Difference between revisions of "Part:BBa K3610045"
 
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<partinfo>BBa_K3610045 short</partinfo>
 
<partinfo>BBa_K3610045 short</partinfo>
  
−
This part contains the ectodomain of the plant cell surface receptor EFR from A. thaliana fused to a yellow fluorescent protein. This part lacks the natural N-terminal signal sequence but instead uses the signal sequence from the alpha-Factor from yeast.
+
This part contains the ectodomain of the plant cell surface receptor EFR from <i>A. thaliana</i> fused to a yellow fluorescent protein. This part lacks the natural N-terminal signal sequence but instead uses the signal sequence from the alpha-Factor from yeast.
 +
 
 +
<html>
 +
</p>
 +
</html>
 +
__TOC__
  
 
===Usage and Biology===
 
===Usage and Biology===
 
====EFR====
 
====EFR====
−
Elongation factor-thermo unstable receptor (EFR) from A. thaliana is a plant pattern-recognition receptor (PRR). It is a cell surface receptor and part of the plants firts defence mechanism against potential pathogens. The EFR receptor is also a leucin-rich-repeats (LRR) receptor-like serine/threonine-protein kinase. The protein consists of an extracellular domain with leucin-rich repeats, a ligand binding domain found in many receptors, a single-pass transmembrane domain and finally an intracellular kinase domain. The ligand binding domain from EFR has high specificity to a bacterial pathogen-associated moleculat pattern (PAMP), namely the epitope elf18 of the abundant protein Elongation Factor Tu (EF-Tu), which is catalyzes the binding of aminoacyl-tRNA (aa-tRNA) to the ribosome in most prokaryotes and therefore is evolutionarily highly conserved. This makes the EFR a receptor that can be activated by the presence of a huge variety of bacteria. Upon binding of the ligand to the extracellular domain, the receptor dimerizes with its coreceptor BRI1-associated receptor kinase (BAK1). This interaction triggers the activation of the intracellular kinase domain of EFR and BAK1, initiating a signal cascade leading to an upregulation of immune response mechanisms.
+
Elongation factor-thermo unstable receptor (EFR) from <i>A. thaliana</i> is a plant pattern-recognition receptor (PRR). It is a cell surface receptor and part of the plants first defence mechanism against potential pathogens. The EFR receptor is also a leucine-rich-repeats (LRR) receptor-like serine/threonine-protein kinase. The protein consists of an extracellular domain with leucine-rich repeats, a ligand binding domain found in many receptors, a single-pass transmembrane domain and finally an intracellular kinase domain. The ligand binding domain from EFR has high specificity to a bacterial pathogen-associated moleculat pattern (PAMP), namely the epitope elf18 of the abundant protein Elongation Factor Tu (EF-Tu), which is catalyzes the binding of aminoacyl-tRNA (aa-tRNA) to the ribosome in most prokaryotes and therefore is evolutionarily highly conserved. This makes the EFR a receptor that can be activated by the presence of a huge variety of bacteria. Upon binding of the ligand to the extracellular domain, the receptor dimerizes with its coreceptor BRI1-associated receptor kinase (BAK1). This interaction triggers the activation of the intracellular kinase domain of EFR and BAK1, initiating a signal cascade leading to an upregulation of immune response mechanisms.
  
 
====EFR with YFP====
 
====EFR with YFP====
 
In this sequence, the C-terminal domain entailing the intracellular kinase domain was replaced with the sequence coding for the yellow fluorescent protein venus, while the ectodomain and the transmembrane domain, including the juxtamembrane domain were kept. Additionally, a signal sequence native to S. cerevisiae was fused to the N-terminal sequence, which does not contain the native signal peptide. This way, the protein can be integrated into the membrane during translation and the expression can be observed as with the receptor protein, the YFP (Exλ : 515 nm, Emλ : 528 nm) gets translated as well.
 
