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Real time optical detection of gold in living cells through genetically-encoded probe
To study the efflux of gold (Au) in living cells, a genetically encoded fluorescence resonance energy transfer (FRET)-based sensor has been developed. The gold-sensing domain GolB from Salmonella typhimurium has been fused to the N- and C-termini of the FRET pair enhanced cyan fluorescent protein (E...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9380193/ https://www.ncbi.nlm.nih.gov/pubmed/36090423 http://dx.doi.org/10.1039/d2ra02574d |
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author | Nazir, Rahila Mohsin, Mohd Siddiqi, Tariq Omar |
author_facet | Nazir, Rahila Mohsin, Mohd Siddiqi, Tariq Omar |
author_sort | Nazir, Rahila |
collection | PubMed |
description | To study the efflux of gold (Au) in living cells, a genetically encoded fluorescence resonance energy transfer (FRET)-based sensor has been developed. The gold-sensing domain GolB from Salmonella typhimurium has been fused to the N- and C-termini of the FRET pair enhanced cyan fluorescent protein (ECFP) and Venus respectively. In living cells, this probe is highly selective and sensitive to gold and it can withstand changes in variable pH ranges. GolSeN-25, the most efficient sensor variant, binds gold with an affinity (K(d)) of 0.3 × 10(−6) M, covering gold concentrations of nM to μM, and can be used for non-invasive real-time in vivo gold measurement in living cells. A simple and sensitive FRET probe was designed for the detection of gold with high selectivity and can be applied to the analysis of real samples. |
format | Online Article Text |
id | pubmed-9380193 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-93801932022-09-08 Real time optical detection of gold in living cells through genetically-encoded probe Nazir, Rahila Mohsin, Mohd Siddiqi, Tariq Omar RSC Adv Chemistry To study the efflux of gold (Au) in living cells, a genetically encoded fluorescence resonance energy transfer (FRET)-based sensor has been developed. The gold-sensing domain GolB from Salmonella typhimurium has been fused to the N- and C-termini of the FRET pair enhanced cyan fluorescent protein (ECFP) and Venus respectively. In living cells, this probe is highly selective and sensitive to gold and it can withstand changes in variable pH ranges. GolSeN-25, the most efficient sensor variant, binds gold with an affinity (K(d)) of 0.3 × 10(−6) M, covering gold concentrations of nM to μM, and can be used for non-invasive real-time in vivo gold measurement in living cells. A simple and sensitive FRET probe was designed for the detection of gold with high selectivity and can be applied to the analysis of real samples. The Royal Society of Chemistry 2022-08-16 /pmc/articles/PMC9380193/ /pubmed/36090423 http://dx.doi.org/10.1039/d2ra02574d Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Nazir, Rahila Mohsin, Mohd Siddiqi, Tariq Omar Real time optical detection of gold in living cells through genetically-encoded probe |
title | Real time optical detection of gold in living cells through genetically-encoded probe |
title_full | Real time optical detection of gold in living cells through genetically-encoded probe |
title_fullStr | Real time optical detection of gold in living cells through genetically-encoded probe |
title_full_unstemmed | Real time optical detection of gold in living cells through genetically-encoded probe |
title_short | Real time optical detection of gold in living cells through genetically-encoded probe |
title_sort | real time optical detection of gold in living cells through genetically-encoded probe |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9380193/ https://www.ncbi.nlm.nih.gov/pubmed/36090423 http://dx.doi.org/10.1039/d2ra02574d |
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