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. 2022 Sep 19;12:15668. doi: 10.1038/s41598-022-19886-y

Figure 1.

Figure 1

Expression and purification of recombinant spike subunit fragments of SARS-CoV-2 and SARS-CoV. (A) Structure features of the SARS-CoV-2 spike (S) protein and the flow chart of protein library construction were generated by Microsoft PowerPoint 2016. The listed domain boundaries are mostly defined according to NTD, N Terminal Domain; RBD, Receptor Binding Domain; FP, Fusion Peptide; HR1, Heptad Repeat 1; HR2, Heptad Repeat 2; TM, Transmembrane Domain; CT, Cytoplasmic Tail. (For visual clarity, the length of the boxes is not proportional to the real sequence length). (B) Amino acid location and molecular weight of the protein fragments. (C and D) Twelve protein fragments expressing plasmids of SARS-CoV-2 and SARS-CoV were constructed and verified by agarose gel electrophoresis with restriction enzymes BamH I and Hind III. M: DNA markers of known size. Lane1-6: COVID19-SF1-6 (C) and SARS-SF1-6 (D). (E and F) SDS-PAGE analysis of the protein fragments expression of SARS-CoV-2 and SARS-CoV, respectively. M: Prestained protein markers of known size. Lane1-6: COVID19-SF1-6 (E) and SARS-SF1-6 (F).