In this sequence, the C-terminal domain entailing the intracellular kinase domain was replaced with the sequence coding for the yellow fluorescent protein venus, while the ectodomain and the transmembrane domain, including the juxtamembrane domain were kept. Additionally, a signal sequence native to S. cerevisiae was fused to the N-terminal sequence, which does not contain the native signal peptide. This way, the protein can be integrated into the membrane during translation and the expression can be observed as with the receptor protein, the YFP (Exλ : 515 nm, Emλ : 528 nm) gets translated as well.
 +
 +
==Characterization==
 +
===Expression of EFR ectodomain/YFP in <i>S. cerevisiae</i>===
 +
In a first step we inserted the single fragments making up this part into a plasmid with a gentamycin-3-acetyltransferase gene and transformed <i>E. coli (DH10alpha)</i> with the plasmids for amplification. In the next step we assembled the fragments in a plasmid with a spectinomycin acetyltransferase and amplified the plasmids again in the same <i>E. coli</i> strain. For this step we applied the techniques of Golden Gate Cloning to get the fragments in the right order into the plasmid. The restriction enzyme we chose was BsaI. For expressing this part consisting of YFP and the receptor protein, we initially intended to use promoters of different strength to get more quantitative data. Finally, we got the construct in a plasmid with a truncated version of the ADH1 promoter from <i>S. cerevisiae</i>. For termination, this part has the terminator sequence of the enolase 2 protein from <i>S. cerevisiae</i>. The plasmid also contained the TRP1 gene, which encodes phosphoribosylanthranilate isomerase, an enzyme that catalyzes the third step in tryptophan biosynthesis. This enabled us to use the same plasmid for expression in <i>S. cerevisiae</i>. We prepared a medium containing YNB and free amino acids, without tryptophan. <i>S. cerevisiae</i> cells (AP4) were transfected with the plasmid and then plated on the selective medium.
 +
 +
====Microscopy====
 +
 +
After successful transformation of yeast cells we checked for enhanced fluorescence with confocal fluorescence microscopy. If expression of YFP (λEx = 515 nm, λEx = 528 nm) can clearly be observed, it is reasonable to assume that the receptor domain is expressed as well, as the YFP is fused to the receptor protein. Expression of the construct was confirmed. We failed, however, to confirm localization at the cell membrane.
 +
 +
[[File:T--UZurich--Control.png|800px|thumb|none|Figure 1: <i>S. cerevisiae</i> cells transformed with plasmids containing the EFR ectodomain fused to YFP. The results imply expression of the construct and also localization at the cell membrane.]]
 +
[[File:T--UZurich--eEFR.png|800px|thumb|none|Figure 2: Untransformed Control]]
 +
 +
Imaging of the <i>S. cerevisiae</i> cells, which had been previously transfected with plasmids containing this construct, revealed increased fluorescence levels than the untransfected control. These results imply increased expression of YFP, indicating expression of the EFR ectodomain.
 +
Additionally, the imaging results suggest that the proteins are in part localized at the cellular membrane, which is in alignment with our expectations as there is a secretion signal peptide and a transmembrane domain in the construct.<br>
 +
As localization at the cell membrane was something we were particularily interested in, we repeated the confocal microscopy step with an additional membrane stain. The cell membrane was stained with fm4-64, which fluoresces strongly after binding to the cell membrane ((λEX = 515nm and λEM = 640nm). The binding of the dye is happening rapidly and it is also reversible. If the time spent between staining and imaging is too long, then the dye will be taken up by the organism and stored in the vacuole. Imaging with a confocal microscope for YFP and the fm4-64 stain shows the spatial overlap of the red fluorescence of the stain and the yellow fluorescence of the protein fused to the receptors.
 +
