Difference between revisions of "Part:BBa K4765001"

Revision as of 12:02, 1 October 2023

intimin _ contributed by Fudan iGEM 2023 _TOC__

Introduction

Intimin is a surface display system ,it was first described by Piñero-Lambea et. Al^[1]. and tested by iGEM22_GreatBay_SCIE. It includes a short N-terminal signal peptide to direct its trafficking to the periplasm, a LysM domain for peptidoglycan binding, and a 12-stranded beta-barrel for transmembrane insertion.

Usage and Biology

The protein attached to the C-terminus of intimin can achieve outer membrane localization. In our project, intimin is fused with antigens, nanobodies, and lectins, facilitating their display on the membrane of Escherichia coli. This approach allows for the binding of E. coli- E. coli and E. coli to cyanobacteria.

Characterization

Sequence and Features

Assembly Compatibility:

10
COMPATIBLE WITH RFC[10]
12
COMPATIBLE WITH RFC[12]
21
COMPATIBLE WITH RFC[21]
23
COMPATIBLE WITH RFC[23]
25
COMPATIBLE WITH RFC[25]
1000
INCOMPATIBLE WITH RFC[1000]
Illegal BsaI site found at 1244

Reference

↑ Piñero-Lambea, C., Bodelón, G., Fernández-Periáñez, R., Cuesta, A. M., Álvarez-Vallina, L., & Fernández, L. Á. (2015). Programming controlled adhesion of E. coli to target surfaces, cells, and tumors with synthetic adhesins. ACS Synthetic Biology, 4(4), 463–473. https://doi.org/10.1021/sb500252a

[1] Piñero-Lambea, C., Bodelón, G., Fernández-Periáñez, R., Cuesta, A. M., Álvarez-Vallina, L., & Fernández, L. Á. (2015). Programming controlled adhesion of E. coli to target surfaces, cells, and tumors with synthetic adhesins. ACS Synthetic Biology, 4(4), 463–473. https://doi.org/10.1021/sb500252a

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 ===Introduction===
 Intimin is a surface display system ,it was first described by Piñero-Lambea et. Al<ref>Piñero-Lambea, C., Bodelón, G., Fernández-Periáñez, R., Cuesta, A. M., Álvarez-Vallina, L., & Fernández, L. Á. (2015). Programming controlled adhesion of E. coli to target surfaces, cells, and tumors with synthetic adhesins. ACS Synthetic Biology, 4(4), 463–473. https://doi.org/10.1021/sb500252a</ref>. and tested by iGEM22_GreatBay_SCIE. It includes a short N-terminal signal peptide to direct its trafficking to the periplasm, a LysM domain for peptidoglycan binding, and a 12-stranded beta-barrel for transmembrane insertion.