Drug pipeline
Full profile accessExplore the programs pursuing this target and their development progress.
- Drug candidates
- Developers
- Development stage
Target intelligence / Profile preview
The SARS-CoV-2 B.1.351 spike glycoprotein is a trimeric, heavily glycosylated surface protein, consisting of S1 and S2 subunits. The S1 subunit includes the receptor-binding domain (RBD) containing key mutations (N501Y, K417N, E484K) that enhance binding affinity for the human ACE2 receptor and confer significant immune escape from neutralizing antibodies. This spike variant mediates viral entry by inducing membrane fusion upon ACE2 binding, and its structural changes increase both transmissibility and resistance to immune responses. Because of its essential role in infection and antigenicity, it is the main target for COVID-19 vaccines, diagnostics, and therapeutics, making it central to pandemic control efforts
Neutralizing antibodies bind spike protein, block ACE2 interaction; Protease inhibitors block S protein cleavage, preventing membrane fusion
2 more in the full profile.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Explore the programs pursuing this target and their development progress.
Follow the clinical studies evaluating therapies directed at this target.
Compare approaches across drug candidates, modalities, and indications.
Investigate the research and source evidence behind target biology and development.
Explore patent activity around therapies and technologies addressing this target.
Connect target biology, drug development, and emerging evidence in your research.
See how Gosset can support your research on SARS-CoV-2 spike glycoprotein (B.1.351 variant) (Spike protein (B.1.351); S protein (B.1.351); Beta spike protein).