[[File:T--UZurich--UT Membrane Stain.png|440px|thumb|left|Figure 3: Untransformed Control,(A) : YFP, (B) : FM4-64, (C): light field. (D): merge.Imaging of untransfected S. cerevisiae cells reveals hardly any fluorescence within the YFP spectrum]]<br>
 +
[[File:T--UZurich--eEFR Membrane Stain.png|450px|thumb|none|Figure 4: eEFR S. cerevisiae: (A) : YFP, (B) : FM4-64, (C) : light field. (D): merge. The construct eEFR:YFP is expressed and in about 25% of the cells clearly co-localized with the FM4-64 stain.]]
 +
 +
Confocal fluorescence microscopy with membrane staining confirmed what had been suggested previously with initial microscopy imaging. The results suggest that the receptor protein fused to the YFP gets epxpressed in <i>S. cerevisiae</i> and shows clear ring structures co-localized with the FM4-64 stain, indicating that there is localization at the plasma membrane.
 +
 +
====Spectrometry====
 +
 +
In addition to analyzing the cells with a microscope, we conducted a fluorescence assay with a plate reader. We conducted this experiment for multiple receptors at the same time. This way we were able to compare the expression levels of differnt versions of the BAK1 receptor.
 +
For each receptor we tried to isolate three different biological samples, however, not all cells grew.
 +
Ultimately, we only had two samples for the following <i>S. cerevisiae</i> cells: untransformed (Control), transformed with BAK1 ectodomain fused to YFP (eBAK) and the CORE ectodomain fused to YFP (eCORE).
 +
For the BAK1 with and without the native signal peptide fused to YFP (BAK+ and BAK-) and the EFR ectodomain fused to YFP (eEFR), we had samples from three different colonies.
 +
For each biological replicate, the optical density at absorbance of 600 nm (OD600) and the fluorescence levels were measured three times.
 +
 +
{| class="wikitable" width="95%"
 +
|-
 +
! scope="col", colspan ="10"| measured OD600 values (OD)
 +
|-
 +
! scope="col"|
 +
! scope="col", colspan="3"| Replicate 1
 +
! scope="col", colspan="3"| Replicate 2
 +
! scope="col", colspan="3"| Replicate 3
 +
|-
 +
! scope="row"| Blank
 +
|0,08200000226||0,08200000226||0,08389999717||||||||||||
 +
|-
 +
!Control
 +
|0,3806000054||0,3747999966||0,4221999943||0,1316999942||0,131400004||0,1176000014||||||
 +
|-
 +
!BAK+
 +
|0,4943000078||0,4638999999||0,4514000118||0,5781000257||0,5253999829||0,5799999833||0,2615999877||0,2171999961||0,2011999935
 +
|-
 +
!BAK-
 +
|1,417099953||1,365499973||1,368899941||0,6305999756||0,5633999705||0,6216999888||0,896600008||0,7882999778||0,8032000065
 +
|-
 +
!eBAK
 +
|1,009699941||0,8404999971||0,8934999704||0,2653000057||0,2368000001||0,2592999935||||||
 +
|-
 +
!eCORE
 +
|1,021499991||0,8616999984||0,9178000093||0,826300025||0,6888999939||0,7401999831||||||
 +
|-
 +
!eEFR
 +
|1,379699945||1,322700024||1,333500028||1,035899997||1,014000058||0,9526000023||0,4860999882||0,3797000051||0,3829999864
 +
|}
 +
 +
The following settings were applied for fluorescence measurements:
 +
 +
{|
 +
|Mode: ||Fluorescence Top Reading
 +
|-
 +
|Excitation Wavelength: ||485 nm
 +
|-
 +
|Emission Wavelength: ||535 nm
 +
|-
 +
|Excitation Bandwidth: ||20 nm
 +
|-
 +
|Emission Bandwidth: ||25 nm
 +
|-
 +
|Temperature: ||22.3°C
 +
|}
 +
 +
{| class="wikitable" width="95%"
 +
|-
 +
! scope="col", colspan ="10"| Fluorescence Top Reading (FTR)
 +
|-
 +
! scope="col"|
 +
! scope="col", colspan="3"| Replicate 1
 +
! scope="col", colspan="3"| Replicate 2
 +
! scope="col", colspan="3"| Replicate 3
 +
|-
 +
! scope="row"| Blank
 +
|1297||1282||1322||||||||||||
 +
|-
 +
!Control
 +
|2684||2474||2634||1852||1792||1750||||||
 +
|-
 +
!BAK+
 +
|3038||2813||2760||2836||2493||2788||2084||2072||2067
 +
|-
 +
!BAK-
 +
|35794||30319||31424||10792||9097||10517||22609||20227||21220
 +
|-
 +
!eBAK
 +
|26455||19828||21613||6614||5507||6229||||||
 +
|-
 +
!eCORE
 +
|10709||8382||9339||8957||7062||7735||||||
 +
|-
 +
!eEFR
 +
|43125||37782||39589||25641||24668||22517||12410||9054||9027
 +
|}
 +
 +
After measurement of the optical density and the fluorescence, the data were <i>blank corrected</i> (the average of the three blank measurements was subtracted from each measurement value).
