Recombinant SARS-CoV-2 Stabilized Spike Glycoprotein, His/Strep-tagged
Specification
Related Products
| Cat#: |
HUM-386 |
| Product Name: |
Recombinant SARS-CoV-2 Stabilized Spike Glycoprotein, His/Strep-tagged |
| Description: |
SARS-CoV-2 Stabilized Spike (full-length) is a recombinant antigen which contains 6 mutations in S2 which stabilises the protein as a pre-fusion trimer. The protein was produced according to Hsieh et al. in HEK293 cells and purified from culture supernatant by affinity chromatography. SARS-CoV-2, previously known as the 2019 Novel Coronavirus (2019-nCoV), causes the pandemic COVID-19 disease. |
| Gene: |
Spike Glycoprotein |
| Species: |
SARS-CoV-2 |
| Source: |
HEK293 |
| Synonyms: |
SARS-CoV-2 Stabilized Spike Glycoprotein |
| Formulation: |
DPBS |
| Purity: |
~95% purity. |
| Notes: |
This product is intended for research and manufacturing uses only. It is not a diagnostic device. The user assumes all responsibility for care, custody and control of the material, including its disposal, in accordance with all regulations. |
| Tags: |
His/Strep |
| Background: |
SARS-CoV-2 is a novel betacoronavirus and the causative agent of the COVID-19 pandemic. Coronavirus virions are covered with a spike (S) glycoprotein that binds to host-cell receptors and mediates cell entry via fusion of the host and viral membranes. Binding of the SARS-CoV-2 spike to the angiotensin-converting enzyme 2 (ACE2) receptor triggers a large conformational rearrangement of the spike from a metastable prefusion conformation to a highly stable post fusion conformation, facilitating membrane fusion. Attachment and entry are essential for the viral life cycle, making the S protein a primary target of neutralizing antibodies and an important vaccine antigen.
Recombinant expression yields of viral fusion glycoproteins has been found to be improved by prefusion stabilization, possibly by preventing triggering or misfolding that results from a tendency to adopt the more stable post fusion structure. They are also better immunogens compared to their wild-type counterparts (Pallesen et al. 2017). These variants (S-2P) contain two consecutive proline substitutions in the S2 subunit and these S2-P spikes have produced high-resolution structures by cryo-EM for SARS-CoV-2. However, even with these substitutions, the SARS-CoV-2 S-2P ectodomain is still unstable and difficult to produce reliably in mammalian cells (Walls et al., 2020; Wrapp et al., 2020).
Recently, a more stable construct (designated HexaPro), has been designed, combining multiple proline substitutions (F817P, A892P, A899P, A942P and the S-2P mutations, K986 and V987) and resulting in substantial increases in expression and stability. Large-scale HexaPro preparations retain a monodisperse SEC peak corresponding to the molecular weight of a glycosylated trimer and are indistinguishable from S-2P by negative stain EM. HexaPro expressed 9.8-fold higher than S-2P, had ~5 centigrade increase in Tm, and retained the trimeric prefusion conformation. In addition, the binding kinetics of HexaPro to the human ACE2 receptor were shown to be comparable to those of S-2P. It remained folded in the prefusion conformation after 3 cycles of freeze-thaw, 2 days incubation at room temperature or 30 min at 55 centigrade. HexaPro also reacts to human convalescent sera and RBD-specific mAb (CR3022) (Yuan et al., 2020) similarly to S-2P, suggesting its antigenicity is well-preserved. Collectively, these data support HexaPro as a promising candidate for SARS-CoV-2 vaccine and diagnostic development (Hsieh et al., 2020). |
For research use only. Not intended for any clinical use. No products from Creative BioMart may be resold, modified for resale or used to manufacture commercial products without prior written approval from Creative BioMart.
