Difference between revisions of "Part:BBa K3117024:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | ... | + | Our flexible linker is composed of small, non-polar (e.g. Gly) and polar (e.g. Ser or Thr) amino acids. By adjusting the copy number, in this case 4 repeats of GGGGS, the length of this GS linker can be optimized to achieve appropriate separation of the proteins of interest [1]. 3 repeats ensure a high level of flexibility. |
− | + | ||
===Source=== | ===Source=== | ||
− | + | This part comes from genomic DNA. | |
===References=== | ===References=== | ||
+ | |||
+ | [1]: Chen, Xiaoying; Zaro, Jennica L.; Shen, Wei-Chiang (2013): Fusion protein linkers: property, design and functionality. In: Advanced drug delivery reviews 65 |
Latest revision as of 10:45, 21 October 2019
(Glycine)x4-Serine Linker
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
Our flexible linker is composed of small, non-polar (e.g. Gly) and polar (e.g. Ser or Thr) amino acids. By adjusting the copy number, in this case 4 repeats of GGGGS, the length of this GS linker can be optimized to achieve appropriate separation of the proteins of interest [1]. 3 repeats ensure a high level of flexibility.
Source
This part comes from genomic DNA.
References
[1]: Chen, Xiaoying; Zaro, Jennica L.; Shen, Wei-Chiang (2013): Fusion protein linkers: property, design and functionality. In: Advanced drug delivery reviews 65