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New Cationic fac-[Re(CO)(3)(deeb)B2](+) Complex, Where B2 Is a Benzimidazole Derivative, as a Potential New Luminescent Dye for Proteins Separated by SDS-PAGE

Sodium-dodecyl-sulfate polyacrylamide gel electrophoresis (SDS-PAGE) can be used to separate proteins based mainly on their size such as in denaturing gels. Different staining methods have been reported to observe proteins in the gel matrix, where the most used dyes are generally anionic. Anionic dy...

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Autores principales: Carreño, Alexander, Gacitúa, Manuel, Solis-Céspedes, Eduardo, Páez-Hernández, Dayán, Swords, Wesley B., Meyer, Gerald J., Preite, Marcelo D., Chávez, Ivonne, Vega, Andrés, Fuentes, Juan A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8027506/
https://www.ncbi.nlm.nih.gov/pubmed/33842435
http://dx.doi.org/10.3389/fchem.2021.647816
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author Carreño, Alexander
Gacitúa, Manuel
Solis-Céspedes, Eduardo
Páez-Hernández, Dayán
Swords, Wesley B.
Meyer, Gerald J.
Preite, Marcelo D.
Chávez, Ivonne
Vega, Andrés
Fuentes, Juan A.
author_facet Carreño, Alexander
Gacitúa, Manuel
Solis-Céspedes, Eduardo
Páez-Hernández, Dayán
Swords, Wesley B.
Meyer, Gerald J.
Preite, Marcelo D.
Chávez, Ivonne
Vega, Andrés
Fuentes, Juan A.
author_sort Carreño, Alexander
collection PubMed
description Sodium-dodecyl-sulfate polyacrylamide gel electrophoresis (SDS-PAGE) can be used to separate proteins based mainly on their size such as in denaturing gels. Different staining methods have been reported to observe proteins in the gel matrix, where the most used dyes are generally anionic. Anionic dyes allow for interactions with protonated amino acids, retaining the dye in the proteins. Fluorescent staining is an alternative technique considered to be sensitive, safe, and versatile. Some anionic complexes based on d(6) transition metals have been used for this purpose, where cationic dyes have been less explored in this context. In this work, we synthesized and characterized a new monocationic rhenium complex fac-[Re(CO)(3)(deeb)B2](+) (where deeb is 4,4′-bis(ethoxycarbonyl)-2,2′-bpy and B2 is 2,4-di-tert-butyl-6-(3H-imidazo[4,5-c]pyridine-2-yl)phenol). We carried out a structural characterization of this complex by MS(+), FTIR, (1)H NMR, D(2)O exchange, and HHCOSY. Moreover, we carried out UV-Vis, luminescence, and cyclic voltammetry experiments to understand the effect of ligands on the complex’s electronic structure. We also performed relativistic theoretical calculations using the B3LYP/TZ2P level of theory and R-TDDFT within a dielectric continuum model (COSMO) to better understand electronic transitions and optical properties. We finally assessed the potential of fac-[Re(CO)(3)(deeb)B2](+) (as well as the precursor fac-Re(CO)(3)(deeb)Br and the free ligand B2) to stain proteins separated by SDS-PAGE. We found that only fac-[Re(CO)(3)(deeb)B2](+) proved viable to be directly used as a luminescent dye for proteins, presumably due to its interaction with negatively charged residues in proteins and by weak interactions provided by B2. In addition, fac-[Re(CO)(3)(deeb)B2](+) seems to interact preferentially with proteins and not with the gel matrix despite the presence of sodium dodecyl sulfate (SDS). In future applications, these alternative cationic complexes might be used alone or in combination with more traditional anionic compounds to generate counterion dye stains to improve the process.
