Protocol: Difference between revisions
| Line 64: | Line 64: | ||
=== 6. 使用 10 kDa 超滤管超滤去除游离 DBCO === | === 6. 使用 10 kDa 超滤管超滤去除游离 DBCO === | ||
=== 7. Oligo === | |||
{| class="wikitable" style="text-align:center; width:90%" | |||
! Name !! 序列 !! bp !! 修饰 !! Nmol/管 !! Abuffer (μL) !! 浓度 (mM) | |||
|- | |||
| S1 || CTCTCCTTCTTCCCTTTC TTT || 21 || 5'Azide || 123.53 || 123.53 || 1 | |||
|- | |||
| S2 || TTCGAGACGATGAACATCAGC || 21 || 5'Azide || 97.51 || 97.51 || 1 | |||
|} | |||
=== 7. 加入 Oligo,并在 37 ℃ 下孵育 4 h === | === 7. 加入 Oligo,并在 37 ℃ 下孵育 4 h === | ||
Revision as of 05:19, 1 November 2025
Protein(RuCHMO/GDH) Conjugation to DNA Origami
Methods
Conjugation
- Proteins containing 6x Histidine at the C terminus reacted, with the chemical DBCO-PEG4-Bis-sulfone(DPBS) for 4 h at room temperature. The bis-sulfone group reacts with the Histidines at the C terminus of the protein, and then an azide modified oligonucleotide is conjugated to the protein by click chemistry between the azide- and the DBCO-group.
Incubation
- conjugation: DNA Origami = 20:1, and incubate in a PCR machine with a temperature ramp starting from 1 h at 37 ℃ follow by 14 h at 22 ℃, and immediately after incubation the nanopatterns are stored at 4 ℃.
Oligonucleotide Sequence
- sequence(RuCHMO):CTCTCCTTCTTCCCTTTCTTT
- Sequence(GDH):TTCGACAGCATGAACATCAGC
Protein
- RuCHMO: 65.45 KDa
- GDH: 35 KDa
Purification
- 30 kDa MWCO 0.5 ml Amicon centrifugal filters (Milli-pore)
electro-phoresis
| Reagent | Sequence |
|---|---|
| DBCO-PEG4-Bis-sulfone | |
| azide modified oligonucleotide | CTCTCCTTCTTCCCTTTCTTT |
| azide modified oligonucleotide | TTCGACAGCATGAACATCAGC |
Protocol (版本 1.0)
1. GDH 制备
取 1.4 mg GDH 溶解于 2 mL 1×PBS 中。
2. 稀释 GDH(样品液)
| 样品 | 原样品浓度 | 终样品浓度 | 加入量 | 总体积 |
|---|---|---|---|---|
| GDH | 0.7 mg/mL | 0.175 mg/mL | 25 μL | 100 μL |
3. 溶解 DBCO-PEG4-Bis-Sulfone 于 DMF(N,N-二甲基甲酰胺) 中(100 mM)
取 DBCO 2 mg 溶解DMF 20 ul 中
4. 稀释 DBCO(样品液)
| 样品 | 原样品浓度 | 终样品浓度 | 加入量 | 总体积 |
|---|---|---|---|---|
| DBCO | 100 mM | 20 mM | 2 μL | 10 μL |
5. 向 GDH 样品液中加入 DBCO,并在室温下孵育 4 h
| 样品 | 最终浓度 | 分子量 | 总摩尔量 | Eq DBCO | DBCO 摩尔量 | DBCO 加入量 | 总体积 |
|---|---|---|---|---|---|---|---|
| GDH | 5 mM | 35 kDa | 0.5 nMol | 20 Eq | 10 nMol | 0.5 μL | 100 μL |
6. 使用 10 kDa 超滤管超滤去除游离 DBCO
7. Oligo
| Name | 序列 | bp | 修饰 | Nmol/管 | Abuffer (μL) | 浓度 (mM) |
|---|---|---|---|---|---|---|
| S1 | CTCTCCTTCTTCCCTTTC TTT | 21 | 5'Azide | 123.53 | 123.53 | 1 |
| S2 | TTCGAGACGATGAACATCAGC | 21 | 5'Azide | 97.51 | 97.51 | 1 |
7. 加入 Oligo,并在 37 ℃ 下孵育 4 h
| 样品 | 总摩尔量 | Eq Oligo | Oligo 摩尔量 | Oligo 加入量 | 总体积 |
|---|---|---|---|---|---|
| GDH | 0.5 nMol | 20 Eq | 10 nMol | 10 μL | 100 μL |
8. 凝胶电泳
等量的 GDH , 偶联产物 和 Marker 跑胶,对蛋白进行考马斯亮蓝染色比对。