Difference between revisions of "Part:BBa K4035007"

Latest revision as of 00:57, 22 October 2021

Dimerization of the copper metallothionein 1 : CUP1-GGGGSEAAAKGGGGS-CUP1

This protein is made of two copies of the yeast copper metallothionein protein, CUP1 (BBa_M45090), linked together by a semi-rigid linker made of the GGGGSEAAAKGGGGS amino acid sequence.

Usage and Biology

Copper metallothionein CUP1 (BBa_M45090) is a protein responsible for copper binding in the yeast Saccharomyces cerevisiae. In order to increase the copper retrieval efficiency, two copies of CUP1 have been linked together by the GGGGSEAAAKGGGGS aa sequence. This linker is composed of two flexible regions GGGGS separated by a rigid region EAAAK, making the linker rigid in the center with 2 flexible arms attached to the CUP1 proteins. This allows to maintain a net distance between the two proteins, avoiding their interaction and incorrect folding, and at the same time allowing several degrees of freedom and preserving the correct biological activity. This fusion protein was expressed on the outer membrane of S. cerevisiae by insertion of this part sequence into the pCTcon2-V5 plasmid (1). The expression system (BBa_K4035014) consists of fusing the dimer on a yeast surface display (1) under the control of the Gal1 promoter. This results in the production of a fusion protein Aga2-CUP1-GGGGSEAAAKGGGGS-CUP1-V5.

Sequence and Features

Assembly Compatibility:

10
COMPATIBLE WITH RFC[10]
12
COMPATIBLE WITH RFC[12]
21
INCOMPATIBLE WITH RFC[21]
Illegal BamHI site found at 190
23
COMPATIBLE WITH RFC[23]
25
COMPATIBLE WITH RFC[25]
1000
COMPATIBLE WITH RFC[1000]

Characterization

Expression of the protein in S.cerevisiae

Western Blot Analysis

Figure 1 : V5 tagged CUP1 dimer expression in the yeast S.cerevisiae

In order to characterize the protein expression, two experiments were performed, the first being a Western Blot analysis. After having transformed the EBY100 yeast with our newly formed plasmid pCTcon2-dimer-V5, we analyzed its protein expression. For control we also tested the wild type yeast (untransformed) as well as a transformed yeast with the plasmid backbone (without insert) in SGCAA, a medium containing galactose allowing for protein expression through the activation of the Gal1 promoter. As the plasmid contains a Gal1 promoter, the system can only be expressed in the presence of galactose.

Figure 1 : The first lane (E2) is the yeast transformed with our plasmid containing the CUP1 dimer and the second and third lanes are, respectively, plasmid backbone and wild type yeast. EBY100 is the wild type yeast and serves as a negative control whereas pCTcon2-V5 is the transformed yeast with only the plasmid backbone and serves as a positive control.

Wild type yeast shows no presence of the V5 tag, as expected, while plasmid backbone has signal which proves that our system is expressed in the transformed yeast when induced with galactose. Our transformed yeast with the Aga2-CUP1-linker-CUP1-V5 protein also shows expression of the system.

We can see that we have two bands on the gel, one is approximately 30 kDa which is the size of the fusion protein Aga2-CUP1-linker-CUP1-V5 and the other is slightly smaller. The smaller band could be a truncated version of the protein since we identified a second in-frame start codon in the DNA sequence.

The presence of our CUP1 dimer in our yeast transformants is thus shown.

Immunocytochemistry Assay

Figure 2a : V5 tagged CUP1 dimer membrane expression in the yeast S.cerevisiae

To show that the fusion protein is expressed at the membrane of the cell we performed an Immunocytochemistry assay. The cells were incubated with a primary mouse anti-V5 antibody as well as with a secondary goat anti-mouse couple with Alexa Fluor 488. The same strains for control have been used namely, plasmid backbone induced (Figure 2c) and wild type yeast (Figure 2d).

The nuclei have been stained with DAPI and are depicted in blue on the figures. The green disks are representing the transformed yeast cells expressing the CUP1 dimer at their surface (Figure 2a).

Due to the more intense circle we can clearly see that our system is expressed on the membrane of the protein (better seen on Figure 2b which is a higher magnification picture of yeast transformed with a single copy of CUP1, part BBa_K4035001).

We can also remark that not all the cells are expressing the system. This is because the expression is not 100% efficient, concordant to the published expression system (1).

On the negative control, the little green signal we see is background noise or nonspecific antibody binding.

