Difference between revisions of "Part:BBa K3075000:Design"
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===Design=== | ===Design=== | ||
− | The following gene construct was designed to enable the cloning and expression of the recombinant | + | The following gene construct was designed to enable the cloning and expression of the recombinant protein PAM-SnoopT-His within a T7 expression system. |
Additions to the gene are as follows: | Additions to the gene are as follows: | ||
− | |||
− | :*Hexahistidine peptide tag – high affinity to Ni2+ - enables protein purification using Immobilised metal affinity chromatography (IMAC) via a Ni-NTA column. | + | :*'''Gibson forward and reverse overhangs''' – complementary overhangs outside the protein coding region enable cloning into pET19b plasmid via Gibson Assembly. |
+ | |||
+ | :*'''Hexahistidine peptide tag''' – high affinity to Ni2+ - enables protein purification using Immobilised metal affinity chromatography (IMAC) via a Ni-NTA column. | ||
+ | |||
Additionally, GSG linkers are included between the peptide sequences. This results in improved fluidity, allowing individual unhindered protein folding of each component (enzyme and tag system). | Additionally, GSG linkers are included between the peptide sequences. This results in improved fluidity, allowing individual unhindered protein folding of each component (enzyme and tag system). | ||
− | |||
− | Figure 1: Sequence annotation of the designed gene constructs for a visual representation of the spatial arrangement of PAM-SnoopT | + | [[File:PAM_anottated.png]] |
+ | |||
+ | |||
+ | '''Figure 1:''' Sequence annotation of the designed gene constructs for a visual representation of the spatial arrangement of PAM-SnoopT-His gene construct. Image by Linda Chen. | ||
===Source=== | ===Source=== | ||
Originated from ''Taxus wallichiana var. chinensis'' | Originated from ''Taxus wallichiana var. chinensis'' |
Latest revision as of 00:42, 22 October 2019
PAM-SnoopT-His
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 498
- 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 498
- 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 498
Illegal BamHI site found at 2131 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 498
- 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 498
Illegal NgoMIV site found at 393 - 1000COMPATIBLE WITH RFC[1000]
Design
The following gene construct was designed to enable the cloning and expression of the recombinant protein PAM-SnoopT-His within a T7 expression system.
Additions to the gene are as follows:
- Gibson forward and reverse overhangs – complementary overhangs outside the protein coding region enable cloning into pET19b plasmid via Gibson Assembly.
- Hexahistidine peptide tag – high affinity to Ni2+ - enables protein purification using Immobilised metal affinity chromatography (IMAC) via a Ni-NTA column.
Additionally, GSG linkers are included between the peptide sequences. This results in improved fluidity, allowing individual unhindered protein folding of each component (enzyme and tag system).
Figure 1: Sequence annotation of the designed gene constructs for a visual representation of the spatial arrangement of PAM-SnoopT-His gene construct. Image by Linda Chen.
Source
Originated from Taxus wallichiana var. chinensis