"

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-	==Data Page==	+	==Experiment Results / Discussion ==
-	===BBa_K1202100 – Nanofactory Binding Zone (C215)===	+	===-The Experiments about EpCAM – Anti EpCAM Binding===
-	This is the primary section of NanoFactory design. This part is one of the active domains of anti-EpCAM (Epithelial Cell Adhesion Molecule) antibody. We use this part in our NanoFactory system as a binding zone to EpCAM antigen. We added additional histidine tag for purification purposes. Also we added a linker sequence; thus, we want to prevent misfolding in our proteins.	+	First of all, we wanted to test if our bacteria were able to produce C215 (Anti-EpCAM). To determine this, we performed Immunofluorescence experiments by placing OmpA (a signal peptide which sends the proteins into the membrane) signal peptide and his-tag before the C215 protein sequence in one of our parts. We then accomplished immunofluorescence colouring and were able to see red circles around our bacteria. ''Including his-tag in the sequence was to our bacteria.'' During the experiments we used anti-his-tag which was situated after the colouring substance in the sequence. This allowed us to comprehend if our bacteria were able to produce C215; in which case they were.
-	===BBa_K1202101 – Nanofactory Enzyme Zone (LuxS-Pfs)===	+
-	Second section of NanoFactory consists of an enzyme complex which is responsible for the transformation reaction of S-adenosyl homocysteine (SAH) into autoinducer-2 (AI-2) quorum sensing unit. We planned to use this part as an attractor for bacteria after cancer cells are detected and stabilized by NanoFactory Binding Zone (BBa_K1202100).	+	Our second set of immunofluorescence experiments was to confirm the binding of EpCAM to C215. The first set of experiments had proved that our bacteria were successfuly producing C215, however we were unable to comprehend if C215 was able to bind to EpCAM or not. Therefore we carried out another experiment, where purified C215 was presented to cancer cells in well-plates. Our expectations were fulfilled and we were able to see red coloured cancer cells and blue nucleus'.
-	===BBa_K1202102 – Nanofactory Connecting Domain (Protein G)===	+
-	Protein G is used as a protein linker domain and antibody Fc section binding tag in literature. In our design, NanoFactory consists of two main sections: Binding and enzyme zones. By linking these two sections with Protein G, we hope to conduct excellent protein folding and less complication in our experiments. Additionally, we want to use the Fc binding ability of Protein G for the alternative NanoFactory binding zone construction technique.	+
-	===BBa_K1202103 – TAT-Apoptin with HlyA Signal Peptide===	+	-------------------------------------------------------------------------
-	Our cancer killing system, TAT-Apoptin, must be secreted from our bacteria. For this purpose, we decided to add HlyA signal peptide in the downstream region of our part. HlyA works only if it is placed in the N-terminus of protein. With this design, our TAT-Apoptin system can go out from bacteria.	+
-	===BBa_K1202104 – TorA-GFP===	+
-	This construct is designed to test our TorA signal peptide function. In our plan, produced green fluorescent protein (GFP) must diffuse into the media via this signal peptide. Thus, this should allow us to measure it with excitation and emission assay.	+	[[File:Oncoli-exp1-i1.jpg|800px]]
-	===BBa_K1202105 – TAT-Apoptin: Cancer killing peptide===	+
-	TAT-Apoptin was designed to induce programmed cell death (apoptosis) in cancer cells, selectively.  TAT signal peptide added to direct apoptin into cancer cells.	+
-	===BBa_K1202106 – TAT-HA2-Apoptin: Cancer killing peptide===	+	---
-	HA2 peptide sequence is demonstrated that, with the combination of TAT, the cell penetrating activity increases considerably. We added HA2 in our TAT-Apoptin system to empower the yield of cancer killing mechanism.	+
-	===BBa_K1202107 – TAT-E4-orf4: Cancer killing peptide===	+	[[File:Oncoli-exp1-i2.jpg|800px]]
-	The general attitude to our parts is to designate alternative parts. For cancer killing mechanism, we searched through literature and found E4orf4 peptide. This derivative prospective cancer drug, like apoptin, induces apoptosis in cancer cells, selectively. Moreover, in literature and, of course iGEM, TAT-E4orf4 combination is completely novel.	+
-	===BBa_K1202108 – pLsr promoter and LsrR Generator===	+
-	Lsr operon is one of the existing operons in E.coli for selective production of designated proteins in different conditions. This production chain is regulated strictly by using repressors and activators. In Lsr system, LsrR is the main repressor of the promoter and can only be inhibited by the presence of phosphorylated autoinducer-2 (AI-2) quorum sensing unit. (see diagram) We want to use this part to conduct cancer detecting mechanism in bacteria.	+	[[File:Oncoli-exp1-i3.jpg|800px]]
-	===BBa_K1202109 – LsrK Generator===	+