 +
 +
The average of each of the three (or two) samples was calculated. From these values, the average was taken again.
 +
 +
After this step, we normalized the fluorescent output for OD600 (FTR/OD).
 +
The results of these calculations are displayed in the table below.
 +
{| class="wikitable"
 +
|-
 +
!Control
 +
!BAK+
 +
!BAK-
 +
!eBAK
 +
!eCORE
 +
!eEFR
 +
|-
 +
|4185,221063||9731,614266||26067,19254||28118,24739||3712,946478||23379,84399
 +
|}
 +
 +
If we set the values for the Control to 1 (Control = 1), then we get the fluorescence levels relative to the control, which is again diplayed in the table below.
 +
 +
{| class="wikitable"
 +
|-
 +
!Control
 +
!eCORE
 +
!eEFR
 +
!BAK-
 +
!BAK+
 +
!eBAK
 +
|-
 +
|1||0,8871565975||5,586286516||6,228390841||2,325233033||6,718461693
 +
|}
 +
 +
<br>
 +
[[File:T--UZurich--Spectrometer1.png|500px|none|left|Figure 5: Fluorescence values standardized for OD600 of the different receptors (C=Control). Cells with BAK+ showed only weak fluorescence, while BAK-, eBAK and eEFR showed a strong increase in the fluorescence levels. CORE did not display any increase when compared with untreated <i>S. cerevisiae</i> cells (autofluorescence).]]
 +
 +
Results of the plate reader suggested increased fluorescence through expression of YFP. The same was observed when cells were examined with the microscope. Therefore, <i>S. cerevisiae</i> cells express the plasmid containing the EFR ectodomain. Additionally, microscopy revealed localization at the cell membrane. This localization at the cell periphery is a big success as it shows, that the signal peptide from the alpha-Mating factor did, in fact induce translation into the membrane. Additionally, it was shown that the intracellular kinase domain is not necessary for membrane localization.
 +
 +
====Flow Cytometry====
 +
It has been important to us to examine a sample with different approaches simultaneously, which is why we were eager to also measure fluorescence intensity by flow cytometry. In a first phase, 100,000 cells were measured from each biological replicate (488/530 FITC channel in a BD FACSCanto II flow cytometer).
 +
In the next phase, the biological replicates for each construct were pooled together and 200,000 cells from each sample were measured.
 +
 +
[[File:T--UZurich--FACs.png|800px|thumb|none|Figure 6: Left: single biological replicates. right: pooled samples. With the exception of the construct with eCORE, cells transfected with our constructs showed considerably higher overall fluorescence intensities than the negative control.]]
 +
 +
Flow catometry provided further evidence for expression of the construct in <i>S. cerevisiae</i>. Cells transfected with plasmids containing eEFR showed significantly increased fluorescence intensities when examined as single biological replicates, as well as when the replicates were pooled together in one sample.
 +
 +
During our project, expression of the ectodomain of EFR fused to YFP was confirmed with three different approaches. We used a fluorometric plate reader, which suggested a strong increase in fluorescence intesity and we also got similar results when measuring fluorescence with flow cytometry. In addition to these results, fluorescence imaging also showed increased fluorescence and about 25% of the cells showed a very clear ring structure which co-localized with the memrbane stain FM4-64. These results suggest that the receptor ectodomain can get expressed in <i>S. cerevisiae</i> and it also gets localized at the cell periphery, although a lot of the proteins get stuck and are localized within the cell.
 +
 +
These results are very promising and open many doors to future applications of this plant PRR in synthetic biology as they strongly suggest that expression of this receptor ectodomain and membrane localization (with the alpha-Factor signal peptide) can be achieved.
 +
 +
This expression of the EFR ectodomain in <i> S. cerevisiae</i>, which is accompanied by localization at the cell membrane is a big achievement and we hope that many future teams can profit from our insights.
  
