Biomod/2012/TeamSendaiA/Results & Discussion

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Team Sendai Top



selecotor electorophoresis

constant voltage: 50V
temperature: 4℃(in refrigerater)
time: 2 hours
SYBR Gold as a stain for 10 minutes
1X TAE added to Mg2+ as a buffer
1 Target
2 Selector1
3 Selector2
4 Selector3
5 Target + Selector1
6 (Target + Selector1)+Selector2
7 (Target + Selector1 + Selector2 + Selector3
8 Target + Selector2
9 Target + Selector3
10 Marker

[Target is passed between Selectors]
In a fridge (at 4 degree)
1. hybridize the target and Selector1
Put a target and Selector1 together and leave it for 時間
2. pass the target from Selector1 to Selector2
After hybridizing the target and Selector1, add Selector2 and leave it for 時間
3. pass the target from Selector2 to Selector3
After hybridizing the target and Selector2, add Selector3 and leave it for 時間

If Selector binds to a target, its band is seen upper, and the left target is observed weakly.
Selector1 binds to the target (lane画像を付けて、レーンの名前). Selector1 releases the target and Selector2 catches it (laneレーン名, single stranded Selector1, and Selector2 with the target). Then Selector2 releases the target and Selector3 catches it (laneレーン名, single stranded Selector1and 2, and Selector3 with the target). Therefore, we successfully showed that the target is passed between Selectors.

[Selector in the gate catches the target]
1. prepare three kinds of gates. Gate with no selector, gate with selector2, and gate with selector1 and 2.
2. put each gate and a target together.

With no selector in the gate, a target doesn’t goes in the gate(写真、laneレーンの名前). With selector2, or selector1 and 2 in the gate, a target goes into the gate (laneレーンの名前). The efficiency is the best when two selectors are planted in the gate. Thus, we concluded that selector in the gate greatly contributes to catch the target.




We use fluorescein to confirm that the tube insert into the liposome. For example, We put Lucifer Yellow fluorescein into big liposome and made​ a hole using the α- Hemorijin into liposomes. Then, we observed that fluorescein was flowing out from it. Alpha-hemolysin is toxin which makes a hole in the cell and is often used in experiments liposome system. The way of the experience of the protein α-hemolysin was dissolved in 150mM KCL, 10 mM HPES and kept at 4℃ for up to 6 months. And 0.6 μL of 1 mg/mL α-hemolysin solution was added directly to a 6 μL sample on the microscope slide. The figure shows that fluorescein flowing out from a liposome. Therefore, we are sure that observing fluorescein would be a confirmatory experiment which our tube stuck to the liposome or not.
(リポソームに筒が刺さっているかどうかを確かめるために、蛍光分子を使用する。実験として、ルシファーイエロー(染色液)を大きなリポソームに入れて、リポソームにαヘモリジンを使用して穴を開け、リポソームから蛍光分子が流れ出てくるところを観察した。αヘモリジンは、細胞に穴を開ける毒素の一つで、リポソーム系の実験でよく使われている。実験結果としては、写真の通り観察できたので、筒がリポソームに刺さったかどうかを確かめる方法として使用できることが分かった。ネガコンの写真 ポジコンの写真)
We also can confirm that by adding hoechst to the sample, the tube is on the membrane of liposome or not, and confirm that fluorescein does not leak from the hole in nature.
We examined the appropriate composition of the liposome. And we decided the composition; DOPC : DSPE-PEG2000 : Fructose = 100:1:1000.
(リポソームの適切な組成を調べ、DOPC:DSPE-PEG2000:Fructose = 100:1:1000 という組成に決めた。)
Lipids 0.4mM
Inside of the liposome is constituted Lucifer yellow(3-dihydro-1,3-dioxo-1H-benz(de) isoquinoline-5,8- disulfonate dilithium 6-amino-2-((hydrazinocarbonyl)amino)-2)
(DNAをヘキスト染色。穴が開いていればLYが外に漏れだすはず ポジコンの実験プロトコルも書く

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