Difference between revisions of "Part:BBa K1985011"

Latest revision as of 15:43, 27 October 2016

Sequence coding for amyloid Sup35 residues 1-61 and Cytochrome b562

This part is an improved version of a previously designed BioBrick (Part:BBa_K1739003) designed by the Kent 2015 iGEM team. It contains three segments, the CsgA signal sequence, the first 61 aminoacids of the prion domain Sup35 and the electron transfer protein cytochrome 562. Our improved BioBrick aims to optimize the self-assembly process of amyloid fibrils with the addition of these residues as they have been considered to be a suitable building block for the assembly of functional nanostructures[1]. This improved plasmid does not contain the constitutive promoter (Part:BBa_J23104) as was used for (Part:BBa_K1739003), giving the user choice over the promoter that they use.

Sequence and Features

Validation

The plasmid was analysed through a diagnostic double restriction cut, using the enzymes NdeI and SspI. This was followed by agarose gel electrophoresis. The enzymes cleave the insert and a part of the plasmid at 1966bp, with the remainder plasmid being 790 bp. The sizes of the two fragments were compared with the size of the Invitrogen 1kB DNA marker and was found that our fragments were the correct sizes.

Figure 1.1% agarose gel of the restriction digest of BBa_K1985011 in pSB1C3 plasmid backbone with NdeI and SspI. Single digest with NdeI shows undigested plasmid as two bands are seen

Function validation was performed on (Part:BBa_K1985014) by diagnostic Congo Red plate assay and AFM imaging that demonstrated the presence of amyloid by formation of red colonies.

References

[1] Men, D., Zhou, J., Li, W., Leng, Y., Chen, X., Tao, S., and Zhang, X. "Fluorescent protein nanowire-mediated protein microarrays for multiplexed and highly sensitive pathogen detection". ACS Appl. Mater. Interfaces (June 2016) DOI: 10.102.