  

Latest revision as of 03:48, 28 October 2020


EFR ectodomain / YFP

This part contains the ectodomain of the plant cell surface receptor EFR from A. thaliana fused to a yellow fluorescent protein. This part lacks the natural N-terminal signal sequence but instead uses the signal sequence from the alpha-Factor from yeast.

Usage and Biology

EFR

Elongation factor-thermo unstable receptor (EFR) from A. thaliana is a plant pattern-recognition receptor (PRR). It is a cell surface receptor and part of the plants first defence mechanism against potential pathogens. The EFR receptor is also a leucine-rich-repeats (LRR) receptor-like serine/threonine-protein kinase. The protein consists of an extracellular domain with leucine-rich repeats, a ligand binding domain found in many receptors, a single-pass transmembrane domain and finally an intracellular kinase domain. The ligand binding domain from EFR has high specificity to a bacterial pathogen-associated moleculat pattern (PAMP), namely the epitope elf18 of the abundant protein Elongation Factor Tu (EF-Tu), which is catalyzes the binding of aminoacyl-tRNA (aa-tRNA) to the ribosome in most prokaryotes and therefore is evolutionarily highly conserved. This makes the EFR a receptor that can be activated by the presence of a huge variety of bacteria. Upon binding of the ligand to the extracellular domain, the receptor dimerizes with its coreceptor BRI1-associated receptor kinase (BAK1). This interaction triggers the activation of the intracellular kinase domain of EFR and BAK1, initiating a signal cascade leading to an upregulation of immune response mechanisms.

EFR with YFP

In this sequence, the C-terminal domain entailing the intracellular kinase domain was replaced with the sequence coding for the yellow fluorescent protein venus, while the ectodomain and the transmembrane domain, including the juxtamembrane domain were kept. Additionally, a signal sequence native to S. cerevisiae was fused to the N-terminal sequence, which does not contain the native signal peptide. This way, the protein can be integrated into the membrane during translation and the expression can be observed as with the receptor protein, the YFP (Exλ : 515 nm, Emλ : 528 nm) gets translated as well.

Characterization

Expression of EFR ectodomain/YFP in S. cerevisiae

In a first step we inserted the single fragments making up this part into a plasmid with a gentamycin-3-acetyltransferase gene and transformed E. coli (DH10alpha) with the plasmids for amplification. In the next step we assembled the fragments in a plasmid with a spectinomycin acetyltransferase and amplified the plasmids again in the same E. coli strain. For this step we applied the techniques of Golden Gate Cloning to get the fragments in the right order into the plasmid. The restriction enzyme we chose was BsaI. For expressing this part consisting of YFP and the receptor protein, we initially intended to use promoters of different strength to get more quantitative data. Finally, we got the construct in a plasmid with a truncated version of the ADH1 promoter from S. cerevisiae. For termination, this part has the terminator sequence of the enolase 2 protein from S. cerevisiae. The plasmid also contained the TRP1 gene, which encodes phosphoribosylanthranilate isomerase, an enzyme that catalyzes the third step in tryptophan biosynthesis. This enabled us to use the same plasmid for expression in S. cerevisiae. We prepared a medium containing YNB and free amino acids, without tryptophan. S. cerevisiae cells (AP4) were transfected with the plasmid and then plated on the selective medium.

Microscopy

After successful transformation of yeast cells we checked for enhanced fluorescence with confocal fluorescence microscopy. If expression of YFP (λEx = 515 nm, λEx = 528 nm) can clearly be observed, it is reasonable to assume that the receptor domain is expressed as well, as the YFP is fused to the receptor protein. Expression of the construct was confirmed. We failed, however, to confirm localization at the cell membrane.

