A novel synthetic approach to tyrosine dimers based on pterin photosensitization
Oxidative damage to proteins leads to a variety of modifications that are markers of pathogenesis. One of the most important modifications is the dityrosine (Tyr₂ ) cross-link, resulting from an oxidative covalent bond between two tyrosines (Tyr). An optimized methodology for preparation of pure Tyr...
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| Autores principales: | , , , , , , |
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| Formato: | Articulo Preprint |
| Lenguaje: | Inglés |
| Publicado: |
2017
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| Materias: | |
| Acceso en línea: | http://sedici.unlp.edu.ar/handle/10915/128209 |
| Aporte de: |
| id |
I19-R120-10915-128209 |
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| record_format |
dspace |
| institution |
Universidad Nacional de La Plata |
| institution_str |
I-19 |
| repository_str |
R-120 |
| collection |
SEDICI (UNLP) |
| language |
Inglés |
| topic |
Química Dityrosine Oxidation Cross-linking Pterin Photocatalyzed synthesis Photoinduced electron transfer |
| spellingShingle |
Química Dityrosine Oxidation Cross-linking Pterin Photocatalyzed synthesis Photoinduced electron transfer Reid, Lara Olivia Castaño, Carolina Dántola, María Laura Lhiaubet-Vallet, Virginie Miranda, Miguel A. Marin, M. Luisa Thomas, Andrés Héctor A novel synthetic approach to tyrosine dimers based on pterin photosensitization |
| topic_facet |
Química Dityrosine Oxidation Cross-linking Pterin Photocatalyzed synthesis Photoinduced electron transfer |
| description |
Oxidative damage to proteins leads to a variety of modifications that are markers of pathogenesis. One of the most important modifications is the dityrosine (Tyr₂ ) cross-link, resulting from an oxidative covalent bond between two tyrosines (Tyr). An optimized methodology for preparation of pure Tyr₂ is important to investigate in detail its physicochemical properties and reactivity. Pterin (Ptr), the parent and unsubstituted compound of oxidized pterins, is able to photosensitize the cross-linking of free tyrosine (Tyr) and tyrosine residues of peptides and proteins through a photoinduced electron transfer mechanism. We have optimized a simple, one-step photocatalyzed formation of Tyr₂ , using Ptr as photocatalyst. Our procedure is carried out in aqueous solutions under UV-A radiation for few minutes. The purification of Tyr₂ is performed by reverse-phase chromatography. The obtained highly pure solution is used to fully characterize the Tyr₂ (exact mass and ¹H, ¹H- ¹H COSY; DEPT; HSQC and HMBC NMR experiments) and to deeper study its fluorescence properties. |
| format |
Articulo Preprint |
| author |
Reid, Lara Olivia Castaño, Carolina Dántola, María Laura Lhiaubet-Vallet, Virginie Miranda, Miguel A. Marin, M. Luisa Thomas, Andrés Héctor |
| author_facet |
Reid, Lara Olivia Castaño, Carolina Dántola, María Laura Lhiaubet-Vallet, Virginie Miranda, Miguel A. Marin, M. Luisa Thomas, Andrés Héctor |
| author_sort |
Reid, Lara Olivia |
| title |
A novel synthetic approach to tyrosine dimers based on pterin photosensitization |
| title_short |
A novel synthetic approach to tyrosine dimers based on pterin photosensitization |
| title_full |
A novel synthetic approach to tyrosine dimers based on pterin photosensitization |
| title_fullStr |
A novel synthetic approach to tyrosine dimers based on pterin photosensitization |
| title_full_unstemmed |
A novel synthetic approach to tyrosine dimers based on pterin photosensitization |
| title_sort |
novel synthetic approach to tyrosine dimers based on pterin photosensitization |
| publishDate |
2017 |
| url |
http://sedici.unlp.edu.ar/handle/10915/128209 |
| work_keys_str_mv |
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