, Beograd
Belgrade : Serbian Chemical Society., 64-64.
https://hdl.handle.net/21.15107/rcub_cer_6823
Radomirović M, Čolaković M, Pismestrović M, Gligorijević N, Stanić-Vučinić D, Rajković A, Ćirković Veličković T. Optimization of extraction conditions of tropomyosin from razor mud  shrimp and its quantification by developed ELISA. in 58th Meeting of  the Serbian Chemical Society - Book of abstracts, Proceedings,  June 9-10, 2022 Belgrade / 58. Savetovanje Srpskog hemijskog društva, Kratki izvodi radova, Knjiga radova, 9. i 10. jun 2022. godine, Beograd. 2022;:64-64.
https://hdl.handle.net/21.15107/rcub_cer_6823 .
Radomirović, Mirjana, Čolaković, Maša, Pismestrović, Marina, Gligorijević, Nikola, Stanić-Vučinić, Dragana, Rajković, Andreja, Ćirković Veličković, Tanja, "Optimization of extraction conditions of tropomyosin from razor mud  shrimp and its quantification by developed ELISA" in 58th Meeting of  the Serbian Chemical Society - Book of abstracts, Proceedings,  June 9-10, 2022 Belgrade / 58. Savetovanje Srpskog hemijskog društva, Kratki izvodi radova, Knjiga radova, 9. i 10. jun 2022. godine, Beograd (2022):64-64,
https://hdl.handle.net/21.15107/rcub_cer_6823 .

Extraction and quantification of tropomyosin in selected samples of shellfish

Radomirović, Mirjana; Gligorijević, Nikola; Stanić-Vučinić, Dragana; Rajković, Andreja; Ćirković Veličković, Tanja

(Sociedade Portuguesa de Química, 2021)