-	Lsr system consists of three components, mainly. Lsr promoter, LsrR repressor and LsrK enzyme. This enzyme works as phosphorylase that catalyzes AI-2 phosphorylation reactions. AI-2-phosphorus complex allows the inhibition of repression effect of LsrR on Lsr promoter and provides the production of desired protein. Via this system, we want to regulate the production of our cancer killing peptides.	+	[[File:Oncoli-exp1-i4.jpg|800px]]
-	===BBa_K1202110 – AI-2 Generator (LuxS-Pfs)===	+
-	Alternative to our NanoFactory design, we plan to use our E.coli as a nano scale cancer searching device by presenting NanoFactory Binding Zone on the outer membrane and, in the case of detection, signal transmitter by producing AI-2 into the media. This part works as NanoFactory Enzyme Zone in bacteria by transforming intracellular SAH into AI-2.	+	[[File:Oncoli-exp1-i5.jpg|800px]]
-	===BBa_K1202111 – MPG-Apoptin: Cancer killing peptide===	+
-	We decided to use an alternative cell penetrating peptide instead of TAT. Likewise, MPG directs the attached protein into the eukaryotic cell cytoplasm. We want to use this activity to conduct our apoptosis inducing effect of our cancer killing proteins.	+
-	===BBa_K1202112 – GFP-HlyA===	+
-	This construct is designed to test our HlyA signal peptide function. In our plan, produced green fluorescent protein (GFP) must diffuse into the media via this signal peptide. Thus, this should allow us to measure it with excitation and emission assay.	+
-	===BBa_K1202113 – TAT-RFP===	+	====Immunofluorescence c215====
-	This part is designed to measure the cell penetrating effect of TAT peptide. In our plan, in the case of good penetration, we could emit red fluorescent in cancer cell cytoplasm. This would allow us to say that our TAT directs the desired proteins into the cells efficiently.	+	For our project to work, the active domain of anti EpCAM was required to bind to the membranes of cancer cells. Pic. 1 show vague red shining cells which prove that our C215 is working. With these results we were able to say that our nanofactories would be able to bind to our cancer cells successfully.
-	===BBa_K1202114 – C215 Presenting Dock (With OmpA)===	+
-	OmpA is widely used transmembrane, antigen presenting protein in literature and iGEM, and also, is used as a signal peptide. We want to use as an advantage and use it in our alternative NanoFactory design which proposes to use our E.coli as NanoFactory. OmpA will allow us to present NanoFActory Binding Domain on outside of bacteria cell wall. This would ends with the efficient binding of bacteria on cancer cells.	+	====Immunofluorescence OmpA====
-	===BBa_K1202115 – TorA-TAT-Apoptin===	+	Before beginning with experiments we decided to use an alternative method to detect the cancer cells. We decided to use our bacteria as nanofactory itself (quorum sensing). Therefore OmpA was placed before C215 to determine so that our bacteria would bind to the cancer cells. We tested the production of OmpA by our bacteria with immunofluorescence experiments and were able to see shinning red lights in the Pic 2 which proved that our OmpA was presented by our cell’s outer membrane successfully; meaning that our bacteria could be used as a nanofactory.
-	This part is designed to measure the secretion potency of our signal peptide, TorA, for our cancer killing peptides. To provide this, we plan to perform SDS-PAGE and Western blotting assays in supernatant samples by adding histidine tags to our peptides.	+	=Ellmans Assay=
-	===BBa_K1202116 – pLsr Complete System (Receiver)===	+	Ellman’s assay is a test which enables us to measure the concentration of AI-2. In order to perform Ellman’s assay liquid culture of bacteria which produce the enzymes Luxs-Pfs were required. The liquid cultures resistant to CHL were incubated for 16 hours which then followed on by adding 0,1 mM substrate (SAH in 10X PBS containing %1 BSA) and SAH containing liquid cultures were continued to be incubated but this time at room temprature for a period of two hours. During the incubations, our enzymes were producing autoinducer 2. To determine the quantity of autoinducer-2 produced, we centrifuged and measured light density of our supernatants with the light spectrophotometer. Our negative control  were transformed bacteria. The results of the Ellman’s assay our below:
-	This is the combination of the parts “pLsr promoter and LsrR Generator” and “LsrK Generator”. This is the final design for Lsr system and allows us to measure the quorum sensing potency of autoinducer-2 (AI-2) stimulation and Lsr promoter production ability.	+
		+	This results show that enzymes are expressed by e.coli are succesfully producing autoinducer2.
		+	===Lsrk/ Lslr Inducible promoter experiment===
