glosensor tm camp reagent  (Promega)

Journal: Nature Communications

Article Title: Cryo-EM structure of an activated GPR4–Gs signaling complex

doi: 10.1038/s41467-025-55901-2

Figure Lengend Snippet: a , b The receptor–α5 interface in zGPR4 6.5 . Interacting residues are shown as sticks and are labeled. c , d Mutagenesis analysis of residues in zGPR4 ( c ) and hGPR4 ( d ) on the potency of G protein-coupling by the GloSensor cAMP assay. The maximum and minimum activation levels of WT GPR4 were set to 100 and 0%, respectively. The ΔpH 50 was calculated by dividing the potency (pH 50 ) of the mutant by the pH 50 of WT. Data are shown as means ± SEM from at least three independent experiments performed in triplicate. Source data are provided as a Source Data file.

Article Snippet: After incubating overnight, transfected cells were resuspended in DMEM added with 1% dialyzed FBS and then seeded into poly-l-lysine-coated 384-well plates (2 × 10 4 cells/well) (Costar, USA) for 9–24 h. After removing the culture medium, the cells were incubated with GloSensor TM cAMP reagent (Promega, USA) made in assay buffer (pH 8.4) for 1.5 h at 37 °C.

Techniques: Labeling, Mutagenesis, cAMP Assay, Activation Assay

Journal: Nature Communications

Article Title: Cryo-EM structure of an activated GPR4–Gs signaling complex

doi: 10.1038/s41467-025-55901-2

Figure Lengend Snippet: a – e Mutagenesis analysis of residues in zGPR4 on the proton potency by the GloSensor cAMP assay. Mutagenesis analysis of histidine residues in ECLs ( a ), highly conserved acidic residues in ECLs ( b ), partially conserved acidic residues ( c ), the Na coordinating residues ( d ), and the aromatic residues within the orthosteric pocket ( e ). The maximum and minimum activation levels of WT GPR4 were set to 100 and 0%, respectively. The ΔpH 50 was calculated by dividing the pH 50 of the mutant by the pH 50 of WT. Data are shown as means ± SEM from at least three independent experiments performed in triplicate. f Mapping the tested mutations on the zGPR4 structure. Mutations with positive effect (ΔpH 50 > 0.2 unit) are colored blue; mutations with negative effect (ΔpH 50 < −0.2 unit) are colored red; mutations with negligible effect (0.2 > ΔpH 50 > −0.2) are colored gray. Source data are provided as a Source Data file.

Article Snippet: After incubating overnight, transfected cells were resuspended in DMEM added with 1% dialyzed FBS and then seeded into poly-l-lysine-coated 384-well plates (2 × 10 4 cells/well) (Costar, USA) for 9–24 h. After removing the culture medium, the cells were incubated with GloSensor TM cAMP reagent (Promega, USA) made in assay buffer (pH 8.4) for 1.5 h at 37 °C.

Techniques: Mutagenesis, cAMP Assay, Activation Assay

Journal: Communications Biology

Article Title: Mechano-sensitivity of β2-adrenoceptors enhances constitutive activation of cAMP generation that is inhibited by inverse agonists

doi: 10.1038/s42003-024-06128-2

Figure Lengend Snippet: a The cubic ternary complex model for a GPCR interacting with agonists (A), inverse agonists (I) and Gs alpha subunits (Gs). In this model, the receptor can exist in two conformational states in the absence of ligands; an inactive R state and an active R* state that differ in their affinities for agonists, inverse agonists, and Gs alpha subunits. The conformational equilibrium that exists between R and R* (red arrows) explains the concept of constitutive receptor activity whereby basal activity can be observed in the absence of agonists in cells overexpressing native or constitutively active mutant β 2 ARs, as a consequence of binding to Gs proteins. b The mechanical mechanism for loading the multi-well plate into the PheraStar plate reader. The 96-well plate is placed on the mechanical plate stage and then automatically taken into the plate reader with a simple motor-driven linear movement. This process has the potential to provide a linear mechanical stimulation of the cell monolayer as the plate enters the light-tight reader. The initial entry of the plate into the reader is normally sufficient to activate the receptor. In most experiments, an initial read was taken at time zero and then the plate was immediately removed for the addition of ligands before re-entering the reader. In some experiments, the plate was added slowly manually to gain an initial GloSensor TM reading of basal levels. Created with Biorender.com.

