Difference between revisions of "Part:BBa K3190103"

Revision as of 11:58, 20 October 2019

G protein-coupled estrogen receptor (GPER) CDS with Linker-superfolder GFP

G protein-coupled estrogen receptor (GPR30, also referred to as GPER), an intracellular transmembrane estrogen receptor, was identified in 2005 (Revankar, 2005). It is found to localise to the endoplasmic reticulum and specifically binds to estrogen and its derivatives. The interaction between estradiol and the membrane-associated receptor triggers non-genomic signalling; intracellular calcium mobilization and synthesis of phosphatidylinositol 3,4,5-trisphosphate in the nucleus. For this biobrick, C-terminal end of GPER (BBa K3190101) was fused with superfolder GFP (BBa_K3190205) using a linker (BBa_K3190206).

Usage and Biology

In our studies, GPER-Li-sfGFP was used to examine expression and localization of GPER (BBa_K3190101) in S. cerevisiae.

Chromosomal integration

For our studies, GPER-Li-sfGFP was integrated into the yeast chromosome, and correct insertion was verified using colony PCR.

Figure 2: Colony PCR of yeast transformed with GPER-Li-sfGFP | Specific yeast genotyping primers were used for the PCR reaction. PCR products were separated by electropheresis on 1% agarose gel. The sizes of the molecular weight standards are shown on the left. Lanes 1-8 correspond to individual colonies. Expected band sizes are of 1000 bp, indicating successful chromosomal integration. Band sizes of 1500 bp indicate unsuccesful chromosomal integration.

Expression of G protein-coupled estrogen receptor

The expression of the GPER-li-sfGFP was confirmed by performing western blot, using anti GFP antibody. The results are depicted below:

Figure 3: Western blot of insoluble vs soluble cellular protein | Western blot was carried out using anti-GFP antibodies. Yeast expressing empty vectors was taken as negative control. Yeast expressing GFP was taken as positive control. All blue prestained protein standards was the ladder used for comparison.

The positive and negative control have worked as expected. GFP was so strongly expressed in the positive control cells that is was even seen in the insoluble fraction. Vice versa, GPER-sfGFP was predominant in the insoluble fraction, which we expected since it is a membrane protein. A small band can however also be seen in the soluble fraction, indicating that the protein is very abundant in the respective cells.

Microscopy

To determine the expression of GFP and intracellular localization of the receptor, confocal microscopy was performed with yeast expressing GPER-Li-sfGFP and yeast expressing empty vectors (negative control).

Figure 4: Confocal microscopy of transformed yeast cells. A and B depict bright field vs fluorescence filter showing yeast expressing empty vector backbones. C and D depict bright field vs fluorescence filter showing yeast expressing GPER-sfGFP.

Yeast strain containing empty vectors was visible on the bright field (A) but not on fluorescence filter (B) as expected as there is no sfGFP. Whereas, yeast strain containing sfGFP was visible on both bright field (C) and fluorescence filter (D) due to the expression of sfGFP, which confirms the expression of GPER as GFP is tagged to the C-terminal of the receptor. From (D) it also looks like GPER-sfGFP might have been expressed in the endoplasmic reticulum (ER).

Sequence and Features