Revision as of 16:46, 1 October 2024

CMV-ATF2-mRuby2

Usage and Biology

ATF2 belongs to the mammalian ATF/CREB family (Kirsch et al., 2020) and gets phosphorylated by the antibiotic-detecting PknB-kinase (K5317013) of our sensor system. mRuby2 provides a fluorescent marker for visualization. In our cell-based & #946;-lactam ring-containing antibiotics sensor, ATF2 serves as a translator of changes in PknB activity at the level of gene regulation, in particular the activity of our engineered ATF2-3xCre2xAP1 promoter (K5317017).

Cloning

Theoretical Part Design

We placed the mRuby2 fluorescent marker (K5317001) downstream of ATF2 (K5317016), leading to a fusion of the reporter C-terminally. The CMV promoter, provided by the EGFP-C2 backbone (K3338020), enabels a constitutive expression of the fusionprotein in mammalian cells (Radhakrishnan et al., 2008).

Sequence and features

Cloning

The ATF2 insert was synthesized and the mRuby2 sequence amplifyed using the primers in table 1. The primers ensured approx. 20 bp-long overhangs at the 5' and 3' ends of the amplicons compatible with the backbone. We linearized EGFP-C2 with BamHI and AseI. The composite part-containing plasmid was assembled using the NEBBuilder® HIFI assembly kit, whereby the overhangs ensured the correct positioning of the insert in the backbone.

Table1: Primers used to extract the ATF2 gene sequence.

Figure 1: Assembled vector map with the ATF2 and mRuby2 inserts integrated into the pEGFP-C2 backbone, whereby mRuby2 is positioned downstream of ATF2, ensuring its C-terminally fusion to ATF2.

Characterisation

Transfection experiments in mammalian HEK293T cells assessed the functionality and sensitivity of ATF2. First, the composite part carrying plasmid was introduced via transfection to ensure the physiological localisation of ATF2 before co-transfecting experiments with the CMV-EGFP-PknB carrying plasmid (K5317018) and 3xCre3xAP1-miniCMV carrying plasmid (K5317022). The mRuby2 fluorescence signal was analyzed for localization by microscopy and quantifyed by FACS analysis.

Single-transfection experiments

To determine the basal expression and localization of ATF2 under unstimulated conditions, ATF2-mRuby2 expressing HEK293T cells were imaged without the presence of ampicillin.

Figure 2: Single-transfected HEK293T cells with the ATF2-mRuby2-C2 plasmid depicted under unstimulated conditions. Scale bar = 20 µm.

The correct expression of ATF2-mRuby2 was assumed, since the representative images in figure 2 show a moslty nuclear localization of the mRuby2 signal in HEK293T cells. The already primary nuclear localisation of ATF2 could be due to other mechanisms that activate ATF2 endogenously, since it is a mammalian transcription factor. Due to its physiological occurence in mammalian cells, we decided to use ATF2 as a crucial signal forwarding factor to mediate between the detecting PknB protein and the signal emitting 3xCre3xAP1-miniCMV promoter.

Co-transfection with PknB-EGFP

To test if PknB activation by the presence of beta-lactams lead to intracellular translocation of ATF2, we performed co-transfection experiments and exposed those HEK293T cells to ampicillin or remained them under unstimulated conditions.

Figure 3: The montage shows representative images of double-transfected CMV-PknB-EGFP and CMV-ATF2-mRuby2 HEK293T cells with and without ampicillin stimulation. Shown are brightfield (left), fluorescence channels for eGFP and mRuby2 and an overlay of the three channels with and without coloured signals (right). Scale bar = 100 µm.

The Co-transfection experiments showed that PknB and ATF2 do not inhibit each other's co-expression and that both are possibly interacting. Under ampicillin stimulating conditions, both signals increase slightly. This paring of kinase and transcription factor can be used for further experiments with the 3xCre3xAP1-miniCMV promoter to fully assemble the cell-based antibiotic sensor and test its responsiveness to beta-lactam exposure.

Triple-transfection experiments with EGFP-PknB and 3xCre3xAP1-miniCMV

The composite parts ATF2-mRuby2, EGFP-PknB (K5317018) and 3xCre3xAP1-miniCMV-miRFP670 (K5317022) integrated into backbone plasmids were co-transfected into HEK293T cells, with and without ampicillin supplementation of the media for four hours, to possibly detect changes in the miRFP670 signal. This provides information on whether our own promoter is recognised by the signal transmitter ATF2 after its activation by PknB with or without ampicillin present in the media. Therefore, providing neccessary information about the funtionality of our multi component sensor system.

Figure 4: Representative microscopy image of HEK293T cells expressing EGFP-PknB, ATF2-mRuby2 and 3xCre3xAP1-miniCMV-miRFP670. Shown are the fluorescence channels for EGFP, mRuby2 and miRFP670 (first three images from the left) and an overlay of the three channels (right). In a) is shown the basal activity of the promoter. In b) is shown the promoter activity after induction with 100 µg/mL ampicillin after four hours of incubation. Scale bar = 10 µm.

The representative HEK293T cells (Figure 4) co-transfected with our composite parts EGFP-PknB and ATF2-mRuby2, as well as our promoter-reporter construct 3xCre3xAP1-miniCMV-miRFP670 emitted signals in all three channels, indicating successful transfections. EGFP-PknB expression is shown in green, ATF2-mRuby2 expression in red, and the reporter miRFP670 expression in pink. Particularly noteworthy is again the correct localization of the prokaryotic membrane protein PknB in the eukaryotic cell membrane. To study whether the presence of beta-lactam antibiotics in the cell media will be sensed by PknB, leading to a phosphorylation of ATF2 and subsequently to an induction of our promoter-driven reporter fluorophore miRFP670, we incubated co-transfected HEK293T cells with ampicillin (100 µg/mL) for four hours. This led to a higher miRFP670 signal compared to unstimulated conditions. The detectable miRFFP670 signal even without the presence of ampicillin could be explained by possible binding of ATF2 to the 3xCre3xAP1-sites after its activation via other mammalian mechanisms, since ATF2 is a mmamalian transcription factor and possibly endogenously expressed and active. Nevertheless, the representative images of the miRFP670 channel indicate a increase in fluorescene intesity after ampicillin incubation suggesting a functional PASTA domain activity followed by ATF2 phosphorylation leading to miRFP670 expression.

References

Kirsch, K., Zeke, A., Tőke, O., Sok, P., Sethi, A., Sebő, A., Kumar, G. S., Egri, P., Póti, Á. L., Gooley, P., Peti, W., Bento, I., Alexa, A., & Reményi, A. (2020). Co-regulation of the transcription controlling ATF2 phosphoswitch by JNK and p38. Nature Communications, 11(1), 5769. https://doi.org/10.1038/s41467-020-19582-3

Radhakrishnan, P., Basma, H., Klinkebiel, D., Christman, J., & Cheng, P.-W. (2008). Cell type-specific activation of the cytomegalovirus promoter by dimethylsulfoxide and 5-Aza-2’-deoxycytidine. The International Journal of Biochemistry & Cell Biology, 40(9), 1944–1955. https://doi.org/10.1016/j.biocel.2008.02.014