TY  - CONF
AU  - Radomirović, Mirjana
AU  - Gligorijević, Nikola
AU  - Stanić-Vučinić, Dragana
AU  - Rajković, Andreja
AU  - Ćirković Veličković, Tanja
PY  - 2021
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/7280
AB  - Food allergies affect up to 10% of the general population and represent an important health problem in the field of
food safety in industrialized countries. Hence, developing reliable, specific, and sensitive methods for detecting and
quantifying allergens in food products is of high importance. Shellfish have been recognized as one of the eight
most common sources of allergens, with tropomyosin (TPM) being considered a major heat-stable allergen, having
a highly conserved amino acid sequence among different shellfish species. Allergenicity of TPM may change during
food processing, such as cooking. The objective of this study was to develop an enzyme-linked immunosorbent
assay (ELISA) for the detection and quantification of shellfish tropomyosin in food samples.
Two different extraction buffers - phosphate-buffered saline (PBS) and PBS containing 1 M sodium-chloride
(PBSN), were compared for their ability to recover proteins from pre-cooked frozen Mediterranean mussel (Mytilus
galloprovincialis) and fresh frozen razor mud shrimp (Solenocera melantho). The samples were additionally cooked
according to the manufacturer's instruction and analyzed as such. The protein content was quantified using Bradford
protein assay, and the protein components of soluble extracts were profiled using SDS-PAGE. TPM presence was
confirmed using Western blot. Sandwich ELISA was developed using a monoclonal anti-TPM antibody as a capture
antibody, while polyclonal anti-TPM antibody served as a detection antibody and was coupled to the biotinylated
secondary antibody and streptavidin-alkaline phosphatase conjugate. Tropomyosin was quantified using highly
purified natural shrimp tropomyosin as standard.
The profile of extracted proteins was changed when using PBSN instead of PBS. A higher concentration of proteins
was recovered from raw shrimp using PBSN instead of PBS. At the same time, the type of extraction buffer did not
affect protein recovery either from heated shrimp or pre-cooked/heated mussels. Significantly fewer proteins were
extracted from cooked shrimp sample compared to the raw shrimp, while cooking showed no effect on the extraction
of proteins from mussels. Cooking did not affect TPM recognition in Western blot. TPM was quantified in shrimp
samples in sandwich ELISA. However, developed ELISA could not quantify mussel's TPM, indicating that this
approach may distinguish mussels and shrimp TPM.
PB  - Sociedade Portuguesa de Química
C3  - Book of Abstracts - XXI EuroFoodChem conference, 22nd-24th November, 2021, Virtual Congress
T1  - Extraction and quantification of tropomyosin in selected samples of shellfish
SP  - 118
EP  - 118
UR  - https://hdl.handle.net/21.15107/rcub_cer_7280
ER  - 
@conference{
author = "Radomirović, Mirjana and Gligorijević, Nikola and Stanić-Vučinić, Dragana and Rajković, Andreja and Ćirković Veličković, Tanja",
year = "2021",
abstract = "Food allergies affect up to 10% of the general population and represent an important health problem in the field of
food safety in industrialized countries. Hence, developing reliable, specific, and sensitive methods for detecting and
quantifying allergens in food products is of high importance. Shellfish have been recognized as one of the eight
most common sources of allergens, with tropomyosin (TPM) being considered a major heat-stable allergen, having
a highly conserved amino acid sequence among different shellfish species. Allergenicity of TPM may change during
food processing, such as cooking. The objective of this study was to develop an enzyme-linked immunosorbent
assay (ELISA) for the detection and quantification of shellfish tropomyosin in food samples.
Two different extraction buffers - phosphate-buffered saline (PBS) and PBS containing 1 M sodium-chloride
(PBSN), were compared for their ability to recover proteins from pre-cooked frozen Mediterranean mussel (Mytilus
galloprovincialis) and fresh frozen razor mud shrimp (Solenocera melantho). The samples were additionally cooked
according to the manufacturer's instruction and analyzed as such. The protein content was quantified using Bradford
protein assay, and the protein components of soluble extracts were profiled using SDS-PAGE. TPM presence was
confirmed using Western blot. Sandwich ELISA was developed using a monoclonal anti-TPM antibody as a capture
antibody, while polyclonal anti-TPM antibody served as a detection antibody and was coupled to the biotinylated
secondary antibody and streptavidin-alkaline phosphatase conjugate. Tropomyosin was quantified using highly
purified natural shrimp tropomyosin as standard.
The profile of extracted proteins was changed when using PBSN instead of PBS. A higher concentration of proteins
was recovered from raw shrimp using PBSN instead of PBS. At the same time, the type of extraction buffer did not
affect protein recovery either from heated shrimp or pre-cooked/heated mussels. Significantly fewer proteins were
extracted from cooked shrimp sample compared to the raw shrimp, while cooking showed no effect on the extraction
of proteins from mussels. Cooking did not affect TPM recognition in Western blot. TPM was quantified in shrimp
samples in sandwich ELISA. However, developed ELISA could not quantify mussel's TPM, indicating that this
approach may distinguish mussels and shrimp TPM.",
publisher = "Sociedade Portuguesa de Química",
journal = "Book of Abstracts - XXI EuroFoodChem conference, 22nd-24th November, 2021, Virtual Congress",
title = "Extraction and quantification of tropomyosin in selected samples of shellfish",
pages = "118-118",
url = "https://hdl.handle.net/21.15107/rcub_cer_7280"
}
Radomirović, M., Gligorijević, N., Stanić-Vučinić, D., Rajković, A.,& Ćirković Veličković, T.. (2021). Extraction and quantification of tropomyosin in selected samples of shellfish. in Book of Abstracts - XXI EuroFoodChem conference, 22nd-24th November, 2021, Virtual Congress
Sociedade Portuguesa de Química., 118-118.
https://hdl.handle.net/21.15107/rcub_cer_7280
Radomirović M, Gligorijević N, Stanić-Vučinić D, Rajković A, Ćirković Veličković T. Extraction and quantification of tropomyosin in selected samples of shellfish. in Book of Abstracts - XXI EuroFoodChem conference, 22nd-24th November, 2021, Virtual Congress. 2021;:118-118.
https://hdl.handle.net/21.15107/rcub_cer_7280 .
Radomirović, Mirjana, Gligorijević, Nikola, Stanić-Vučinić, Dragana, Rajković, Andreja, Ćirković Veličković, Tanja, "Extraction and quantification of tropomyosin in selected samples of shellfish" in Book of Abstracts - XXI EuroFoodChem conference, 22nd-24th November, 2021, Virtual Congress (2021):118-118,
https://hdl.handle.net/21.15107/rcub_cer_7280 .