Difference between revisions of "Part:BBa K4586014"
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We implemented this part in our design to form our loading system for the therapeutic agent to be loaded into exosomes. This loading system is composed of three elements: First, CD63, which is a transmembrane protein naturally present and highly expressed on the external surface of the exosome membrane, second L7Ae, which is a RNA-binding protein conjugated to the internal domain of the CD63 protein, in order to bind to the third element of the loading system present in the 3` end of our cargo, which is the C\D box or kink turn as shown in figure 1. and figure 2. | We implemented this part in our design to form our loading system for the therapeutic agent to be loaded into exosomes. This loading system is composed of three elements: First, CD63, which is a transmembrane protein naturally present and highly expressed on the external surface of the exosome membrane, second L7Ae, which is a RNA-binding protein conjugated to the internal domain of the CD63 protein, in order to bind to the third element of the loading system present in the 3` end of our cargo, which is the C\D box or kink turn as shown in figure 1. and figure 2. | ||
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Revision as of 14:01, 22 September 2023
CD63
Part Description
This part is the cell surface protein, which is a member of the tetraspanin family. It has numerous functions, such as being a marker for multivesicular bodies, quantifying extracellular vesicles, and can also be fused with other proteins to combine functional devices in the exosomal membrane.
Usage
We implemented this part in our design to form our loading system for the therapeutic agent to be loaded into exosomes. This loading system is composed of three elements: First, CD63, which is a transmembrane protein naturally present and highly expressed on the external surface of the exosome membrane, second L7Ae, which is a RNA-binding protein conjugated to the internal domain of the CD63 protein, in order to bind to the third element of the loading system present in the 3` end of our cargo, which is the C\D box or kink turn as shown in figure 1. and figure 2.
Figure 1: This figure illustrates the mechanism of loading our therapeutic agent in the form of mRNA selectively and efficiently into our engineered exosomes secreted form the MSCs,this loading is done through labeling the gene of interest with C\D box a hairpin structure IN THE 3` end this box have high affinity to the RNA binding protein L7Ae that is expressed on the internal surface of the engineered exosomes membrane conjugated to his tagged CD63 protein that is a natural highly expressed transmembrane protein within the exosomes.
Figure 2: This figure shows the design of the biological circuit expressing our loading system on the exosomes membrane ,this system consists of two main component ,First the RNA binding protein L7Ae conjugated to the second component, which is CD3 a transmembrane protein that is naturally expressed on the exosomes membrane.
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]