Difference between revisions of "Part:BBa K3398003"

Revision as of 02:59, 22 October 2020

mamC_ZZ fusion protein

This part is encodes a fusion protein of mamC and ZZ. And for separation from other proteins at the purification step, we introduced a GST tag at the N-terminus and a thrombin site between the fusion protein and tag for cleavage after purification, which has been submitted as BBa_K3398004. To maximize the expression of a functional protein, we employed codon optimization to maximize the expression of a functional protein in Escherichia coli. Not only in E.coli, these parts can also be expressed by magnetotactic bacterium such as MSR-1 to produce magnetosomes modified with ZZ protein on the surface as a self-assembly platform for polymer varied antibodies.

Usage and Biology

MamC protein is a membrane protein which covers the most area of the magnetosome surface formed by magnetotactic bacteria MSR-1, and ZZ is the Fc-binding domain of staphylococcal protein A (SPA), an immunoglobulin-binding protein from the cell wall of Staphylococcus aureus. This fusion protein can be expressed and anchored onto the surface of magnetosomes by transferring the recombinant plasimd into MSR-1.The resulting recombinant magnetosomes will be capable of self-assembly with the Fc region of mammalian antibodies and will ve therefore useful for functionalization of magnetosomes such as being developed to a antibody vector or serving as specifically tumor-targeting contrast agents for MRI.

Characterization

Plasmid construction

We designed the fusion protein sequence ordered gene synthesis service from GenScript Biotech Corporation and obtained the recombinant pGEX-2TK plasmid with a GST tag. To confirm the sequence of the fusion protein, we designed a couple of primers to amplify the sequence by PCR and sent to Zhejiang Sunya Biotechnology Co., Ltd for sequencing.The vector map and PCR results are shown in Figure 1 and Figure 2 below.

Expression of mamC_ZZ

After the DNA sequence was confirmed (SUNYA, Zhejiang, CN), the pGEX-2TK construct was transformed into BL21 (DE3). The plasmid was transferred into E.coli BL21(DE3) and massively expressed after the addition of IPTG. To investigate the optimum concentration of IPTG and the optimum time for inducing, we carried out gradient experiments at the same time. The results of concentration and time gradient experiments are shown in Figure 3 and Figure 4 below, and it shows that the best concentration of IPTG for induing is 2mM and the optimum inducing time is 4 hour.

Sequence and Features