Difference between revisions of "Part:BBa K1638035:Design"
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===Source=== | ===Source=== | ||
− | + | pUT18C | |
− | + | <br> | |
+ | Human thioredoxin sequence: UniProt (AC: P10599) | ||
+ | <br> | ||
+ | Intein sequence: pTYB21 (IMPACT kit) | ||
===References=== | ===References=== |
Revision as of 09:58, 18 September 2015
hTrx-based scaffold fused to T18 through intein and a flexible linker
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 1563
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 1229
Illegal BamHI site found at 711
Illegal XhoI site found at 2374 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 252
Illegal NgoMIV site found at 662
Illegal NgoMIV site found at 2106
Illegal AgeI site found at 468 - 1000COMPATIBLE WITH RFC[1000]
Design Notes
A fragment of this part (linker_intein_scaffold) was synthesized by IDT as a gBlock gene fragment. This gene fragment was suffixed to the T18 domain of cyaA from Bordetella pertussis by digesting the two parts with BamHI and PstI followed by ligation.
Library
- Choose the size of your library. Typically the length of the variable peptide loop is between 10 and 20 amino acids.
- Dependent on the size your variable peptide loop, you can for example contruct the library as following: ATATGCGCTCGAG(NNK)xGAGCTCATTACCG (where N represent A, T, G or C and K represent G or C). The NNK codon minimizes the number of stop codons. The XhoI restriction included allows insertion of library into the scaffold.
- Order the library as duplex-DNA
- When delivered, cut the library and scaffold with XhoI restriction enzyme and ligate.
Important note: This part cannot be used in the standard backbones pSB1C3 or pSB1K3, as they include a xhoI restriction site. Instead we recommend using the pSB1A2 backbone
Source
pUT18C
Human thioredoxin sequence: UniProt (AC: P10599)
Intein sequence: pTYB21 (IMPACT kit)