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spelling pubmed-80275062021-04-09 New Cationic fac-[Re(CO)(3)(deeb)B2](+) Complex, Where B2 Is a Benzimidazole Derivative, as a Potential New Luminescent Dye for Proteins Separated by SDS-PAGE Carreño, Alexander Gacitúa, Manuel Solis-Céspedes, Eduardo Páez-Hernández, Dayán Swords, Wesley B. Meyer, Gerald J. Preite, Marcelo D. Chávez, Ivonne Vega, Andrés Fuentes, Juan A. Front Chem Chemistry Sodium-dodecyl-sulfate polyacrylamide gel electrophoresis (SDS-PAGE) can be used to separate proteins based mainly on their size such as in denaturing gels. Different staining methods have been reported to observe proteins in the gel matrix, where the most used dyes are generally anionic. Anionic dyes allow for interactions with protonated amino acids, retaining the dye in the proteins. Fluorescent staining is an alternative technique considered to be sensitive, safe, and versatile. Some anionic complexes based on d(6) transition metals have been used for this purpose, where cationic dyes have been less explored in this context. In this work, we synthesized and characterized a new monocationic rhenium complex fac-[Re(CO)(3)(deeb)B2](+) (where deeb is 4,4′-bis(ethoxycarbonyl)-2,2′-bpy and B2 is 2,4-di-tert-butyl-6-(3H-imidazo[4,5-c]pyridine-2-yl)phenol). We carried out a structural characterization of this complex by MS(+), FTIR, (1)H NMR, D(2)O exchange, and HHCOSY. Moreover, we carried out UV-Vis, luminescence, and cyclic voltammetry experiments to understand the effect of ligands on the complex’s electronic structure. We also performed relativistic theoretical calculations using the B3LYP/TZ2P level of theory and R-TDDFT within a dielectric continuum model (COSMO) to better understand electronic transitions and optical properties. We finally assessed the potential of fac-[Re(CO)(3)(deeb)B2](+) (as well as the precursor fac-Re(CO)(3)(deeb)Br and the free ligand B2) to stain proteins separated by SDS-PAGE. We found that only fac-[Re(CO)(3)(deeb)B2](+) proved viable to be directly used as a luminescent dye for proteins, presumably due to its interaction with negatively charged residues in proteins and by weak interactions provided by B2. In addition, fac-[Re(CO)(3)(deeb)B2](+) seems to interact preferentially with proteins and not with the gel matrix despite the presence of sodium dodecyl sulfate (SDS). In future applications, these alternative cationic complexes might be used alone or in combination with more traditional anionic compounds to generate counterion dye stains to improve the process. Frontiers Media S.A. 2021-03-25 /pmc/articles/PMC8027506/ /pubmed/33842435 http://dx.doi.org/10.3389/fchem.2021.647816 Text en Copyright © 2021 Carreño, Gacitúa, Solis-Céspedes, Páez-Hernández, Swords, Meyer, Preite, Chávez, Vega and Fuentes. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Chemistry
Carreño, Alexander
Gacitúa, Manuel
Solis-Céspedes, Eduardo
Páez-Hernández, Dayán
Swords, Wesley B.
Meyer, Gerald J.
Preite, Marcelo D.
Chávez, Ivonne
Vega, Andrés
Fuentes, Juan A.
New Cationic fac-[Re(CO)(3)(deeb)B2](+) Complex, Where B2 Is a Benzimidazole Derivative, as a Potential New Luminescent Dye for Proteins Separated by SDS-PAGE
title New Cationic fac-[Re(CO)(3)(deeb)B2](+) Complex, Where B2 Is a Benzimidazole Derivative, as a Potential New Luminescent Dye for Proteins Separated by SDS-PAGE
title_full New Cationic fac-[Re(CO)(3)(deeb)B2](+) Complex, Where B2 Is a Benzimidazole Derivative, as a Potential New Luminescent Dye for Proteins Separated by SDS-PAGE
title_fullStr New Cationic fac-[Re(CO)(3)(deeb)B2](+) Complex, Where B2 Is a Benzimidazole Derivative, as a Potential New Luminescent Dye for Proteins Separated by SDS-PAGE
title_full_unstemmed New Cationic fac-[Re(CO)(3)(deeb)B2](+) Complex, Where B2 Is a Benzimidazole Derivative, as a Potential New Luminescent Dye for Proteins Separated by SDS-PAGE
title_short New Cationic fac-[Re(CO)(3)(deeb)B2](+) Complex, Where B2 Is a Benzimidazole Derivative, as a Potential New Luminescent Dye for Proteins Separated by SDS-PAGE
title_sort new cationic fac-[re(co)(3)(deeb)b2](+) complex, where b2 is a benzimidazole derivative, as a potential new luminescent dye for proteins separated by sds-page
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8027506/
https://www.ncbi.nlm.nih.gov/pubmed/33842435
http://dx.doi.org/10.3389/fchem.2021.647816
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