Article Snippet: The cAMP GloSensor TM Human Embryonic Kidney 293 (HEK293G) cell line and GloSensor TM cAMP reagent were purchased from Promega (Madison, WI, USA).

Techniques: Activity Assay, Mutagenesis, Binding Assay

Journal: Communications Biology

Article Title: Mechano-sensitivity of β2-adrenoceptors enhances constitutive activation of cAMP generation that is inhibited by inverse agonists

doi: 10.1038/s42003-024-06128-2

Figure Lengend Snippet: Time-course of GloSensor TM luminescence stimulated by increasing concentrations of a isoprenaline and b salbutamol in a clonal HEK293G cell line overexpressing a transfected human TS-SNAP-β 2 AR. An initial luminescence read was made at time zero. The plate was then immediately removed from the PheraStar, agonists or HBSS added and the plate was then returned to the PheraStar and measurements continued every 1 min for 60 min. Values are mean ± SEM of 5 independent experiments. In each individual experiment, triplicate determinations were made. c Concentration–response curves of peak luminescence responses obtained for formoterol, isoprenaline, salmeterol and salbutamol in HEK293G cells overexpressing recombinant TS-SNAP-β 2 AR. Data are expressed as a percentage of the response to 1 nM isoprenaline (after normalisation of HBSS control response to zero) obtained in each individual experiment and represent mean ± SEM from five independent experiments ( n = 5). d A comparison of the time-course of GloSensor TM basal responses to HBSS addition in HEK293G cells overexpressing recombinant TS-SNAP-β 2 AR or wild-type (WT) HEK293G cells expressing endogenous β 2 ARs at very low levels. Values are mean ± SEM from five independent experiments. e , f Data from d showing the response in each cell line at t = 0 min prior to the addition of HBSS ( e ) and at the peak of the response to HBSS ( f ). ** p = 0.0079 (Mann–Whitney U test). At t = 0, there was no significant difference between the two cell lines ( p = 0.15; Mann–Whitney U test). Outlier analysis (both ROUT and Grubs method) confirmed that there were no significant outliers in the data sets. It should be noted that in these experiments, the zero time points were taken following initial plate loading and the plate was then immediately removed for the addition of an agonist or HBSS, and the plate was then reinserted into the plate reader.

Article Snippet: The cAMP GloSensor TM Human Embryonic Kidney 293 (HEK293G) cell line and GloSensor TM cAMP reagent were purchased from Promega (Madison, WI, USA).

Techniques: Transfection, Concentration Assay, Recombinant, Comparison, Expressing, MANN-WHITNEY

Journal: Communications Biology

Article Title: Mechano-sensitivity of β2-adrenoceptors enhances constitutive activation of cAMP generation that is inhibited by inverse agonists

doi: 10.1038/s42003-024-06128-2

Figure Lengend Snippet: Agonist E max , and log EC 50 determined for isoprenaline, formoterol, salbutamol and salmeterol from concentration–response curves obtained by cAMP GloSensor TM in HEK293G cells expressing endogenous β 2 ARs or HEK293G cells overexpressing recombinant TS-SNAP-β 2 AR

Article Snippet: The cAMP GloSensor TM Human Embryonic Kidney 293 (HEK293G) cell line and GloSensor TM cAMP reagent were purchased from Promega (Madison, WI, USA).

Techniques: Concentration Assay, Expressing, Recombinant

Journal: Communications Biology

Article Title: Mechano-sensitivity of β2-adrenoceptors enhances constitutive activation of cAMP generation that is inhibited by inverse agonists