		+	To observe inducible promoters response, we co incubated two different bacteria. The first bacteria culture was expressing the enzyme system luxs-pfs and the second culture included our inducible promoter which produce RFP in the presence of AI-2. During the experiment, we incubated them seperately for 16 hours then mixed them into one flask and waited for 4 hours, we then add 0,1 mM SAH (with 10x PBS containing %1 BSA). After incubating them with SAH for one day, we took 2 ml of liquid culture into centrifuge tubes for centrifugation. Below is a photo which shows the resulting red pellet of our experiment meaning that our inducible promoter was succesfully working to produce AI-2.
		+
		+
		+	[[File:Oncoli-exp1-i7.jpg|800px]]
		+
		+	===Discussion of ellman’s assay===
		+	Our results proved that our system was working as expected and the challenges were overcome. According to our Ellman’s assay experience, our enzyme system is succesfully producing auto inducer 2. As described in the ‘design’ section, AI-2 will induce bacteria to move towards the cancer cells.
		+	We searched for an inducible system which would become activated at the presence of antigen on bacteria. As an activating molecule, autoinducer2 activates LsrR-LsrK promoter system for express the killer protein by bacteria.
		+	The centrifuged tubes of liquid cultures were addedwith an inducible promoter containing the RFP gene which would be a marker of its activation. Therefore the results of co-incubation significantly show us that the promoter system is activated in the presence of autoinducer-2.
		+
		+	==Protein G binding experiment==
		+	Our nanofactory is formed with an antibody, Protein G and an enzyme complex. A connection between the enzyme system and antibody was required, therefore we used a linker. We used a molecule called protein G which was derived from group C and G Streptococcus strains that binds to the Fc region of numerous immunogloblulins. Protein G facilitates binding of enzyme construct to the Fc region of the targeting antibody. We also cloned the nanofactories into pSB1C3 and we expressed this protein in the BL21 strain of E. coli. Futhermore we tagged his6x at N terminus of protein G for purification.
		+
		+	The aim of protein G and Ig G binding experiment was to construct a nanofactory complex composed of two parts that is the antibody and enzyme system.
		+	Protein G has a natural affinity  to bind to the antibody in phosphate buffer. Therefore we incubated protein G with the antibodies in 10mM phosphate buffer for 2,5 hours and measured the quantity of fused proteins via Western Blotting experiment.
		+	Result;
		+
		+
		+	[[File:Oncoli-exp1-i8.jpg|800px]]
		+
		+
		+	Our protein G weight was 25 kDas and our combined Protein G + antibody protein’s weight was about 50 kDas.  In our view, the experimental results were acceptable as the weight of protein G is known to be approximately 25 kDas line as well as the complex being close 50 kDas.
		+
		+	==DISCUSSION==
		+	First of all, liquid culture was prepared for our TorA-GFP and GFP-HlyA experiments. We added TritonX into half of our TorA-GFP samples and didn’t add any chemicals into the other half of TorA-GFP samples . After the Overnight process of incubation we centrifuged to receive our supernatants from our samples because our aim was to extract the proteins.
		+	The results of the TorA-GFP supernatant samples showed that the samples with TritonX & Glycine had no GFP. We assumed this was due to the cellular necroses due to TritonX & glycine being high in concentration  caused secretion of low amount of GFP. Because of the secretion of the GFP in periplasmic gap we used %2 TritonX*+%1 Glycine*  that wrote in article and we destroy outer memrane. We got this concentration from article.
		+	Our TorA-GFP experiment results show that the samples with only TritonX added contains more GFP than the Negative(-) Control. The results show us that our signal peptides worked properly and our chemicals TritonX and Glycine showed the right effects of our desires.
		+	GFP-HlyA also resulted in the production of high amount of GFP in our Negative(-) Controls.
		+	Another set of results showed that liquid culture of only LB produced maximum amount of GFP.
		+
		+	*Tang et al 2008 ., Jin-bao Tanga, Hong-ming Yanga, Shu-liang Songb, Peng Zhub, Ai-guo Jib
		+	(Effect of Glycine and Triton X-100 on secretion and expression of ZZ–EGFP fusion protein)
		+	1)Blobel G, Dobberstein B. (Dec. 1975). "Transfer of proteins across membranes. I. Presence of proteolytically processed and unprocessed nascent immunoglobulin light chains on membrane-bound ribosomes of murine myeloma."
		+
		+
		+	===Optimization of constitutive promoter for protein over expression===
		+	The over expression experiments aim was to increase the synthesis of our protein in a new medium we prepared. We predicted that the over expression of our desired protein by our bacteria would be a good idea to observe the net results. So we decided to prepare the “best medium” for the bacteria. Then we generated different media combinations. We generated the combinations by altering conditions of bacteria, liquid culture incubation time, bacteria strain and temperature of incubator. So at the end of the experiment there were 60 different conditions and media we designed.
