Difference between revisions of "Part:BBa K5301017"

Revision as of 14:58, 1 October 2024

sGFP1-10 tether is composed of mSA, a 3C linker, a 6His tag, and sGFP 1-10.

sGFP1-10 tether is composed of mSA (BBa_K4623001), a 3C linker, a 6×His tag, and sGFP 1-10 (No part name specified with partinfo tag.).We construct membrane protein dimers through the interaction between biotin and streptavidin, as well as the self-assembly mechanism of sGFP.

Figure 1.AlphaFold2 predition of the sGFP1-10 tether.

Usage and Biology

mSA is used for binding to biotinylated proteins, and sGFP1-10 and sGFP11 self-assemble to form GFP, thereby creating a protein dimer that can report the outcome with fluorescence.

Characterization

PCR

We conducted colony PCR validation to assess the feasibility of the plasmid pathway, as shown in Figure 2, where the corresponding bands are very clear, indicating that the target fragments were successfully introduced into the plasmid and transformed into the bacterial strain.

Figure 2.PCR result of the sGFP1-10 tether.The base sequence length of the sGFP1-10 tether is 1071 base pairs (bp)

SDS-PAGE

SDS-PAGE was used to verify the purification of the sGFP1-10 tether. Due to the particularity of mSA, we simultaneously purified the soluble proteins from the supernatant and the inclusion body proteins from the pellet after bacterial lysis. It was observed that the concentration and purity of the purified inclusion body proteins were high, while the concentration of the soluble proteins was low. Further exploration of soluble protein expression or assessment of inclusion body protein activity could be conducted subsequently.

Figure 3.SDS-PAGE of the soluble sGFP1-10 tether.The molecular weight of the sGFP1-10 tether is 39.2kDa.

Figure 4.SDS-PAGE of the inclusion body sGFP1-10 tether.The molecular weight of the sGFP1-10 tether is 39.2kDa.

ELISA

We conducted an activity analysis of sGFP tethers. Using the standard interaction between streptavidin and biotin as a control, we observed the interaction between the expressed protein and biotin to determine the activity of the expressed sGFP tether. Observations from Figure 4 indicated that the directly purified soluble sGFP1-10 tether exhibited some activity, while the inclusion body proteins, after purification through denaturation and refolding, didn't exhibit activity.

Figure 1.ELISA of the sGFP1-10 tether. Row A, wells 1-9 contain a gradient of mSA standard solutions, while wells 10 and 11 are negative controls with 0.5% BSA. Row B, wells 1-10 also contain a gradient of mSA standard solutions, and wells 11 and 12 are negative controls with 0.5% BSA. Row C, wells 1 and 4 are refolded samples of sGFP1-10 tether protein. Row D, well 1 contains purified samples of sGFP1-10 tether protein. Rows E and F, well 2 contains purified inclusion body samples of sGFP1-10 tether.

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
INCOMPATIBLE WITH RFC[25]
Illegal AgeI site found at 82
Illegal AgeI site found at 142
1000
COMPATIBLE WITH RFC[1000]

