Difference between revisions of "Part:BBa K4122014"
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<h3>Characterization-Introduction of Tag-Catcher system to co-display PETase and MHETase</h3> | <h3>Characterization-Introduction of Tag-Catcher system to co-display PETase and MHETase</h3> | ||
+ | <p>In this assembly, GFP is a green fluorescent protein, showing green fluorescence, His-tag is used for protein purification, and Spytag will form a tight connection with spycatcher, which in turn anchors the attached GFP to the cell surface.Promoter-PFBA1, Terminator-TADH2.</p> | ||
<P>To attain co-display, we combined our display system with two selective protein binding systems, SpyTag-SpyCatcher and SnoopTag-SnoopCatcher. | <P>To attain co-display, we combined our display system with two selective protein binding systems, SpyTag-SpyCatcher and SnoopTag-SnoopCatcher. |
Latest revision as of 08:12, 6 October 2022
PFBA1-SP-GFP-His-Spytag-TADH2
Characterization-Introduction of Tag-Catcher system to co-display PETase and MHETase
In this assembly, GFP is a green fluorescent protein, showing green fluorescence, His-tag is used for protein purification, and Spytag will form a tight connection with spycatcher, which in turn anchors the attached GFP to the cell surface.Promoter-PFBA1, Terminator-TADH2.
To attain co-display, we combined our display system with two selective protein binding systems, SpyTag-SpyCatcher and SnoopTag-SnoopCatcher. In our experiment, GFP and RFP were used to indicate the successful construction of Spycatcher/Spytag and Snoopcatcher/Snooptag systems. We initially tried two catcher types with a ratio of 1:3.
Fig.1 The construction of plasmid Ts-PGAPDH--TENO1A, the surface display system for displaying both GFP and RFP. (BBa_K4122017)
SC: Spycatcher BBa_K4122008; SNC: Snoopcatcher BBa_K4122010; V5: V5 tag BBa_K3829004; CBM: carbohydrate binding domain BBa_K4122006
GFP+ and RFP+ suggested the successful construction of Spycatcher/Spytag system and Snoopcatcher/Snooptag system.
Fig.2 The fluorescence result of the spy/snoop tag and catcher system.
A and D, bright field; B and E, Green fluorescence; C and F, Red fluorescence
References
[1] Wei Zheng, Chengxin Zhang, Yang Li, Robin Pearce, Eric W. Bell, Yang Zhang. Folding non-homology proteins by coupling deep-learning contact maps with I-TASSER assembly simulations. Cell Reports Methods, 1: 100014 (2021).
[2] Chengxin Zhang, Peter L. Freddolino, and Yang Zhang. COFACTOR: improved protein function prediction by combining structure, sequence and protein-protein interaction information. Nucleic Acids Research, 45: W291-299 (2017).
[3] Jianyi Yang, Yang Zhang. I-TASSER server: new development for protein structure and function predictions, Nucleic Acids Research, 43: W174-W181, 2015.
[4] Lu, Hongyuan, et al. "Machine learning-aided engineering of hydrolases for PET depolymerization." Nature 604.7907 (2022): 662-667.
Sequence and Features