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Serotonin G Protein-Coupled Receptor-Based Biosensing Modalities in Yeast

[Image: see text] Serotonin is a key neurotransmitter involved in numerous physiological processes and serves as an important precursor for manufacturing bioactive indoleamines and alkaloids used in the treatment of human pathologies. In humans, serotonin sensing and signaling can occur by 12 G prot...

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Autores principales: Lengger, Bettina, Hoch-Schneider, Emma E., Jensen, Christina N., Jakočiu̅nas, Tadas, Petersen, Anja A., Frimurer, Thomas M., Jensen, Emil D., Jensen, Michael K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9150182/
https://www.ncbi.nlm.nih.gov/pubmed/35452231
http://dx.doi.org/10.1021/acssensors.1c02061
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author Lengger, Bettina
Hoch-Schneider, Emma E.
Jensen, Christina N.
Jakočiu̅nas, Tadas
Petersen, Anja A.
Frimurer, Thomas M.
Jensen, Emil D.
Jensen, Michael K.
author_facet Lengger, Bettina
Hoch-Schneider, Emma E.
Jensen, Christina N.
Jakočiu̅nas, Tadas
Petersen, Anja A.
Frimurer, Thomas M.
Jensen, Emil D.
Jensen, Michael K.
author_sort Lengger, Bettina
collection PubMed
description [Image: see text] Serotonin is a key neurotransmitter involved in numerous physiological processes and serves as an important precursor for manufacturing bioactive indoleamines and alkaloids used in the treatment of human pathologies. In humans, serotonin sensing and signaling can occur by 12 G protein-coupled receptors (GPCRs) coupled to Gα proteins. In yeast, human serotonin GPCRs coupled to Gα proteins have previously been shown to function as whole-cell biosensors of serotonin. However, systematic characterization of serotonin biosensing modalities between variant serotonin GPCRs and application thereof for high-resolution serotonin quantification is still awaiting. To systematically assess GPCR signaling in response to serotonin, we characterized reporter gene expression at two different pHs of a 144-sized library encoding all 12 human serotonin GPCRs in combination with 12 different Gα proteins engineered in yeast. From this screen, we observed changes in the biosensor sensitivities of >4 orders of magnitude. Furthermore, adopting optimal biosensing designs and pH conditions enabled high-resolution high-performance liquid chromatography-validated sensing of serotonin produced in yeast. Lastly, we used the yeast platform to characterize 19 serotonin GPCR polymorphisms found in human populations. While major differences in signaling were observed among the individual polymorphisms when studied in yeast, a cross-comparison of selected variants in mammalian cells showed both similar and disparate results. Taken together, our study highlights serotonin biosensing modalities of relevance to both biotechnological and potential human health applications.
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spelling pubmed-91501822022-05-31 Serotonin G Protein-Coupled Receptor-Based Biosensing Modalities in Yeast Lengger, Bettina Hoch-Schneider, Emma E. Jensen, Christina N. Jakočiu̅nas, Tadas Petersen, Anja A. Frimurer, Thomas M. Jensen, Emil D. Jensen, Michael K. ACS Sens [Image: see text] Serotonin is a key neurotransmitter involved in numerous physiological processes and serves as an important precursor for manufacturing bioactive indoleamines and alkaloids used in the treatment of human pathologies. In humans, serotonin sensing and signaling can occur by 12 G protein-coupled receptors (GPCRs) coupled to Gα proteins. In yeast, human serotonin GPCRs coupled to Gα proteins have previously been shown to function as whole-cell biosensors of serotonin. However, systematic characterization of serotonin biosensing modalities between variant serotonin GPCRs and application thereof for high-resolution serotonin quantification is still awaiting. To systematically assess GPCR signaling in response to serotonin, we characterized reporter gene expression at two different pHs of a 144-sized library encoding all 12 human serotonin GPCRs in combination with 12 different Gα proteins engineered in yeast. From this screen, we observed changes in the biosensor sensitivities of >4 orders of magnitude. Furthermore, adopting optimal biosensing designs and pH conditions enabled high-resolution high-performance liquid chromatography-validated sensing of serotonin produced in yeast. Lastly, we used the yeast platform to characterize 19 serotonin GPCR polymorphisms found in human populations. While major differences in signaling were observed among the individual polymorphisms when studied in yeast, a cross-comparison of selected variants in mammalian cells showed both similar and disparate results. Taken together, our study highlights serotonin biosensing modalities of relevance to both biotechnological and potential human health applications. American Chemical Society 2022-04-22 2022-05-27 /pmc/articles/PMC9150182/ /pubmed/35452231 http://dx.doi.org/10.1021/acssensors.1c02061 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Lengger, Bettina
Hoch-Schneider, Emma E.
Jensen, Christina N.
Jakočiu̅nas, Tadas
Petersen, Anja A.
Frimurer, Thomas M.
Jensen, Emil D.
Jensen, Michael K.
Serotonin G Protein-Coupled Receptor-Based Biosensing Modalities in Yeast
title Serotonin G Protein-Coupled Receptor-Based Biosensing Modalities in Yeast
title_full Serotonin G Protein-Coupled Receptor-Based Biosensing Modalities in Yeast
title_fullStr Serotonin G Protein-Coupled Receptor-Based Biosensing Modalities in Yeast
title_full_unstemmed Serotonin G Protein-Coupled Receptor-Based Biosensing Modalities in Yeast
title_short Serotonin G Protein-Coupled Receptor-Based Biosensing Modalities in Yeast
title_sort serotonin g protein-coupled receptor-based biosensing modalities in yeast
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9150182/
https://www.ncbi.nlm.nih.gov/pubmed/35452231
http://dx.doi.org/10.1021/acssensors.1c02061
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