@@ Line 3: / Line 3: @@
 <partinfo>BBa_K5301017 short</partinfo>
-sGFP1-10 tether is composed of mSA, a 3C linker, a 6×His tag, and sGFP 1-10.We construct membrane protein dimers through the interaction between biotin and streptavidin, as well as the self-assembly mechanism of sGFP.
+sGFP1-10 tether is composed of mSA (<partinfo>BBa_K4623001</partinfo>), a 3C linker, a 6×His tag, and sGFP 1-10 (<partinfo>BBa_ K5301012</partinfo>).We construct membrane protein dimers through the interaction between biotin and streptavidin, as well as the self-assembly mechanism of sGFP.
+<div class="center"><div class="thumb tnone"><div class="thumbinner" style="width:min-content;"><div style="zoom:0.2;overflow:hidden;">
+https://static.igem.wiki/teams/5301/parts/sgfp1-10-tether-structure.png
+</div><div class="thumbcaption">
+Figure 1.AlphaFold2 predition of the sGFP1-10 tether.
+</div></div></div></div>
 ===Usage and Biology===
@@ Line 11: / Line 17: @@
 ===Characterization===
 ==PCR==
-We conducted colony PCR validation to assess the feasibility of the plasmid pathway, as shown in Figure 1, where the corresponding bands are very clear, indicating that the target fragments were successfully introduced into the plasmid and transformed into the bacterial strain.
+We conducted colony PCR validation to assess the feasibility of the plasmid pathway, as shown in Figure 2, where the corresponding bands are very clear, indicating that the target fragments were successfully introduced into the plasmid and transformed into the bacterial strain.
 <div class="center"><div class="thumb tnone"><div class="thumbinner" style="width:min-content;"><div style="zoom:0.6;overflow:hidden;">
 https://static.igem.wiki/teams/5301/parts/sgfp1-10-pcr.png
 </div><div class="thumbcaption">
-Figure 1.PCR result of the sGFP1-10 tether.The base sequence length of the sGFP1-10 tether is 1071 base pairs (bp)
+Figure 2.PCR result of the sGFP1-10 tether.The base sequence length of the sGFP1-10 tether is 1071 base pairs (bp)
 </div></div></div></div>
 ==SDS-PAGE==
-SDS-PAGE was used to verify the purification of the sGFP1-10 tether. Due to the particularity of mSA, we simultaneously purified the soluble proteins from the supernatant and the inclusion body proteins from the pellet after bacterial lysis. It can be observed that the concentration and purity of the purified inclusion body proteins are high, while the concentration of the soluble proteins is low. Further exploration of soluble protein expression or assessment of inclusion body protein activity can be conducted subsequently.
+SDS-PAGE was used to verify the purification of the sGFP1-10 tether. Due to the particularity of mSA, we simultaneously purified the soluble proteins from the supernatant and the inclusion body proteins from the pellet after bacterial lysis. It was observed that the concentration and purity of the purified inclusion body proteins were high, while the concentration of the soluble proteins was low. Further exploration of soluble protein expression or assessment of inclusion body protein activity could be conducted subsequently.
 <div class="center"><div class="thumb tnone"><div class="thumbinner" style="width:min-content;"><div style="zoom:0.4;overflow:hidden;">
 https://static.igem.wiki/teams/5301/parts/sgfp1-10-protein.png
 </div><div class="thumbcaption">
-Figure 2.SDS-PAGE of the soluble sGFP1-10 tether.The molecular weight of the sGFP1-10 tether is 39.2kDa.
+Figure 3.SDS-PAGE of the soluble sGFP1-10 tether.The molecular weight of the sGFP1-10 tether is 39.2kDa.
 </div></div></div></div>
@@ Line 31: / Line 37: @@
 https://static.igem.wiki/teams/5301/parts/sgfp1-10-inclusion-body.png
 </div><div class="thumbcaption">
-Figure 3.SDS-PAGE of the inclusion body sGFP1-10 tether.The molecular weight of the sGFP1-10 tether is 39.2kDa.
+Figure 4.SDS-PAGE of the inclusion body sGFP1-10 tether.The molecular weight of the sGFP1-10 tether is 39.2kDa.
 </div></div></div></div>
 ==ELISA==
-We conducted an activity analysis of sGFP tethers. Using the standard interaction between streptavidin and biotin as a control, we observed the interaction between the expressed protein and biotin to determine the activity of the expressed sGFP tether. Observations from Figure 1 indicate that the directly purified soluble sGFP tether exhibits some activity, while the inclusion body proteins, after purification through denaturation and refolding, do not exhibit activity.
+We conducted an activity analysis of sGFP tethers. Using the standard interaction between streptavidin and biotin as a control, we observed the interaction between the expressed protein and biotin to determine the activity of the expressed sGFP tether. Observations from Figure 4 indicated that the directly purified soluble sGFP1-10 tether exhibited some activity, while the inclusion body proteins, after purification through denaturation and refolding, didn't exhibit activity.
 <div class="center"><div class="thumb tnone"><div class="thumbinner" style="width:min-content;"><div style="zoom:1.0;overflow:hidden;">
 https://static.igem.wiki/teams/5301/parts/elisa.png
 </div><div class="thumbcaption">
-Figure 1.ELISA of the expressed mSA(present in the form of sGFP tether).
+Figure 1.ELISA of the sGFP1-10 tether.
 Row A, wells 1-9 contain a gradient of mSA standard solutions, while wells 10 and 11 are negative controls with 0.5% BSA.
 Row B, wells 1-10 also contain a gradient of mSA standard solutions, and wells 11 and 12 are negative controls with 0.5% BSA.
-Row C, wells 1 and 4 are refolded samples of sGFP1-10 tether protein, while wells 2 and 5 are refolded samples of sGFP11 tether protein. Row D, well 1 contains purified samples of sGFP1-10 tether protein, and well 2 contains purified samples of sGFP11 tether protein.
+Row C, wells 1 and 4 are refolded samples of sGFP1-10 tether protein.
-Rows E and F, well 1 contains purified inclusion body samples of sGFP11 tether, and well 2 contains purified inclusion body samples of sGFP1-10 tether.
+Row D, well 1 contains purified samples of sGFP1-10 tether protein.
+Rows E and F, well 2 contains purified inclusion body samples of sGFP1-10 tether.
 </div></div></div></div>