Figure 2b : V5 tagged CUP1 membrane expression in the yeast S.cerevisiae (BBa_K4035001), 488 nm excitation channel, 40x magnification

Figure 2c : EBY100, negative control

Figure 2d : V5 tag membrane expression in the yeast S.cerevisiae

@@ Line 3: / Line 3: @@
 <partinfo>BBa_K4035007 short</partinfo>
-This protein is made of two yeast copper metallotionein protein, CUP1 ([https://parts.igem.org/Part:BBa_M45090 BBa_M45090]), linked together by a semi-rigid linker made of the GGGGSEAAAKGGGGS amino acid sequence.
+This protein is made of two copies of the yeast copper metallothionein protein, CUP1 ([https://parts.igem.org/Part:BBa_M45090 BBa_M45090]), linked together by a semi-rigid linker made of the GGGGSEAAAKGGGGS amino acid sequence.
 ==Usage and Biology==
-Copper metallotionein CUP1 ([https://parts.igem.org/Part:BBa_M45090 BBa_M45090]) is a protein responsible for copper binding protein in the yeast Saccharomyces cerevisiae. In order to increase the copper retrieval efficiency, two copies of CUP1 were linked together and expressed at the outter surface of S. cerevisiae ([https://parts.igem.org/Part:BBa_K4035014 BBa_K4035014]). The linker is composed of two flexible regions GGGGS separated by a rigid region EAAAK, making the linker rigid in the center with 2 flexible arms attached to the CUP1 proteins.
+Copper metallothionein CUP1 ([https://parts.igem.org/Part:BBa_M45090 BBa_M45090]) is a protein responsible for copper binding in the yeast Saccharomyces cerevisiae. In order to increase the copper retrieval efficiency, two copies of CUP1 have been linked together by the GGGGSEAAAKGGGGS aa sequence. This linker is composed of two flexible regions GGGGS separated by a rigid region EAAAK, making the linker rigid in the center with 2 flexible arms attached to the CUP1 proteins. This allows to maintain a net distance between the two proteins, avoiding their interaction and incorrect folding, and at the same time allowing several degrees of freedom and preserving the correct biological activity. This fusion protein was expressed on the outer membrane of S. cerevisiae by insertion of this part sequence into the pCTcon2-V5 plasmid (1). The expression system ([https://parts.igem.org/Part:BBa_K4035014 BBa_K4035014]) consists of fusing the dimer on a yeast surface display (1) under the control of the Gal1 promoter. This results in the production of a fusion protein Aga2-CUP1-GGGGSEAAAKGGGGS-CUP1-V5.
 ==Sequence and Features==
 <partinfo>BBa_K4035007 SequenceAndFeatures</partinfo>
-==Characterization==
-===Expression of the protein in the recombinant yeast===
-'''Western Blot Analysis'''
-[[File:BBa_K4035001_WEB_image_1.jpg|400px|thumb|right|'''Figure 1''' : Western Blot results]]
-The protein expression characterization has been accomplish by two experiments, the first being a Western Blot analysis. After having transformed the EBY100 yeast with our newly formed plasmid pCTcon2V5-CUP1-GGGGSEAAAKGGGGS-CUP1-V5 we tested its protein expression. For control we also tested the wild type yeast (untransformed) as well as a transformed yeast with the plasmid backbone (without insert) in two different media, one containing galactose and allowing expression and the other, lacking galactose and thus blocking expression of the protein. As the plasmid contains a Gal1 promoter, the system can only be expressed in the presence of galactose.
-'''Figure 1''' : The first two lines, EBY100 and pCTcon2V5 without galactose which are, respectively, wild type yeast and uninduced transformed yeast with the backbone plasmid, serve as negative controls, and show no presence of the V5 tag, as we expected.  The third line, pCTcon2V5 + galactose is the induced transformed yeast with the backbone plasmid and shows expression of the V5 tag which proves that our system is expressed in the transformed yeast when induced with galactose. The fourth line is our transformed yeast with the recombinant plasmid pCTcon2-CUP1-GGGGSEAAAKGGGGS-CUP1-V5 and also shows expression of the system.
-We can see that we have two bands on the gel, one is approximately 30 kDa which is the size of the fusion protein Aga2-CUP1-GGGGSEAAAKGGGGS-CUP1-V5 and the other is slightly smaller. The smaller band could be a truncated version of the protein since we identified a second in-frame start codon in the DNA sequence. Unfortunately the truncated version seems to be the most expressed one, corresponding to the signal intensity.
-The presence of our CUP1 dimer in our yeast transformants is thus shown.
-'''Immunostaining'''
-[[File:BBa_K4035007-immuno_image_1.jpg|400px|thumb|right|'''Figure 2a''' : Immunostaining of the yeast transformed with the pCTcon2-CUP1-GGGGSEAAAKGGGGS-CUP1-V5 plasmid]]
-To show that the fusion protein is expressed at the membrane of the cell we performed an Immunostaining. The cells are incubated with a primary mouse anti-V5 antibody as well as with a secondary goat anti-mouse couple with Alexa Fluor Plus, a green fluorophore. The same strains for control have been used namely, plasmid backbone induced ('''Figure 2c''') and wild type yeast ('''Figure 2d''').
-The nuclei have been stainined with DAPI and are depicted in blue on the figures. The green disks are representing the
-the recombinant yeast cells expressing the CUP1 dimer at their surface ('''Figure 2a''').