		+	Different media and conditions in our experiment:
		+
		+
		+	[[File:Oncoli-exp1-i10.jpg|800px]]
		+
		+	After preparing the media we started the experiment stage. Our experiment includes protein isolation and SDS page parts.  We got the total amount of protein of the bacteria after the protein isolation by using sonicator. Then we measure the band of our proteins in the SDS Page experiment. Finally we chose the winner a medium called TNY, BL21, 24H, 37C
		+	SDS Page results;
		+
		+
		+	[[File:Oncoli-exp1-i11.png|800px]]
		+	TNY, BL21, 37C, 24Hr                        TNY, NEB10, 37C, 24Hr
		+
		+
		+	We were excepting LB as the expression maximizer but the results were surpising as the TNY medium resulted in high level of protein. İngredients of LB and TNY were the same. The only difference was the concentration of each component. Interestingly, the medium with low density was better than our routine medium, LB. There was small percentage dissimilarity between the medias like 7/200 and 4/200. Our TNY was prepared by diluting 4gr TNY extract with distilled water.
		+	To conclude, protein expression level of TNY is 10  times higher than LB(see above).
		+
		+	==Signal Peptide ==
		+	A signal peptide (sometimes referred to as signal sequence, leader sequence or leader peptide) is a short (5-30 amino acids long) peptidepresent at the N-terminus of the majority of newly synthesized proteins that are destined towards the secretory pathway.[1]
		+	In prokaryotes, signal peptides direct the newly synthesized protein to the SecYEG protein-conducting channel, which is present in the plasma membrane.
		+	In this part of our project we tested are our signal peptides is working or not
		+	To secrete GFP protein via signal peptide to extracellular membrane.
		+	In overall project, our aim related with signal peptide is to secrete apoptotic proteins outer membrane. If this construct secrete GFP successfully, that means signal peptide works and TorA can be used in Apoptin or E4orf4 export.
		+	And also we use constitutive promoter in our designs because we need high amount of protein and we want to our bacteria always produce our proteins.
		+	We made santrifuge our signal peptides’ (TorA-GFP ve GFP-HlyA) liquid culture falcons and then get supernatant from falcons. Then we measured values of absorption of GFP in our supernatant in suitable wavelength. Results show that we found high amount of GFP in our supernatants.
		+	Result;
		+
		+
		+	[[File:Oncoli-exp1-i9.jpg|800px]]
		+
		+	Column scale(y) shows us quantity amount of GFP in the solution.
		+
		+
		+	==DISCUSSION==
		+	Firstly we made liquid culture in our TorA-GFP and GFP-HlyA experiments. We added TritonX half of our TorA-GFP samples and didn’t add any chemicals our other TorA-GFP samples . After the Overnight process we made santrifuge and we get supernatants from our samples because we wait our proteins in supernatant.
		+	The results of the supernatant of the TorA-GFP samples that we didn’t add TritonX & Glycine were over 0. So we thought that we got this results becuse of the cellular necroses that caused secretion of low amount of GFP. Because of the secretion of the GFP in periplasmic gap we used %2 TritonX*+%1 Glycine*  that wrote in article and we destroy outer memrane. We got this concentration from article.
		+	Our results in our TorA-GFP experiments that our samples that added TritonX contains more GFP amount than Negative(-) Control. So this results showed us that our signal peptides worked properly and our chemicals TritonX and Glycine showed their effects.
		+	Also we get another fine results from our GFP-HlyA that we found high amount of GFP in our samples more than our Negative(-) Control.
		+	Another good results that our Positive Control which is GFP that added in LB showed maximum amount of GFP in graphics. So we can said that our controls were working too.
		+	*Tang et al 2008 ., Jin-bao Tanga, Hong-ming Yanga, Shu-liang Songb, Peng Zhub, Ai-guo Jib
		+	(Effect of Glycine and Triton X-100 on secretion and expression of ZZ–EGFP fusion protein)
		+	1)Blobel G, Dobberstein B. (Dec. 1975). "Transfer of proteins across membranes. I. Presence of proteolytically processed and unprocessed nascent immunoglobulin light chains on membrane-bound ribosomes of murine myeloma."
		+
		+
		+
		+	We were excepting the LB for the winner of the experiment but we surprised by seeing the result.  Because the medium that prepared by us and called TNY was the best. The content of TNY and LB is the similar but the component percentage of media is different. It is very interesting that low rated medium is better than the LB. There is small percentage dissimilarity between the media like 7/200 and 4/200. Our TNY is preparing by diluting 4 gr TNY extract with distilled water.
		+	We observed the protein expression level of TNY 10 times more than LB as you see above.

