Cargando…
A Fluorescence Resonance Energy Transfer-Based Analytical Tool for Nitrate Quantification in Living Cells
[Image: see text] Nitrate (NO(3)(–)) is a critical source of nitrogen (N) available to microorganisms and plants. Nitrate sensing activates signaling pathways in the plant system that impinges upon, developmental, molecular, metabolic, and physiological responses locally, and globally. To sustain, t...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7689916/ https://www.ncbi.nlm.nih.gov/pubmed/33251465 http://dx.doi.org/10.1021/acsomega.0c04868 |
_version_ | 1783613960306556928 |
---|---|
author | Fatima, Urooj Ameen, Fuad Soleja, Neha Khan, Parvez Almansob, Abobakr Ahmad, Altaf |
author_facet | Fatima, Urooj Ameen, Fuad Soleja, Neha Khan, Parvez Almansob, Abobakr Ahmad, Altaf |
author_sort | Fatima, Urooj |
collection | PubMed |
description | [Image: see text] Nitrate (NO(3)(–)) is a critical source of nitrogen (N) available to microorganisms and plants. Nitrate sensing activates signaling pathways in the plant system that impinges upon, developmental, molecular, metabolic, and physiological responses locally, and globally. To sustain, the high crop productivity and high nutritional value along with the sustainable environment, the study of rate-controlling steps of a metabolic network of N assimilation through fluxomics becomes an attractive strategy. To monitor the flux of nitrate, we developed a non-invasive genetically encoded fluorescence resonance energy transfer (FRET)-based tool named “FLIP-NT” that monitors the real-time uptake of nitrate in the living cells. The developed nanosensor is suitable for real-time monitoring of nitrate flux in living cells at subcellular compartments with high spatio-temporal resolution. The developed FLIP-NT nanosensor was not affected by the pH change and have specificity for nitrate with an affinity constant (K(d)) of ∼5 μM. A series of affinity mutants have also been generated to expand the physiological detection range of the sensor protein with varying K(d) values. It has been found that this sensor successfully detects the dynamics of nitrate fluctuations in bacteria and yeast, without the disruption of cellular organization. This FLIP-NT nanosensor could be a very important tool that will help us to advance the understanding of nitrate signaling. |
format | Online Article Text |
id | pubmed-7689916 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-76899162020-11-27 A Fluorescence Resonance Energy Transfer-Based Analytical Tool for Nitrate Quantification in Living Cells Fatima, Urooj Ameen, Fuad Soleja, Neha Khan, Parvez Almansob, Abobakr Ahmad, Altaf ACS Omega [Image: see text] Nitrate (NO(3)(–)) is a critical source of nitrogen (N) available to microorganisms and plants. Nitrate sensing activates signaling pathways in the plant system that impinges upon, developmental, molecular, metabolic, and physiological responses locally, and globally. To sustain, the high crop productivity and high nutritional value along with the sustainable environment, the study of rate-controlling steps of a metabolic network of N assimilation through fluxomics becomes an attractive strategy. To monitor the flux of nitrate, we developed a non-invasive genetically encoded fluorescence resonance energy transfer (FRET)-based tool named “FLIP-NT” that monitors the real-time uptake of nitrate in the living cells. The developed nanosensor is suitable for real-time monitoring of nitrate flux in living cells at subcellular compartments with high spatio-temporal resolution. The developed FLIP-NT nanosensor was not affected by the pH change and have specificity for nitrate with an affinity constant (K(d)) of ∼5 μM. A series of affinity mutants have also been generated to expand the physiological detection range of the sensor protein with varying K(d) values. It has been found that this sensor successfully detects the dynamics of nitrate fluctuations in bacteria and yeast, without the disruption of cellular organization. This FLIP-NT nanosensor could be a very important tool that will help us to advance the understanding of nitrate signaling. American Chemical Society 2020-11-12 /pmc/articles/PMC7689916/ /pubmed/33251465 http://dx.doi.org/10.1021/acsomega.0c04868 Text en © 2020 The Authors. Published by American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Fatima, Urooj Ameen, Fuad Soleja, Neha Khan, Parvez Almansob, Abobakr Ahmad, Altaf A Fluorescence Resonance Energy Transfer-Based Analytical Tool for Nitrate Quantification in Living Cells |
title | A Fluorescence Resonance Energy Transfer-Based Analytical
Tool for Nitrate Quantification in Living Cells |
title_full | A Fluorescence Resonance Energy Transfer-Based Analytical
Tool for Nitrate Quantification in Living Cells |
title_fullStr | A Fluorescence Resonance Energy Transfer-Based Analytical
Tool for Nitrate Quantification in Living Cells |
title_full_unstemmed | A Fluorescence Resonance Energy Transfer-Based Analytical
Tool for Nitrate Quantification in Living Cells |
title_short | A Fluorescence Resonance Energy Transfer-Based Analytical
Tool for Nitrate Quantification in Living Cells |
title_sort | fluorescence resonance energy transfer-based analytical
tool for nitrate quantification in living cells |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7689916/ https://www.ncbi.nlm.nih.gov/pubmed/33251465 http://dx.doi.org/10.1021/acsomega.0c04868 |
work_keys_str_mv | AT fatimaurooj afluorescenceresonanceenergytransferbasedanalyticaltoolfornitratequantificationinlivingcells AT ameenfuad afluorescenceresonanceenergytransferbasedanalyticaltoolfornitratequantificationinlivingcells AT solejaneha afluorescenceresonanceenergytransferbasedanalyticaltoolfornitratequantificationinlivingcells AT khanparvez afluorescenceresonanceenergytransferbasedanalyticaltoolfornitratequantificationinlivingcells AT almansobabobakr afluorescenceresonanceenergytransferbasedanalyticaltoolfornitratequantificationinlivingcells AT ahmadaltaf afluorescenceresonanceenergytransferbasedanalyticaltoolfornitratequantificationinlivingcells AT fatimaurooj fluorescenceresonanceenergytransferbasedanalyticaltoolfornitratequantificationinlivingcells AT ameenfuad fluorescenceresonanceenergytransferbasedanalyticaltoolfornitratequantificationinlivingcells AT solejaneha fluorescenceresonanceenergytransferbasedanalyticaltoolfornitratequantificationinlivingcells AT khanparvez fluorescenceresonanceenergytransferbasedanalyticaltoolfornitratequantificationinlivingcells AT almansobabobakr fluorescenceresonanceenergytransferbasedanalyticaltoolfornitratequantificationinlivingcells AT ahmadaltaf fluorescenceresonanceenergytransferbasedanalyticaltoolfornitratequantificationinlivingcells |