| 查看: 741 | 回复: 6 | |||
| 当前主题已经存档。 | |||
xiangao金虫 (正式写手)
|
[交流]
融合基因
|
||
|
我现在想构建一个融合蛋白基因并且得到表达,刚接触以前没做过,请高手指点一下,需要什么注意事项? 听说两个融合基因之间有个linker,是这样吗?直接overlap,去掉前一个基因的终止密码子,和后基因的起始密码子,可以吗? 还有什么注意的啊? [ Last edited by xiangao on 2009-9-29 at 20:52 ] |
» 猜你喜欢
售SCI-T0P文章,我:8O.5.5.1.O.54,科目齐全,可+急
已经有4人回复
售SCI文章,我:8O.5.5.1O.54,科目全,可十急
已经有5人回复
售SCI一区T0P文章,我:8.O55.1.O.54,科目全,可十急
已经有5人回复
售SCI文章,我:8O5.5.1.O.54,科目齐全,可+急
已经有6人回复
售SCI一区T0P文章,我:8.O55.1.O.54,科目全,可十急
已经有4人回复
售SCI文章,我:8O5.5.1.O.54,科目齐全,可+急
已经有4人回复
小木虫上这么多卖论文的,真有人买论文么?感觉没必要啊
已经有12人回复
售SCI一区文章,我:8O5.5.1.O5.4,科目全,可伽急
已经有4人回复
各位道友,我要去昆明玩几天,回来见。
已经有8人回复
售SCI一区T0P文章,我:8O.55.1.O.5.4,科目齐全,可+急
已经有4人回复
xiangao
金虫 (正式写手)
- 应助: 4 (幼儿园)
- 金币: 1375.1
- 散金: 268
- 红花: 2
- 帖子: 434
- 在线: 310.9小时
- 虫号: 679064
- 注册: 2008-12-21
- 性别: GG
- 专业: 生物化工与食品化工
2楼2009-09-29 21:55:15
mascotte
金虫 (正式写手)
- BioEPI: 2
- 应助: 10 (幼儿园)
- 金币: 1998.9
- 红花: 3
- 帖子: 328
- 在线: 193.4小时
- 虫号: 492008
- 注册: 2008-01-07
- 专业: 生物化学
★ ★ ★ ★ ★ ★ ★ ★
amisking(金币+3,VIP+0):我觉得中文比较容易让人看懂! 9-30 08:27
xiangao(金币+5,VIP+0):it's very useful,thank you 9-30 09:36
amisking(金币+3,VIP+0):我觉得中文比较容易让人看懂! 9-30 08:27
xiangao(金币+5,VIP+0):it's very useful,thank you 9-30 09:36
|
In your design, have you thought about including a protease site to remove the tag if necessary? By doing this, you also add a little spacer between your protein. If possible, I was taught to remove the Met for N-terminal fusions, as internal Met are usually rare. I usually just remove the Met and start the coding sequence of protein with the second amino acid, I do not replace the Met with another amino acid. I don't think the addition of one amino acid is going to change things. I mean, is there any real difference between the last amino acid of your tag and a residue added to replace the Met? If you are set on adding an amino acid, I would choose something neutral, like alanine or possibly valine (glycine or leucine could work as well). It should be noted, in bacteria, Val (GTG) can act as a start codon. I'm not sure proline would be good, since it is not very flexible and can cause kinks in the protein structure. For larger fusions, for example GFP, I have seen people make flexible spacers consisting of Ser/Thr-Gly repeats. I believe it looks something like S-G-G-G-G-S. You can add these units in tandem for larger spacers if needed. Finally, you can always look at commercial expression vectors to see the kinds of amino acids they use as spacers between different elements. [ Last edited by mascotte on 2009-9-30 at 08:04 ] |
3楼2009-09-30 07:29:32
bioxixi
木虫 (著名写手)
- 应助: 2 (幼儿园)
- 金币: 2254.6
- 散金: 55
- 红花: 1
- 帖子: 1080
- 在线: 89.5小时
- 虫号: 662656
- 注册: 2008-11-26
- 性别: MM
- 专业: 细胞生物学
4楼2009-09-30 08:19:30
xiangao
金虫 (正式写手)
- 应助: 4 (幼儿园)
- 金币: 1375.1
- 散金: 268
- 红花: 2
- 帖子: 434
- 在线: 310.9小时
- 虫号: 679064
- 注册: 2008-12-21
- 性别: GG
- 专业: 生物化工与食品化工
|
thank you for your reply.I wonder if a cut is not necessary between the tag and target protein, can I get an active protein? It is said most of the fusion protein is deactive,maybe because the former protein repress or hinder the active site where the substrate and enzyme react can you recommend some related papers or literature about this work to me? wish your guide! |
5楼2009-09-30 10:22:04
mascotte
金虫 (正式写手)
- BioEPI: 2
- 应助: 10 (幼儿园)
- 金币: 1998.9
- 红花: 3
- 帖子: 328
- 在线: 193.4小时
- 虫号: 492008
- 注册: 2008-01-07
- 专业: 生物化学
6楼2009-09-30 22:40:49
7楼2009-09-30 22:55:50










回复此楼