---

Latest revision as of 15:08, 19 May 2014

Contents 1 Experiment Results / Discussion 1.1 -The Experiments about EpCAM – Anti EpCAM Binding 1.1.1 Immunofluorescence c215 1.1.2 Immunofluorescence OmpA 2 Ellmans Assay 2.1 Lsrk/ Lslr Inducible promoter experiment 2.2 Discussion of ellman’s assay 2.3 Protein G binding experiment 2.4 DISCUSSION 2.4.1 Optimization of constitutive promoter for protein over expression 2.5 Signal Peptide 2.6 DISCUSSION

Experiment Results / Discussion

-The Experiments about EpCAM – Anti EpCAM Binding

First of all, we wanted to test if our bacteria were able to produce C215 (Anti-EpCAM). To determine this, we performed Immunofluorescence experiments by placing OmpA (a signal peptide which sends the proteins into the membrane) signal peptide and his-tag before the C215 protein sequence in one of our parts. We then accomplished immunofluorescence colouring and were able to see red circles around our bacteria. Including his-tag in the sequence was to our bacteria. During the experiments we used anti-his-tag which was situated after the colouring substance in the sequence. This allowed us to comprehend if our bacteria were able to produce C215; in which case they were.

Our second set of immunofluorescence experiments was to confirm the binding of EpCAM to C215. The first set of experiments had proved that our bacteria were successfuly producing C215, however we were unable to comprehend if C215 was able to bind to EpCAM or not. Therefore we carried out another experiment, where purified C215 was presented to cancer cells in well-plates. Our expectations were fulfilled and we were able to see red coloured cancer cells and blue nucleus'.

---

---

Immunofluorescence c215

For our project to work, the active domain of anti EpCAM was required to bind to the membranes of cancer cells. Pic. 1 show vague red shining cells which prove that our C215 is working. With these results we were able to say that our nanofactories would be able to bind to our cancer cells successfully.

Immunofluorescence OmpA

Before beginning with experiments we decided to use an alternative method to detect the cancer cells. We decided to use our bacteria as nanofactory itself (quorum sensing). Therefore OmpA was placed before C215 to determine so that our bacteria would bind to the cancer cells. We tested the production of OmpA by our bacteria with immunofluorescence experiments and were able to see shinning red lights in the Pic 2 which proved that our OmpA was presented by our cell’s outer membrane successfully; meaning that our bacteria could be used as a nanofactory.

Ellmans Assay

Ellman’s assay is a test which enables us to measure the concentration of AI-2. In order to perform Ellman’s assay liquid culture of bacteria which produce the enzymes Luxs-Pfs were required. The liquid cultures resistant to CHL were incubated for 16 hours which then followed on by adding 0,1 mM substrate (SAH in 10X PBS containing %1 BSA) and SAH containing liquid cultures were continued to be incubated but this time at room temprature for a period of two hours. During the incubations, our enzymes were producing autoinducer 2. To determine the quantity of autoinducer-2 produced, we centrifuged and measured light density of our supernatants with the light spectrophotometer. Our negative control were transformed bacteria. The results of the Ellman’s assay our below:

This results show that enzymes are expressed by e.coli are succesfully producing autoinducer2.