doi: 10.1038/s42003-024-06128-2

Figure Lengend Snippet: Impact of mechanical stimulation on basal GloSensor TM time-course responses in a clonal HEK293G cell line overexpressing recombinant TS-SNAP-β 2 AR ( a , b ) or HEK293G cells endogenously expressing β 2 ARs ( c ). In all experiments, an initial luminescence read was made at time zero after initial plate entry into the PheraStar and before any additions. The plate was then immediately removed, HBSS or ICI-118551 added, and the plate was then returned to the PheraStar. Measurements were then made at 1 min and every min for 60 min in total. In a and c HBSS or ICI-118551 (1 μM) were added, and measurements of luminescence continued every minute from time = 1 min. a , c At 15, 30 and 45 min, the motorised stage of the PheraStar removed the plate from the instrument and then immediately returned it to the plate reader for further measurements every minute. In b no additions were made before measurements were made, although the motorised stage removed the plate and returned it to the PheraStar immediately after the time = 0 initial read to be consistent with the experiments in ( a ) and ( c ). At 30 min, the motorised stage of the PheraStar removed the plate from the instrument, HBSS or 1 μM ICI-118551 was added and the plate was then immediately returned to the plate reader for further measurements every min. In a – c values are mean ± SEM from five independent experiments. In each individual experiment, triplicate determinations were made.

Article Snippet: The cAMP GloSensor TM Human Embryonic Kidney 293 (HEK293G) cell line and GloSensor TM cAMP reagent were purchased from Promega (Madison, WI, USA).

Techniques: Recombinant, Expressing

Journal: Communications Biology

Article Title: Mechano-sensitivity of β2-adrenoceptors enhances constitutive activation of cAMP generation that is inhibited by inverse agonists

doi: 10.1038/s42003-024-06128-2

Figure Lengend Snippet: a , b Time-course of the basal GloSensor TM responses in HEK293G cells expressing HiBiT-D113A-β 2 AR, HEK293G cells expressing HiBiT-β 2 AR wild-type or native HEK293G cells with endogenous-β 2 ARs obtained in the absence ( a ) and presence ( b ) of 1 μM ICI-118551. In both ( a ) and ( b ), the plate was placed in the PheraStar at t = −15 min, the plate was then removed at time zero and HBSS or ICI-118551 (1 μM) was added, and the plate immediately returned to the PheraStar. Values are mean ± SEM from seven independent experiments. c Comparison of maximal basal peak responses obtained in HEK293G cells over-expressing HiBiT-D113A-β 2 AR, HEK293G cells over-expressing HiBiT-β 2 AR wild-type or in native HEK293G cells with endogenous expression of β 2 ARs. Values are mean ± SEM from seven independent experiments. * p < 0.05 or ** p < 0.01 (one-way ANOVA with Holm-Sidak multiple comparison test). HEK293G-HiBiT-D113A-β 2 AR versus HEK293G-HiBiT-D113A-β 2 AR in the presence of 1 μM ICI-118551 (not significant, p = 0.32); HEK293G-HiBiT-D113A-β 2 AR plus ICI-118551 versus endogenous HEK293G cells plus or minus ICI-118551 (both p = 0.035); HEK293G-HiBiT-D113A-β 2 AR plus 1 μM ICI-118551 versus wild-type β 2 AR ( p = 0.009). d Cell surface expression of HiBiT-D113A-β 2 AR in HEK293G cells. Receptor expression was monitored as reconstituted nanoluciferase luminescence following the addition of 0.2% purified LgBiT and 0.2% furimazine. Values are mean ± SEM from six independent experiments. * p < 0.05 or ** p < 0.01 (ANOVA with Tukey’s multiple comparison test for matched data). P = 0.045 and 0.005 for HiBiT-β 2 AR and HiBiT-D113A-β 2 AR, respectively relative to untransfected HEK293G cells. e Specific binding of ICI-118,551-βAla-βAla-BODIPY-X-630/650 (fluorescent ICI-118551) to HEK293G cells expressing wild-type HiBiT-β 2 AR or HiBiT-D113A-β 2 AR. Total and non-specific binding was determined following the re-complementation of full-length nanoluciferase with the addition of 0.2% purified LgBiT. Non-specific binding was determined in the presence of 50 μM ICI-118551. Specific binding was determined by subtraction of non-specific binding from the total binding at each concentration of fluorescent ICI-118551. Values are mean ± SEM from five independent experiments. f Specific binding determined with 100 nM fluorescent ICI-118551 in HEK293G cells expressing wild-type HiBiT-β 2 AR or HiBiT-D113A-β 2 AR. Data taken from ( e ) showing mean ± SEM and the individual means obtained in five separate experiments. **** p < 0.0001 (paired t -test).

Article Snippet: The cAMP GloSensor TM Human Embryonic Kidney 293 (HEK293G) cell line and GloSensor TM cAMP reagent were purchased from Promega (Madison, WI, USA).

