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Site-Specific Labeling of Proteins with Near-IR Heptamethine Cyanine Dyes

Convenient labeling of proteins is important for observing its function under physiological conditions. In tissues particularly, heptamethine cyanine dyes (Cy-7) are valuable because they absorb in the near-infrared (NIR) region (750–900 nm) where light penetration is maximal. In this work, we found...

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Detalles Bibliográficos
Autores principales: Lin, Chen-Ming, Usama, Syed Muhammad, Burgess, Kevin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6278338/
https://www.ncbi.nlm.nih.gov/pubmed/30405016
http://dx.doi.org/10.3390/molecules23112900
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author Lin, Chen-Ming
Usama, Syed Muhammad
Burgess, Kevin
author_facet Lin, Chen-Ming
Usama, Syed Muhammad
Burgess, Kevin
author_sort Lin, Chen-Ming
collection PubMed
description Convenient labeling of proteins is important for observing its function under physiological conditions. In tissues particularly, heptamethine cyanine dyes (Cy-7) are valuable because they absorb in the near-infrared (NIR) region (750–900 nm) where light penetration is maximal. In this work, we found Cy-7 dyes with a meso-Cl functionality covalently binding to proteins with free Cys residues under physiological conditions (aqueous environments, at near neutral pH, and 37 °C). It transpired that the meso-Cl of the dye was displaced by free thiols in protein, while nucleophilic side-chains from amino acids like Tyr, Lys, and Ser did not react. This finding shows a new possibility for convenient and selective labeling of proteins with NIR fluorescent probes.
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spelling pubmed-62783382018-12-13 Site-Specific Labeling of Proteins with Near-IR Heptamethine Cyanine Dyes Lin, Chen-Ming Usama, Syed Muhammad Burgess, Kevin Molecules Article Convenient labeling of proteins is important for observing its function under physiological conditions. In tissues particularly, heptamethine cyanine dyes (Cy-7) are valuable because they absorb in the near-infrared (NIR) region (750–900 nm) where light penetration is maximal. In this work, we found Cy-7 dyes with a meso-Cl functionality covalently binding to proteins with free Cys residues under physiological conditions (aqueous environments, at near neutral pH, and 37 °C). It transpired that the meso-Cl of the dye was displaced by free thiols in protein, while nucleophilic side-chains from amino acids like Tyr, Lys, and Ser did not react. This finding shows a new possibility for convenient and selective labeling of proteins with NIR fluorescent probes. MDPI 2018-11-07 /pmc/articles/PMC6278338/ /pubmed/30405016 http://dx.doi.org/10.3390/molecules23112900 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lin, Chen-Ming
Usama, Syed Muhammad
Burgess, Kevin
Site-Specific Labeling of Proteins with Near-IR Heptamethine Cyanine Dyes
title Site-Specific Labeling of Proteins with Near-IR Heptamethine Cyanine Dyes
title_full Site-Specific Labeling of Proteins with Near-IR Heptamethine Cyanine Dyes
title_fullStr Site-Specific Labeling of Proteins with Near-IR Heptamethine Cyanine Dyes
title_full_unstemmed Site-Specific Labeling of Proteins with Near-IR Heptamethine Cyanine Dyes
title_short Site-Specific Labeling of Proteins with Near-IR Heptamethine Cyanine Dyes
title_sort site-specific labeling of proteins with near-ir heptamethine cyanine dyes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6278338/
https://www.ncbi.nlm.nih.gov/pubmed/30405016
http://dx.doi.org/10.3390/molecules23112900
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