Lsrk/ Lslr Inducible promoter experiment

To observe inducible promoters response, we co incubated two different bacteria. The first bacteria culture was expressing the enzyme system luxs-pfs and the second culture included our inducible promoter which produce RFP in the presence of AI-2. During the experiment, we incubated them seperately for 16 hours then mixed them into one flask and waited for 4 hours, we then add 0,1 mM SAH (with 10x PBS containing %1 BSA). After incubating them with SAH for one day, we took 2 ml of liquid culture into centrifuge tubes for centrifugation. Below is a photo which shows the resulting red pellet of our experiment meaning that our inducible promoter was succesfully working to produce AI-2.

Discussion of ellman’s assay

Our results proved that our system was working as expected and the challenges were overcome. According to our Ellman’s assay experience, our enzyme system is succesfully producing auto inducer 2. As described in the ‘design’ section, AI-2 will induce bacteria to move towards the cancer cells. We searched for an inducible system which would become activated at the presence of antigen on bacteria. As an activating molecule, autoinducer2 activates LsrR-LsrK promoter system for express the killer protein by bacteria. The centrifuged tubes of liquid cultures were addedwith an inducible promoter containing the RFP gene which would be a marker of its activation. Therefore the results of co-incubation significantly show us that the promoter system is activated in the presence of autoinducer-2.

Protein G binding experiment

Our nanofactory is formed with an antibody, Protein G and an enzyme complex. A connection between the enzyme system and antibody was required, therefore we used a linker. We used a molecule called protein G which was derived from group C and G Streptococcus strains that binds to the Fc region of numerous immunogloblulins. Protein G facilitates binding of enzyme construct to the Fc region of the targeting antibody. We also cloned the nanofactories into pSB1C3 and we expressed this protein in the BL21 strain of E. coli. Futhermore we tagged his6x at N terminus of protein G for purification.

The aim of protein G and Ig G binding experiment was to construct a nanofactory complex composed of two parts that is the antibody and enzyme system. Protein G has a natural affinity to bind to the antibody in phosphate buffer. Therefore we incubated protein G with the antibodies in 10mM phosphate buffer for 2,5 hours and measured the quantity of fused proteins via Western Blotting experiment. Result;

Our protein G weight was 25 kDas and our combined Protein G + antibody protein’s weight was about 50 kDas. In our view, the experimental results were acceptable as the weight of protein G is known to be approximately 25 kDas line as well as the complex being close 50 kDas.

DISCUSSION

First of all, liquid culture was prepared for our TorA-GFP and GFP-HlyA experiments. We added TritonX into half of our TorA-GFP samples and didn’t add any chemicals into the other half of TorA-GFP samples . After the Overnight process of incubation we centrifuged to receive our supernatants from our samples because our aim was to extract the proteins. The results of the TorA-GFP supernatant samples showed that the samples with TritonX & Glycine had no GFP. We assumed this was due to the cellular necroses due to TritonX & glycine being high in concentration caused secretion of low amount of GFP. Because of the secretion of the GFP in periplasmic gap we used %2 TritonX*+%1 Glycine* that wrote in article and we destroy outer memrane. We got this concentration from article. Our TorA-GFP experiment results show that the samples with only TritonX added contains more GFP than the Negative(-) Control. The results show us that our signal peptides worked properly and our chemicals TritonX and Glycine showed the right effects of our desires. GFP-HlyA also resulted in the production of high amount of GFP in our Negative(-) Controls. Another set of results showed that liquid culture of only LB produced maximum amount of GFP.

• Tang et al 2008 ., Jin-bao Tanga, Hong-ming Yanga, Shu-liang Songb, Peng Zhub, Ai-guo Jib

(Effect of Glycine and Triton X-100 on secretion and expression of ZZ–EGFP fusion protein) 1)Blobel G, Dobberstein B. (Dec. 1975). "Transfer of proteins across membranes. I. Presence of proteolytically processed and unprocessed nascent immunoglobulin light chains on membrane-bound ribosomes of murine myeloma."