-Due to the more intense circle we can clearly see that our system is expressed on the membrane of the protein (this is better seen on '''Figure 2b''' which the higher magnification picture of yeast transformed with a single copy of CUP1, part [https://parts.igem.org/Part:BBa_K4035001 BBa_K4035001]). As these are non permeabilized cells, the antibodies bind only the extracellular proteins.
-We can also remark that not all the cells are expressing the system. This is because the expression is not 100% efficient.
-On the negative control, the little green signal we see is background noise or unspecific antibody binding.
-[[File:BBa_K4035001-immuno_image_2bis.jpg|400px|thumb|left|'''Figure 2b''' : Immunostaining of the yeast transformed with the pCTcon2-CUP1-V5 plasmid ([https://parts.igem.org/Part:BBa_K4035001 BBa_K4035001]), green channel, 40x magnification]]
-[[File:BBa_K4035001-immuno_image_3bis.jpg|400px|thumb|right|'''Figure 2c''' : Immunostaining of the the wild type EBY100 yeast]]
-[[File:BBa_K4035001-immuno_image_4.jpg|400px|thumb|left|'''Figure 2d''' : Immunostaining of the yeast transformed with backbone plasmid pCTcon2V5]]
+==Characterization==
+===Expression of the protein in S.cerevisiae===
+'''Western Blot Analysis'''
+[[File:BBa_K4035007_WEB_image_1.jpg|400px|thumb|right|'''Figure 1''' : V5 tagged CUP1 dimer expression in the yeast S.cerevisiae]]
+In order to characterize the protein expression, two experiments were performed, the first being a Western Blot analysis. After having transformed the EBY100 yeast with our newly formed plasmid pCTcon2-dimer-V5, we analyzed its protein expression. For control we also tested the wild type yeast (untransformed) as well as a transformed yeast with the plasmid backbone (without insert) in SGCAA, a medium containing galactose allowing for protein expression through the activation of the Gal1 promoter. As the plasmid contains a Gal1 promoter, the system can only be expressed in the presence of galactose.
+'''Figure 1''' : The first lane (E2) is the yeast transformed with our plasmid containing the CUP1 dimer and the second and third lanes are, respectively, plasmid backbone and wild type yeast. EBY100 is the wild type yeast and serves as a negative control whereas pCTcon2-V5 is the transformed yeast with only the plasmid backbone and serves as a positive control.
+Wild type yeast shows no presence of the V5 tag, as expected, while plasmid backbone has signal which proves that our system is expressed in the transformed yeast when induced with galactose. Our transformed yeast with the Aga2-CUP1-linker-CUP1-V5 protein also shows expression of the system.
+We can see that we have two bands on the gel, one is approximately 30 kDa which is the size of the fusion protein Aga2-CUP1-linker-CUP1-V5 and the other is slightly smaller. The smaller band could be a truncated version of the protein since we identified a second in-frame start codon in the DNA sequence.
+The presence of our CUP1 dimer in our yeast transformants is thus shown.
+'''Immunocytochemistry Assay'''
+[[File:BBa_K4035007-immuno_image_1.jpg|400px|thumb|right|'''Figure 2a''' : V5 tagged CUP1 dimer membrane expression in the yeast S.cerevisiae]]
+To show that the fusion protein is expressed at the membrane of the cell we performed an Immunocytochemistry assay. The cells were incubated with a primary mouse anti-V5 antibody as well as with a secondary goat anti-mouse couple with Alexa Fluor 488. The same strains for control have been used namely, plasmid backbone induced ('''Figure 2c''') and wild type yeast ('''Figure 2d''').
-===Growth and Survival Characterization===
+The nuclei have been stained with DAPI and are depicted in blue on the figures. The green disks are representing
-'''Growth curves of the different yeast strains'''
+the transformed yeast cells expressing the CUP1 dimer at their surface ('''Figure 2a''').
-In order to check if our expression system would affect the growth of our micro-organism, we performed multiple growth curves with different parameters.
+Due to the more intense circle we can clearly see that our system is expressed on the membrane of the protein (better seen on '''Figure 2b''' which is a higher magnification picture of yeast transformed with a single copy of CUP1, part [https://parts.igem.org/Part:BBa_K4035001 BBa_K4035001]).
-'''Colony forming assays of the different yeast strains'''
+We can also remark that not all the cells are expressing the system. This is because the expression is not 100% efficient, concordant to the published expression system (1).
-A second experiment was done to check if the expression system would affect the growth of the yeast cells, a colony forming assay. That experiment consisted of counting the colonies formed by the different yeast strains, respectively wild type, backbone uninduced, backbone induced and transformant, on agar plates.
+On the negative control, the little green signal we see is background noise or nonspecific antibody binding.
-'''Copper absorption assays'''
+[[File:BBa_K4035001-immuno_image_2bis.jpg|400px|thumb|left|'''Figure 2b''' : V5 tagged CUP1 membrane expression in the yeast S.cerevisiae ([https://parts.igem.org/Part:BBa_K4035001 BBa_K4035001]), 488 nm excitation channel, 40x magnification]]
+[[File:BBa_K4035001-immuno_image_3bis.jpg|400px|thumb|right|'''Figure 2c''' : EBY100, negative control]]
+[[File:BBa_K4035001-immuno_image_4.jpg|400px|thumb|left|'''Figure 2d''' : V5 tag membrane expression in the yeast S.cerevisiae]]
-To finally test our system we imagined an experiment to measure how muchcopper our transformed yeast could absorb.
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