Difference between revisions of "Part:BBa K4040015"
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<partinfo>BBa_K4040015 short</partinfo> | <partinfo>BBa_K4040015 short</partinfo> | ||
+ | ===Sequence and Features=== | ||
+ | <partinfo>BBa_K4040015 SequenceAndFeatures</partinfo> | ||
+ | ===Background and structure of CAR-MEGF10=== | ||
+ | The function of CAR-MEGF10 is the same as the CARγ, which increases the phagocytosis of the macrophages. And the structure is also highly similar to the CARγ, with the only difference lying in the intracellular domain of the CAR, in which the common γ subunit of Fc receptors is replaced by MEGF10. | ||
+ | ===The mechanism of CAR-MEGF10=== | ||
+ | To assay the library of CAR-Ps, previous study has introduced each CAR-P into J774A.1 murine macrophages by lentiviral infection. As an engulfment target, they used 5 mm diameter silica beads coated with a supported lipid bilayer. A His8-tagged extracellular domain of CD19 was bound to a NiNTA-lipid incorporated into the supported lipid bilayers. Macrophages expressing a CAR-P with the Megf10 (CAR-P Megf10) or FcRV (CAR-PFcRV ) intracellular domain promoted significant engulfment of CD19 beads compared to macrophages with no CAR (Figure 1, 2). | ||
+ | [[File:T--NMU_China--fig3b.png|thumb|center|600px|<b>Figure 1.</b> J774A.1 macrophages expressing aCD19 CAR-P with the indicated intracellular signaling domain (green) engulf 5 mm silica beads covered with a supported lipid bilayer containing His-tagged CD19 extracellular domain. The beads were visualized with atto390-labeled lipid incorporated into the supported lipid bilayer (magenta). Cells infected with the cell membrane marker, mCherry-CAAX, were used as a control (no CAR, top left). To the right of each image is a histogram depicting the frequency of cells engulfing the indicated number of beads.]] | ||
+ | [[File:T--NMU_China--fig3c.png|thumb|center|350px|<b>Figure 2.</b> The average number of beads eaten per cell.]] | ||
− | + | More information can be found in Intracellular Domain of the MEGF10 Protein(<partinfo>BBa_K4040000</partinfo>). | |
− | + | ===Results of our project=== | |
+ | Please find it out in CAR-MERTK(<partinfo>BBa_K4040018</partinfo>). | ||
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===Usage and Biology=== | ===Usage and Biology=== | ||
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Latest revision as of 13:04, 15 October 2021
CAR-MEGF10
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal XhoI site found at 344
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 952
Illegal NgoMIV site found at 1288
Illegal NgoMIV site found at 1825
Illegal NgoMIV site found at 1891
Illegal NgoMIV site found at 2050
Illegal AgeI site found at 440 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 1168
Illegal BsaI.rc site found at 1432
Illegal SapI.rc site found at 1989
Illegal SapI.rc site found at 2619
Background and structure of CAR-MEGF10
The function of CAR-MEGF10 is the same as the CARγ, which increases the phagocytosis of the macrophages. And the structure is also highly similar to the CARγ, with the only difference lying in the intracellular domain of the CAR, in which the common γ subunit of Fc receptors is replaced by MEGF10.
The mechanism of CAR-MEGF10
To assay the library of CAR-Ps, previous study has introduced each CAR-P into J774A.1 murine macrophages by lentiviral infection. As an engulfment target, they used 5 mm diameter silica beads coated with a supported lipid bilayer. A His8-tagged extracellular domain of CD19 was bound to a NiNTA-lipid incorporated into the supported lipid bilayers. Macrophages expressing a CAR-P with the Megf10 (CAR-P Megf10) or FcRV (CAR-PFcRV ) intracellular domain promoted significant engulfment of CD19 beads compared to macrophages with no CAR (Figure 1, 2).
More information can be found in Intracellular Domain of the MEGF10 Protein(BBa_K4040000).
Results of our project
Please find it out in CAR-MERTK(BBa_K4040018).