Part:BBa_K3683000:Design
A universal platform with pseodoviruse of SARS-CoV-2
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 3094
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 1435
Illegal NgoMIV site found at 1951
Illegal NgoMIV site found at 2014
Illegal NgoMIV site found at 2509
Illegal NgoMIV site found at 2653
Illegal NgoMIV site found at 2686
Illegal NgoMIV site found at 2963 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 647
Illegal BsaI.rc site found at 898
Illegal BsaI.rc site found at 2558
Illegal SapI.rc site found at 915
Illegal SapI.rc site found at 1596
Design Notes
Production and titration of SARS-CoV-2 S pseudoviruses: to generate and culture either wild type SARS-CoV-2 S or S-D614G variant pseudotyped virus using a pair of cooresponding mutant primaers; Psuedovirus infection and neutralization; Authentic virus neutralization;
Source
The psPAX2 was purchased from addgene, and the pLOVE-Luciferase-EGFP was purchased from GenScript (Nanjing, China), the full length Spike gene (S) from the SARS-CoV-2 (previously 2019-nCoV) strain Wuhan-Hu-1 (GenBank: MN908947) was codon-optimized (sequence shown in Supplementary Table 1), synthesized, and cloned into pCAGGS vector (pCAGGS S(1-1254aa)) using seamless cloning by GenScript. The primers S-D614G-F, 5′-CTGTACCAGGgCGTGAATTGCACCGAGGTGC-3′ and S-D614G-R 5′- TGCAATTCACGcCCTGGTACAGCACGGCCACC-3′ were used to generate S-D614G mutant by PCR-based direct mutagenesis using High-fidelity DNA polymerase Mix (P525, Vazyme) with the following condition: 95℃ 5min, 95℃ 30s, 56℃ 30s, 72℃ 4min for 28 cycles, 72℃ 10min. We next purified the exact size of S-D614G PCR product by gel extraction, then we used Exnase II (C214, Vazyme) to make the linearized product circled. Then circled S-D614G plasmids were transformed into DH5α competent cells, single clones were select to grow recombinant plasmids in culture. The information for these maps are shown in Supplementary map.
References
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Hu et al, D614G mutation of SARS-CoV-2 spike protein enhances viral infectivity, BioRxiv, 2020, doi: https://doi.org/10.1101/2020.06.20.161323.
Yang et al, A vaccine targeting the RBD of the S protein of SARS-CoV-2 induces protective immunity, Nature. 2020 Jul 29. doi: 10.1038/s41586-020-2599-8.
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