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Improved genetically-encoded, FlincG-type fluorescent biosensors for neural cGMP imaging

Genetically-encoded biosensors are powerful tools for understanding cellular signal transduction mechanisms. In aiming to investigate cGMP signaling in neurones using the EGFP-based fluorescent biosensor, FlincG (fluorescent indicator for cGMP), we encountered weak or non-existent fluorescence after...

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Autores principales: Bhargava, Yogesh, Hampden-Smith, Kathryn, Chachlaki, Konstantina, Wood, Katherine C., Vernon, Jeffrey, Allerston, Charles K., Batchelor, Andrew M., Garthwaite, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3781335/
https://www.ncbi.nlm.nih.gov/pubmed/24068983
http://dx.doi.org/10.3389/fnmol.2013.00026
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author Bhargava, Yogesh
Hampden-Smith, Kathryn
Chachlaki, Konstantina
Wood, Katherine C.
Vernon, Jeffrey
Allerston, Charles K.
Batchelor, Andrew M.
Garthwaite, John
author_facet Bhargava, Yogesh
Hampden-Smith, Kathryn
Chachlaki, Konstantina
Wood, Katherine C.
Vernon, Jeffrey
Allerston, Charles K.
Batchelor, Andrew M.
Garthwaite, John
author_sort Bhargava, Yogesh
collection PubMed
description Genetically-encoded biosensors are powerful tools for understanding cellular signal transduction mechanisms. In aiming to investigate cGMP signaling in neurones using the EGFP-based fluorescent biosensor, FlincG (fluorescent indicator for cGMP), we encountered weak or non-existent fluorescence after attempted transfection with plasmid DNA, even in HEK293T cells. Adenoviral infection of HEK293T cells with FlincG, however, had previously proved successful. Both constructs were found to harbor a mutation in the EGFP domain and had a tail of 17 amino acids at the C-terminus that differed from the published sequence. These discrepancies were systematically examined, together with mutations found beneficial for the related GCaMP family of Ca(2+) biosensors, in a HEK293T cell line stably expressing both nitric oxide (NO)-activated guanylyl cyclase and phosphodiesterase-5. Restoring the mutated amino acid improved basal fluorescence whereas additional restoration of the correct C-terminal tail resulted in poor cGMP sensing as assessed by superfusion of either 8-bromo-cGMP or NO. Ultimately, two improved FlincGs were identified: one (FlincG2) had the divergent tail and gave moderate basal fluorescence and cGMP response amplitude and the other (FlincG3) had the correct tail, a GCaMP-like mutation in the EGFP region and an N-terminal tag, and was superior in both respects. All variants tested were strongly influenced by pH over the physiological range, in common with other EGFP-based biosensors. Purified FlincG3 protein exhibited a lower cGMP affinity (0.89 μM) than reported for the original FlincG (0.17 μM) but retained rapid kinetics and a 230-fold selectivity over cAMP. Successful expression of FlincG2 or FlincG3 in differentiated N1E-115 neuroblastoma cells and in primary cultures of hippocampal and dorsal root ganglion cells commends them for real-time imaging of cGMP dynamics in neural (and other) cells, and in their subcellular specializations.
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spelling pubmed-37813352013-09-25 Improved genetically-encoded, FlincG-type fluorescent biosensors for neural cGMP imaging Bhargava, Yogesh Hampden-Smith, Kathryn Chachlaki, Konstantina Wood, Katherine C. Vernon, Jeffrey Allerston, Charles K. Batchelor, Andrew M. Garthwaite, John Front Mol Neurosci Neuroscience Genetically-encoded biosensors are powerful tools for understanding cellular signal transduction mechanisms. In aiming to investigate cGMP signaling in neurones using the EGFP-based fluorescent biosensor, FlincG (fluorescent indicator for cGMP), we encountered weak or non-existent fluorescence after attempted transfection with plasmid DNA, even in HEK293T cells. Adenoviral infection of HEK293T cells with FlincG, however, had previously proved successful. Both constructs were found to harbor a mutation in the EGFP domain and had a tail of 17 amino acids at the C-terminus that differed from the published sequence. These discrepancies were systematically examined, together with mutations found beneficial for the related GCaMP family of Ca(2+) biosensors, in a HEK293T cell line stably expressing both nitric oxide (NO)-activated guanylyl cyclase and phosphodiesterase-5. Restoring the mutated amino acid improved basal fluorescence whereas additional restoration of the correct C-terminal tail resulted in poor cGMP sensing as assessed by superfusion of either 8-bromo-cGMP or NO. Ultimately, two improved FlincGs were identified: one (FlincG2) had the divergent tail and gave moderate basal fluorescence and cGMP response amplitude and the other (FlincG3) had the correct tail, a GCaMP-like mutation in the EGFP region and an N-terminal tag, and was superior in both respects. All variants tested were strongly influenced by pH over the physiological range, in common with other EGFP-based biosensors. Purified FlincG3 protein exhibited a lower cGMP affinity (0.89 μM) than reported for the original FlincG (0.17 μM) but retained rapid kinetics and a 230-fold selectivity over cAMP. Successful expression of FlincG2 or FlincG3 in differentiated N1E-115 neuroblastoma cells and in primary cultures of hippocampal and dorsal root ganglion cells commends them for real-time imaging of cGMP dynamics in neural (and other) cells, and in their subcellular specializations. Frontiers Media S.A. 2013-09-24 /pmc/articles/PMC3781335/ /pubmed/24068983 http://dx.doi.org/10.3389/fnmol.2013.00026 Text en Copyright © 2013 Bhargava, Hampden-Smith, Chachlaki, Wood, Vernon, Allerston, Batchelor and Garthwaite. http://creativecommons.org/licenses/by/3.0/ 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) or licensor 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 Neuroscience
Bhargava, Yogesh
Hampden-Smith, Kathryn
Chachlaki, Konstantina
Wood, Katherine C.
Vernon, Jeffrey
Allerston, Charles K.
Batchelor, Andrew M.
Garthwaite, John
Improved genetically-encoded, FlincG-type fluorescent biosensors for neural cGMP imaging
title Improved genetically-encoded, FlincG-type fluorescent biosensors for neural cGMP imaging
title_full Improved genetically-encoded, FlincG-type fluorescent biosensors for neural cGMP imaging
title_fullStr Improved genetically-encoded, FlincG-type fluorescent biosensors for neural cGMP imaging
title_full_unstemmed Improved genetically-encoded, FlincG-type fluorescent biosensors for neural cGMP imaging
title_short Improved genetically-encoded, FlincG-type fluorescent biosensors for neural cGMP imaging
title_sort improved genetically-encoded, flincg-type fluorescent biosensors for neural cgmp imaging
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3781335/
https://www.ncbi.nlm.nih.gov/pubmed/24068983
http://dx.doi.org/10.3389/fnmol.2013.00026
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