Figure 1: S. cerevisiae cells transformed with plasmids containing the EFR ectodomain fused to YFP. The results imply expression of the construct and also localization at the cell membrane.
Figure 2: Untransformed Control

Imaging of the S. cerevisiae cells, which had been previously transfected with plasmids containing this construct, revealed increased fluorescence levels than the untransfected control. These results imply increased expression of YFP, indicating expression of the EFR ectodomain. Additionally, the imaging results suggest that the proteins are in part localized at the cellular membrane, which is in alignment with our expectations as there is a secretion signal peptide and a transmembrane domain in the construct.
As localization at the cell membrane was something we were particularily interested in, we repeated the confocal microscopy step with an additional membrane stain. The cell membrane was stained with fm4-64, which fluoresces strongly after binding to the cell membrane ((λEX = 515nm and λEM = 640nm). The binding of the dye is happening rapidly and it is also reversible. If the time spent between staining and imaging is too long, then the dye will be taken up by the organism and stored in the vacuole. Imaging with a confocal microscope for YFP and the fm4-64 stain shows the spatial overlap of the red fluorescence of the stain and the yellow fluorescence of the protein fused to the receptors.

Figure 3: Untransformed Control,(A) : YFP, (B) : FM4-64, (C): light field. (D): merge.Imaging of untransfected S. cerevisiae cells reveals hardly any fluorescence within the YFP spectrum

Figure 4: eEFR S. cerevisiae: (A) : YFP, (B) : FM4-64, (C) : light field. (D): merge. The construct eEFR:YFP is expressed and in about 25% of the cells clearly co-localized with the FM4-64 stain.

Confocal fluorescence microscopy with membrane staining confirmed what had been suggested previously with initial microscopy imaging. The results suggest that the receptor protein fused to the YFP gets epxpressed in S. cerevisiae and shows clear ring structures co-localized with the FM4-64 stain, indicating that there is localization at the plasma membrane.

Spectrometry

In addition to analyzing the cells with a microscope, we conducted a fluorescence assay with a plate reader. We conducted this experiment for multiple receptors at the same time. This way we were able to compare the expression levels of differnt versions of the BAK1 receptor. For each receptor we tried to isolate three different biological samples, however, not all cells grew. Ultimately, we only had two samples for the following S. cerevisiae cells: untransformed (Control), transformed with BAK1 ectodomain fused to YFP (eBAK) and the CORE ectodomain fused to YFP (eCORE). For the BAK1 with and without the native signal peptide fused to YFP (BAK+ and BAK-) and the EFR ectodomain fused to YFP (eEFR), we had samples from three different colonies. For each biological replicate, the optical density at absorbance of 600 nm (OD600) and the fluorescence levels were measured three times.

measured OD600 values (OD)
Replicate 1 Replicate 2 Replicate 3
Blank 0,08200000226 0,08200000226 0,08389999717
Control 0,3806000054 0,3747999966 0,4221999943 0,1316999942 0,131400004 0,1176000014
BAK+ 0,4943000078 0,4638999999 0,4514000118 0,5781000257 0,5253999829 0,5799999833 0,2615999877 0,2171999961 0,2011999935
BAK- 1,417099953 1,365499973 1,368899941 0,6305999756 0,5633999705 0,6216999888 0,896600008 0,7882999778 0,8032000065
eBAK 1,009699941 0,8404999971 0,8934999704 0,2653000057 0,2368000001 0,2592999935
eCORE 1,021499991 0,8616999984 0,9178000093 0,826300025 0,6888999939 0,7401999831
eEFR 1,379699945 1,322700024 1,333500028 1,035899997 1,014000058 0,9526000023 0,4860999882 0,3797000051 0,3829999864

The following settings were applied for fluorescence measurements:

