Difference between revisions of "Part:BBa K4016026"

Revision as of 16:09, 21 October 2021

zdk-GFPnano

This composite part is designed to target GFP with Part:BBa_K4016025 through aslov2-zdk1 interaction and GFP-GFPnano. With this composite part, zdk1 and GFPnano can be expressed in cells, and GFPnano was added to C-terminal of zdk1.

Usage and Biology

In order to realize the assembly of the light control module, our team connected one basic part in light control module , zdk1, with GFPnano, using the separation of aslov2-zdk1 under blue light and the combination in the dark, thereby indirectly through GFP fluorescence brightness to verify whether aslov2-zdk1 works.

LOV2 trap and release of protein (LOVTRAP), an optogenetic approach capable of repeatedly and reversibly controlling protein activity with precise kinetics. This approach uses a small protein, which we named Zdark (Zdk1), generated by mRNA display screening of a library derived from the Z subunit of protein A. Zdk1 binds selectively to the dark state of LOV2[1]. Zdk1 is a kind of protein which can bind with lov2 induced by blue light.

GFPnano is the nanobody of GFP, a green fluorescent protein, which can be observed easily. This part could target GFP and bind TRIM21-aslov2 thought the aslov2-zdk1 interaction and lead to the degradation induced by ubiquitin-proteasome.

The PRYSPRY-lgG Fc interaction of (Part:BBa_K2653016) is replaced with aslov2-zdk1 interaction to realize controlling of both initiation and rate of the degradation. Zdk1 and aslov2 are proteins which separate from each other under induction of blue light. By providing dark environment, aslov2-zdk1 dimerization would trigger the formation of EGFP-GFPnano-truncated_Trim21 trimer, in which the truncated Trim21 would mediate the ubiquitylation and degradation of EGFP protein.

Figure 1. Schematic figure of BBa_K4016026 and BBa_K4016025

Here is the mechanism of the recombined zdk1-GFPnano:

1. zdk1-GFPnano dissociate with HA-Trim21-aslov2 by the dissociation of zdk1-aslov2 under the light, and in the dark they connect together to work.

2. GFPnano binds with GFP, and target GFP.

Characterization

This part is validated through 4 experiments: PCR, enzyme digestion, sequencing and functional test.

PCR

The PCR is performed with 2 x Phanta Max Master Mix.

F-Prime: 5’-CTAGCGTTTAAACTTAAGCTTGCCACCATG-3’

R-Prime: 5’-TGGATATCTGCAGAATTCTTAtgaggagacggtgacctggg-3’

The PCR protocol is selected based on the Users Manuel. The Electrophoresis was performed on a 1％ Agarose glu.

Enzyme Digestion

After the assembly the plasmid was transferred into the Competent E. coli DH5α). After culturing overnight in LB,we minipreped the plasmid for cutting. The cutting procedure was performed with Hind III EcoR I restriction endonuclease bought. The plasmid was cutted in a 20μL system at 37 ℃ for 2 hours. The Electrophoresis was performed on a 1％ Agarose glu.

Sequecing

The plasmid was sequenced correct.

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 227

Functional test

This part (BBa_K4016026) was tested together with HA-Trim21-aslov2 (Part:BBa_K4016025).

Method

Florescent imaging:

To validate the function of our system(Trim21-aslov2-zdk1-GFPnano), HEK-293T cells were co-transfected with GFP expressing reporter plasmids and our system expressing plasmids as the experimental group (plasmids: with the parts of Trim21-aslov2 and zdk1-GFPnano). HEK-293T cells were co-transfected with GFP expressing reporter plasmids, the cells were divided into two groups. One was provided with blue light for 24 hours and the other was in the dark at the same time(control group). Florescent imaging showed that the different results of GFP fluorescence between our system and control group.

Result

Florescent imaging showed that comparing to the control group in which HEK-293T cells were co-transfected with GFP expressing reporter plasmid and our designed plasmid and were put in the dark, GFP fluorescence in blue light group was higher than the control group. This confirmed that our system stopped the degradation of GFP under blue light, thus verifying the effectiveness of our design.

Figure 2. Fluorescence images and intensity quantification of BBa_K4016025 and BBa_K4016026 transfected group and they were divided into different conditions, in dark and under blue light for 24hours. HEK-293T cells were transfected with GFP-expression plasmid.

Reference

[1] Hui Wang,Klaus M. Hahn. LOVTRAP: A Versatile Method to Control Protein Function with Light[J]. Current Protocols in Cell Biology,2016,73(1):

@@ Line 69: / Line 69: @@
 ===Method===
-*1. Florescent imaging:
+* Florescent imaging:
 To validate the function of our system(Trim21-aslov2-zdk1-GFPnano), HEK-293T cells were co-transfected with GFP expressing reporter plasmids and our system expressing plasmids as the experimental group (plasmids: with the parts of Trim21-aslov2 and zdk1-GFPnano). HEK-293T cells were co-transfected with GFP expressing reporter plasmids, the cells were divided into two groups. One was provided with blue light for 24 hours and the other was in the dark at the same time(control group). Florescent imaging showed that the different results of GFP fluorescence between our system and control group.