Techniques: Expressing, Comparison, Purification, Binding Assay, Concentration Assay

Journal: Communications Biology

Article Title: Mechano-sensitivity of β2-adrenoceptors enhances constitutive activation of cAMP generation that is inhibited by inverse agonists

doi: 10.1038/s42003-024-06128-2

Figure Lengend Snippet: Cells were transiently transfected with the wild-type (WT) β 2 AR, a double mutant (N6A and N15A) β 2 AR or a triple mutant ((N6A, N15A, N178A) β 2 AR or a pcDNA3.1 control. Each β 2 AR construct contained an N-terminal HiBiT sequence. a Comparison of the cell surface expression of the three β 2 AR constructs. Receptor expression was monitored as reconstituted nanoluciferase luminescence following the addition of 0.2% purified LgBiT and 0.25% furimazine. Values are mean ± SEM from six independent experiments. There was no significant difference between the expression levels (one-way ANOVA with Tukey’s multiple comparison tests; p = 0.923, p = 0.252 and P = 0.427 for WT versus double mutant, WT versus triple mutant, and double mutant versus triple mutant, respectively). b Comparison of maximal peak responses to 1 μM isoprenaline produced by the three β 2 AR constructs. Values are mean ± SEM from six independent experiments. There was no significant difference between the maximal responses (one-way ANOVA with Tukey’s multiple comparisons test; p = 0.844, p = 0.946 and P = 0.663 for WT versus double mutant, WT versus triple mutant and double mutant versus triple mutant, respectively). c Time-course and d peak basal GloSensor TM responses in the presence and absence of 1 μM ICI-118551. An initial luminescence read was made at time zero. The plate was then immediately removed, HBSS or ICI-118551 added and then the plate was returned to the PheraStar. Measurements were then made at 1 min and every min for 60 min in total. Values are mean ± SEM from six independent experiments. **** p < 0.0001, ** p = 0.005; * p = 0.023 (two-way ANOVA with Tukey’s multiple comparison test). 1 μM ICI-118551 had no significant effect on the basal response to the triple mutant ( p = 0.595). e Time-course and f peak basal GloSensor TM responses in the presence and absence of 1 μM ICI-118551 or 1 μM isoprenaline f in HEK293 cells transfected with the triple β 2 AR mutant or pcDNA3.1. Values are mean ± SEM from six independent experiments. **** p < 0.0001 (two-way ANOVA with Sidak’s multiple comparisons test). The peak responses to isoprenaline were not significantly different ( p = 0.380). The peak responses to HBSS were also not significantly different ( p > 0.99). In both the triple mutant ( p > 0.77) and the pcDNA3.1 control cells ( p > 0.98), the inhibition by 1 μM ICI-118551 did not reach significance.

Article Snippet: The cAMP GloSensor TM Human Embryonic Kidney 293 (HEK293G) cell line and GloSensor TM cAMP reagent were purchased from Promega (Madison, WI, USA).

Techniques: Transfection, Mutagenesis, Construct, Sequencing, Comparison, Expressing, Purification, Produced, Inhibition

Journal: Cells

Article Title: Oxytocin Is a Positive Allosteric Modulator of κ-Opioid Receptors but Not δ-Opioid Receptors in the G Protein Signaling Pathway

doi: 10.3390/cells10102651

Figure Lengend Snippet: Effects of OT on inhibition of intracellular cAMP production induced by each KOR agonist in HEK293 cells stably coexpressing human KOR and Glosensor 22F protein. The cells were pretreated with 10 −6 M U50488 ( A ), 10 −6 dynorphin A ( B ), or 10 −5 M of morphine ( C ) in the absence and presence of 10 −6 M OT for 10 min and treated with forskolin (3 µM). The data are presented in terms of mean ± SEM values (( A ); n = 3, ( B ); n = 3, ( C ); n = 3). Two-way ANOVA was performed, followed by Bonferroni’s test, *** p < 0.001 compared to vehicle. # p < 0.05 and ## p < 0.01 compared to each agonist alone.

Article Snippet: Intracellular cAMP production was measured using the GloSensor TM cAMP assay (Promega) as described previously [ , ].

Techniques: Inhibition, Stable Transfection