Hay fever curE2013.igem.org/files/presentation/KAIT_Japan.pdf · We produce IL12 with this...
Transcript of Hay fever curE2013.igem.org/files/presentation/KAIT_Japan.pdf · We produce IL12 with this...
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Hay fever curE.coli
KAIT-JAPAN
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Background
Take a medicine (anti-allergic drug and antihistamine drug)
Hay fever measures…
But … There is a difference in the case of an individual drug of hay fever, some people side effects such as thirst and sleepiness may appear.
In JAPAN
One of six person are developed
hay fever.
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What is Hay fever?
Invasion
Human
Pollen
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Lymphocyte Pollen
Invasion
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Invasion
Antibody
(IgE) Mast Cell
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Invasion
Pollen
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Invasion
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Invasion
Histamine
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What is Hay
fever?
Invasion
Crisis Human
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So we focused on the immune system.
To control hay fever…
It should control production of IgE and the histamine.
It should control production of B cell and Mast cell.
It should do suppress the helper T-cell
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抗原 抗原提示細胞
IL-12
NK cell
IFN-γ
Th1
Th2
IL-10
IFN-γ IL-2 TNF-β
IL-4 IL-10 IL-13
Cellular immunity
Humoral immunity
IL-10
IL-12 TNF-α
prime repression
T cell NK cell
macrophage
E0 B cell
Mast cell
allergen antigen
presenting cell
naïve T cell
An allergen invades
the body
Differentiateds in Th2.
Immune System
Invade
Produced
Stimulate
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IL-10
GFAP Hly D Hly B Tol C
GFAP IL-12 Hly A
STAT3
IL-10 receptor
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GFAP Hly D Hly B Tol C
GFAP IL-12 Hly A
P
P
P
STAT3+ P
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GFAP Hly D Hly B Tol C
GFAP IL-12 Hly A
P
P
P
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GFAP Hly D Hly B Tol C
GFAP IL-12 Hly A
P
P
P
IL-12
Exit Protein
Hly A
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GFAP Hly D Hly B Tol C
GFAP IL-12 Hly A
P
P
P
Exit Protein
Hly A
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1. Recepted IL10
・Two subunits consisting of α chain and β chain α chain: ligand binding subunit, and hight affinity. β chain: for signalization
IL10 repotor
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JAK
JAK
IL-10
IL-10 Receptor
Nucleus
outside
inside
GFAP
P P
P P
P P
STAT3
P
P
STAT3 + P
P
P
P
P
IL10 is received by the IL10 receptor ↓
The intracellular domain(JAK:Janus Kinase) of the receptor is phosphorylated. ↓
STAT3 is tyrosine phosphorylated. ↓
The process proceeds to the nucleus to form a dimer.
2. Phosphorylates STAT3
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3. Promoter and Downstream gene
Promoter is GFAP(Glial fibrillary acidic protein)gene.
There is the part where phosphoylated STAT3 binds to in GFAP
When phosphorylated STAT3 is combine GFAP IL12+HlyA and HlyB+HLyD+TolC of
downstream gene starts transcription.
HlyA is signal peptide.
HlyB+HlyD+TolC is membrane protein.
There is HlyB+HlyD to inner membrene,and
there is TolC to out membrene.
We produce IL12 with this structure.
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IL12 activity test is difficult in the short term, it was thought that instead of the GFP. It would be repleaced by IL12 if successful.
3. Promoter and Downstream gene
GFAP Hly D Hly B Tol C
GFAP GFP Hly A
P
P
P
GFP
Exit Protein
Hly A
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This time, we used the In-Fusion kit (purchased from Clontech) instead of restriction enzyme digestion and ligation.
Method
What is In-Fusion…
In-Fusion method is on the DNA recombinant method. The enzyme (In-Fusion
enzyme) recognize complement 15 base pair of both end of the DNA. The objective
gene is inserted into the Vector by the enzyme..
In-Fusion enzyme
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Method 1. IL10 receptor
α chain
We purchased DNA from Kazusa DNA Research Institute
Transformation
Colony PCR
In-
Fusion
Transformation
Colony PCR
We purchased DNA from Kazusa DNA Research Institute
Transformation
Colony PCR
β chain
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Method 2. STAT3
STAT3 plasmid was purchased from
Kazusa DNA Research Institute
Transformation
Colony PCR
In-Fusion
Transformation
Colony PCR
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Method 3. Downstream gene
GFP HlyA
From parts of iGEM
① ②
①
②
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Result 1.IL10 receptor
It was possible to clone DNA.
IL10 receptor α chain(1734bp) IL10 receptor β chain(975bp)
We succeeded cloning of IL-10 α and β chain DNA sequence with
attached the tag sequence for In-Fusion method.
However, We couldn’t construct the vector by the In-Fusion method.
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Result 2. STAT3
It was possible to clone DNA.
STAT3(2307bp)
We also succeeded cloning of STAT3 with attached the tag for In-
Fusion method.
However, We couldn’t construct the vector by the In-Fusion method.
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Result 3.Downstream gene
It was possible to clone DNA.
GFP (720bp) HlyA(187bp)
We succeed ed cloning of down stream gene with attached the tag
for In-Fusion method.
However, we also couldn’t construct the vector.
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Future Works
• To succeed In-Fusion method and to construct the vector for iGEM entry.
• Objective gene should be inserted to expression vector.
• To evaluate the activity of produced interleukin.
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“How do you think about gene recombination?”
It is adverse effects to a body. It might change ecosystem. It is untrustworthy. It is difficult.
1.Overview
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P1, P2, P3 level in the laboratory Cartagena Protocol
2.Posters
we made the poster about and explain these things in our iGEM project.
There is international decisions for nonproliferation of the gene recombination creature for the environment.
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Q1.What kind of impression did you have about genetic modification before hearing this explanation?
Q2.Were you interested in genetic modification?
3.Questionnaire
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Q1.Are you interested in genetic modification? Q5.Were you interested in genetic modification?
3.Questionnaire
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Thank you for listening!