Difference between revisions of "Part:BBa K4390111"
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<partinfo>BBa_K4390111 short</partinfo> | <partinfo>BBa_K4390111 short</partinfo> | ||
| − | + | '''This part is not compatible with BioBrick RFC10 assembly but is compatible with the iGEM Type IIS Part standard [[Help:Standards/Assembly/Type_IIS|which is also accepted by iGEM.]]''' | |
| − | + | ==Usage and Biology== | |
| − | + | L2NC-linker is Part BBa_K3946002 but with the addition of a short linker (GSEGKSSGSGSESKST). L2NC is a truncated version of the L2 ribosomal protein from E. coli, designed for fusion to C-terminal of a protein using JUMP assembly. This tag contains just the N and C-terminal regions of L2 which were shown to have silica binding capacity in previous experiments, therefore allowing the use of a smaller tag without compromising on binding affinity. The attachment of L2NC-linker silica tag on the C-terminus of the functional enzyme would result in the 15.69 kDa increasement in weight. From literature, the dissociation constant between L2NC silica tag and silica beads is 1.7nM (Kim et al., 2020). | |
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| − | <span class='h3bb'>Sequence and Features</span> | + | |
| + | ==<span class='h3bb'>Sequence and Features</span>== | ||
<partinfo>BBa_K4390111 SequenceAndFeatures</partinfo> | <partinfo>BBa_K4390111 SequenceAndFeatures</partinfo> | ||
| + | ==Reference== | ||
| + | Kim S, Joo K, Jo B, Cha H. Stability-Controllable Self-Immobilization of Carbonic Anhydrase Fused with a Silica-Binding Tag onto Diatom Biosilica for Enzymatic CO2 Capture and Utilization. ACS Applied Materials & Interfaces. 2020;12(24):27055-27063. | ||
<!-- Uncomment this to enable Functional Parameter display | <!-- Uncomment this to enable Functional Parameter display | ||
Latest revision as of 13:26, 12 October 2022
L2NC-linker Silica tag (N-terminal)
This part is not compatible with BioBrick RFC10 assembly but is compatible with the iGEM Type IIS Part standard which is also accepted by iGEM.
Usage and Biology
L2NC-linker is Part BBa_K3946002 but with the addition of a short linker (GSEGKSSGSGSESKST). L2NC is a truncated version of the L2 ribosomal protein from E. coli, designed for fusion to C-terminal of a protein using JUMP assembly. This tag contains just the N and C-terminal regions of L2 which were shown to have silica binding capacity in previous experiments, therefore allowing the use of a smaller tag without compromising on binding affinity. The attachment of L2NC-linker silica tag on the C-terminus of the functional enzyme would result in the 15.69 kDa increasement in weight. From literature, the dissociation constant between L2NC silica tag and silica beads is 1.7nM (Kim et al., 2020).
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Reference
Kim S, Joo K, Jo B, Cha H. Stability-Controllable Self-Immobilization of Carbonic Anhydrase Fused with a Silica-Binding Tag onto Diatom Biosilica for Enzymatic CO2 Capture and Utilization. ACS Applied Materials & Interfaces. 2020;12(24):27055-27063.