Mode: Fluorescence Top Reading
Excitation Wavelength: 485 nm
Emission Wavelength: 535 nm
Excitation Bandwidth: 20 nm
Emission Bandwidth: 25 nm
Temperature: 22.3°C
Fluorescence Top Reading (FTR)
Replicate 1 Replicate 2 Replicate 3
Blank 1297 1282 1322
Control 2684 2474 2634 1852 1792 1750
BAK+ 3038 2813 2760 2836 2493 2788 2084 2072 2067
BAK- 35794 30319 31424 10792 9097 10517 22609 20227 21220
eBAK 26455 19828 21613 6614 5507 6229
eCORE 10709 8382 9339 8957 7062 7735
eEFR 43125 37782 39589 25641 24668 22517 12410 9054 9027

After measurement of the optical density and the fluorescence, the data were blank corrected (the average of the three blank measurements was subtracted from each measurement value).

The average of each of the three (or two) samples was calculated. From these values, the average was taken again.

After this step, we normalized the fluorescent output for OD600 (FTR/OD). The results of these calculations are displayed in the table below.

Control BAK+ BAK- eBAK eCORE eEFR
4185,221063 9731,614266 26067,19254 28118,24739 3712,946478 23379,84399

If we set the values for the Control to 1 (Control = 1), then we get the fluorescence levels relative to the control, which is again diplayed in the table below.

Control eCORE eEFR BAK- BAK+ eBAK
1 0,8871565975 5,586286516 6,228390841 2,325233033 6,718461693


Figure 5: Fluorescence values standardized for OD600 of the different receptors (C=Control). Cells with BAK+ showed only weak fluorescence, while BAK-, eBAK and eEFR showed a strong increase in the fluorescence levels. CORE did not display any increase when compared with untreated S. cerevisiae cells (autofluorescence).

Results of the plate reader suggested increased fluorescence through expression of YFP. The same was observed when cells were examined with the microscope. Therefore, S. cerevisiae cells express the plasmid containing the EFR ectodomain. Additionally, microscopy revealed localization at the cell membrane. This localization at the cell periphery is a big success as it shows, that the signal peptide from the alpha-Mating factor did, in fact induce translation into the membrane. Additionally, it was shown that the intracellular kinase domain is not necessary for membrane localization.

Flow Cytometry

It has been important to us to examine a sample with different approaches simultaneously, which is why we were eager to also measure fluorescence intensity by flow cytometry. In a first phase, 100,000 cells were measured from each biological replicate (488/530 FITC channel in a BD FACSCanto II flow cytometer). In the next phase, the biological replicates for each construct were pooled together and 200,000 cells from each sample were measured.

Figure 6: Left: single biological replicates. right: pooled samples. With the exception of the construct with eCORE, cells transfected with our constructs showed considerably higher overall fluorescence intensities than the negative control.

Flow catometry provided further evidence for expression of the construct in S. cerevisiae. Cells transfected with plasmids containing eEFR showed significantly increased fluorescence intensities when examined as single biological replicates, as well as when the replicates were pooled together in one sample.

During our project, expression of the ectodomain of EFR fused to YFP was confirmed with three different approaches. We used a fluorometric plate reader, which suggested a strong increase in fluorescence intesity and we also got similar results when measuring fluorescence with flow cytometry. In addition to these results, fluorescence imaging also showed increased fluorescence and about 25% of the cells showed a very clear ring structure which co-localized with the memrbane stain FM4-64. These results suggest that the receptor ectodomain can get expressed in S. cerevisiae and it also gets localized at the cell periphery, although a lot of the proteins get stuck and are localized within the cell.

These results are very promising and open many doors to future applications of this plant PRR in synthetic biology as they strongly suggest that expression of this receptor ectodomain and membrane localization (with the alpha-Factor signal peptide) can be achieved.

This expression of the EFR ectodomain in S. cerevisiae, which is accompanied by localization at the cell membrane is a big achievement and we hope that many future teams can profit from our insights.


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 355
    Illegal NheI site found at 1285
    Illegal NheI site found at 2203
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 1871
  • 1000
    COMPATIBLE WITH RFC[1000]