Optimization of constitutive promoter for protein over expression

The over expression experiments aim was to increase the synthesis of our protein in a new medium we prepared. We predicted that the over expression of our desired protein by our bacteria would be a good idea to observe the net results. So we decided to prepare the “best medium” for the bacteria. Then we generated different media combinations. We generated the combinations by altering conditions of bacteria, liquid culture incubation time, bacteria strain and temperature of incubator. So at the end of the experiment there were 60 different conditions and media we designed. Different media and conditions in our experiment:

After preparing the media we started the experiment stage. Our experiment includes protein isolation and SDS page parts. We got the total amount of protein of the bacteria after the protein isolation by using sonicator. Then we measure the band of our proteins in the SDS Page experiment. Finally we chose the winner a medium called TNY, BL21, 24H, 37C SDS Page results;

           TNY, BL21, 37C, 24Hr                        TNY, NEB10, 37C, 24Hr

We were excepting LB as the expression maximizer but the results were surpising as the TNY medium resulted in high level of protein. İngredients of LB and TNY were the same. The only difference was the concentration of each component. Interestingly, the medium with low density was better than our routine medium, LB. There was small percentage dissimilarity between the medias like 7/200 and 4/200. Our TNY was prepared by diluting 4gr TNY extract with distilled water. To conclude, protein expression level of TNY is 10 times higher than LB(see above).

Signal Peptide

A signal peptide (sometimes referred to as signal sequence, leader sequence or leader peptide) is a short (5-30 amino acids long) peptidepresent at the N-terminus of the majority of newly synthesized proteins that are destined towards the secretory pathway.[1] In prokaryotes, signal peptides direct the newly synthesized protein to the SecYEG protein-conducting channel, which is present in the plasma membrane. In this part of our project we tested are our signal peptides is working or not To secrete GFP protein via signal peptide to extracellular membrane. In overall project, our aim related with signal peptide is to secrete apoptotic proteins outer membrane. If this construct secrete GFP successfully, that means signal peptide works and TorA can be used in Apoptin or E4orf4 export. And also we use constitutive promoter in our designs because we need high amount of protein and we want to our bacteria always produce our proteins. We made santrifuge our signal peptides’ (TorA-GFP ve GFP-HlyA) liquid culture falcons and then get supernatant from falcons. Then we measured values of absorption of GFP in our supernatant in suitable wavelength. Results show that we found high amount of GFP in our supernatants. Result;

Column scale(y) shows us quantity amount of GFP in the solution.

DISCUSSION

Firstly we made liquid culture in our TorA-GFP and GFP-HlyA experiments. We added TritonX half of our TorA-GFP samples and didn’t add any chemicals our other TorA-GFP samples . After the Overnight process we made santrifuge and we get supernatants from our samples because we wait our proteins in supernatant. The results of the supernatant of the TorA-GFP samples that we didn’t add TritonX & Glycine were over 0. So we thought that we got this results becuse of the cellular necroses that caused secretion of low amount of GFP. Because of the secretion of the GFP in periplasmic gap we used %2 TritonX*+%1 Glycine* that wrote in article and we destroy outer memrane. We got this concentration from article. Our results in our TorA-GFP experiments that our samples that added TritonX contains more GFP amount than Negative(-) Control. So this results showed us that our signal peptides worked properly and our chemicals TritonX and Glycine showed their effects. Also we get another fine results from our GFP-HlyA that we found high amount of GFP in our samples more than our Negative(-) Control. Another good results that our Positive Control which is GFP that added in LB showed maximum amount of GFP in graphics. So we can said that our controls were working too.

• Tang et al 2008 ., Jin-bao Tanga, Hong-ming Yanga, Shu-liang Songb, Peng Zhub, Ai-guo Jib

(Effect of Glycine and Triton X-100 on secretion and expression of ZZ–EGFP fusion protein) 1)Blobel G, Dobberstein B. (Dec. 1975). "Transfer of proteins across membranes. I. Presence of proteolytically processed and unprocessed nascent immunoglobulin light chains on membrane-bound ribosomes of murine myeloma."

We were excepting the LB for the winner of the experiment but we surprised by seeing the result. Because the medium that prepared by us and called TNY was the best. The content of TNY and LB is the similar but the component percentage of media is different. It is very interesting that low rated medium is better than the LB. There is small percentage dissimilarity between the media like 7/200 and 4/200. Our TNY is preparing by diluting 4 gr TNY extract with distilled water. We observed the protein expression level of TNY 10 times more than LB as you see above.